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Review

Molecular Mechanisms of Parathyroid Disorders in Chronic Kidney Disease

by
Alia Hassan
1,
Nareman Khalaily
1,
Rachel Kilav-Levin
1,2,
Morris Nechama
3,4,
Oded Volovelsky
3,4,
Justin Silver
1 and
Tally Naveh-Many
1,4,*
1
Minerva Center for Bone and Mineral Research, Nephrology Services, Hadassah—Hebrew University Medical Center, Jerusalem 91120, Israel
2
Nursing, Jerusalem College of Technology, Jerusalem 91160, Israel
3
Pediatric Nephrology, Hadassah—Hebrew University Medical Center, Jerusalem 91120, Israel
4
The Wohl Institute for Translational Medicine, Hadassah—Hebrew University Medical Center, Jerusalem 91120, Israel
*
Author to whom correspondence should be addressed.
Metabolites 2022, 12(2), 111; https://0-doi-org.brum.beds.ac.uk/10.3390/metabo12020111
Submission received: 28 December 2021 / Revised: 17 January 2022 / Accepted: 20 January 2022 / Published: 25 January 2022
(This article belongs to the Special Issue Frontiers in Bone Metabolism and Disorder in Chronic Kidney Disease)
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Abstract

:
Secondary hyperparathyroidism (SHP) is a common complication of chronic kidney disease (CKD) that induces morbidity and mortality in patients. How CKD stimulates the parathyroid to increase parathyroid hormone (PTH) secretion, gene expression and cell proliferation remains an open question. In experimental SHP, the increased PTH gene expression is post-transcriptional and mediated by PTH mRNA–protein interactions that promote PTH mRNA stability. These interactions are orchestrated by the isomerase Pin1. Pin1 participates in conformational change-based regulation of target proteins, including mRNA-binding proteins. In SHP, Pin1 isomerase activity is decreased, and thus, the Pin1 target and PTH mRNA destabilizing protein KSRP fails to bind PTH mRNA, increasing PTH mRNA stability and levels. An additional level of post-transcriptional regulation is mediated by microRNA (miRNA). Mice with parathyroid-specific knockout of Dicer, which facilitates the final step in miRNA maturation, lack parathyroid miRNAs but have normal PTH and calcium levels. Surprisingly, these mice fail to increase serum PTH in response to hypocalcemia or uremia, indicating a role for miRNAs in parathyroid stimulation. SHP often leads to parathyroid hyperplasia. Reduced expressions of parathyroid regulating receptors, activation of transforming growth factor α-epidermal growth factor receptor, cyclooxygenase 2-prostaglandin E2 and mTOR signaling all contribute to the enhanced parathyroid cell proliferation. Inhibition of mTOR by rapamycin prevents and corrects the increased parathyroid cell proliferation of SHP. This review summarizes the current knowledge on the mechanisms that stimulate the parathyroid cell at multiple levels in SHP.

1. Introduction

Parathyroid hormone (PTH) regulates serum calcium and phosphate levels and bone strength. A reduction in serum calcium stimulates PTH secretion and, when prolonged, parathyroid cell proliferation [1,2,3]. A 7-transmembrane G-protein-coupled calcium-sensing receptor (CaSR) senses changes in extracellular serum calcium. Increased calcium activates the parathyroid CaSR, leading to decreased PTH secretion [4,5,6]. Other factors that act on the parathyroid are serum phosphate that stimulates and vitamin D and the bone-derived phosphaturic hormone fibroblast growth factor 23 (FGF23) that suppress PTH synthesis, secretion and proliferation [7,8,9,10]. A recent study suggested that the CaSR also acts as a phosphate sensor in the parathyroid gland. According to this study, phosphate increases PTH secretion by inhibiting the CaSR in a noncompetitive manner [11]. The active metabolite of vitamin D, 1,25-dihydroxy-vitamin D (1,25D), suppresses PTH gene transcription. It binds to the vitamin D receptor (VDR), which heterodimerizes with retinoic acid X receptors. The complex then enters the nucleus to bind vitamin D-response elements in the PTH gene promoter region [12,13,14,15]. FGF23 acts on the FGFR1-klotho receptor complex, expressed in the parathyroid, to decrease PTH expression [9,16]. Secondary hyperparathyroidism (SHP) is a common complication of chronic kidney disease (CKD) that correlates with morbidity and mortality in these patients. SHP is characterized by increased PTH gene expression and secretion and parathyroid gland hyperplasia [17,18,19,20]. Many factors combine to form SHP in CKD. These include phosphate retention, hyperphosphatemia, hypocalcemia and low levels of 1,25D. In addition, parathyroid gland hyperplasia leads to reduced expression of the VDR, CaSR and FGF23 receptor complex in experimental SHP models and human parathyroid samples [3,19,21]. Other parathyroid post-receptor mechanisms also affect PTH expression and parathyroid cell proliferation. The magnitude of SHP is determined by two major mechanisms, an increase in PTH synthesis and an increase in parathyroid gland mass [22]. Parathyroid cells have a limited number of secretory granules containing preformed hormone compared to other endocrine cells. Therefore, increases in PTH gene expression are essential for a continued secretion of PTH. The increased PTH gene expression in experimental SHP induced by either uremia or prolonged hypocalcemia is due to post-transcriptional mechanisms that alter PTH mRNA stability and levels [23,24,25,26].

2. Post-Transcriptional Mechanisms Regulating Parathyroid Hormone Gene Expression in Secondary Hyperparathyroidism

2.1. Regulation of PTH mRNA Stability by Protein–PTH mRNA Interactions and Pin1

The balance between the rates of gene transcription and mRNA decay determines cytoplasmic levels of all mRNAs. mRNA decay is tightly regulated by mRNA-binding proteins that bind to specific sequences in mRNAs [27,28,29]. In most mRNAs, these sequences are adenosine-uridine (AU)-rich elements (AREs) embedded in the 3′-untranslated region (UTR) [28,30,31,32,33,34]. AU-rich binding factor 1 (AUF1, HNRNPD gene product) and K-homology splicing regulatory protein (KSRP) are two mRNA-binding proteins that bind ARE containing mRNA 3′-UTRs [28,30,31,35]. AUF1 promotes either decay or stability, depending on the cell type and mRNA [36,37]. KSRP induces mRNA decay by recruiting the multi-subunit RNA ribonuclease complex, exosome to the mRNA 3′ ends [38]. Post-translational modifications of the mRNA-binding proteins affect protein–mRNA interactions [35,39,40,41,42,43]. Post-transcriptional regulatory mechanisms of thr mRNA binding proteins contribute to the regulation of gene expression in a wide variety of cellular and physiological processes, including hormones. Insulin and insulin-like growth factor expression, as well as the expression of different reproductive hormones is regulated by gene transcription as well as changes in mRNA stability, localization and mRNA translation efficiency [44,45,46,47]. Post-transcriptional mechanisms also mediate the increased PTH gene expression by hypocalcemia and uremia in SHP [48].
Enhanced PTH mRNA stability is the major mechanism that increases PTH gene expression in experimental SHP due to either dietary induced prolonged hypocalcemia or uremia. Increased PTH mRNA binding to stabilizing AUF1 and decreased binding to the decay-promoting protein KSRP shifts the balance towards increased PTH mRNA stability and levels [23,24,25]. These proteins bind to an evolutionary conserved ARE in the PTH mRNA 3′-UTR [49] (Figure 1). The peptidyl prolyl cis/trans isomerase Pin1 coordinates the interaction of these ARE binding proteins to the PTH mRNA. Pin1 specifically binds phosphorylated serine/threonine-proline motifs in target proteins and induces conformational changes of the peptidyl bond [50,51]. By inducing conformational changes, Pin1 controls the activity of many phosphoproteins in a wide range of cellular activities [52,53]. Pin1 also binds RNA-binding proteins, including AUF1 and KSRP, to regulate the stability of ARE containing mRNAs that include GM-CSF, TGF-β1 and PTH [53,54,55,56]. During oocyte maturation, Pin1 binds phosphorylated cytoplasmic polyadenylation element binding (CPEB) protein that regulates mRNA translation through cytoplasmic polyadenylation. This leads to CPEB isomerization and subsequent degradation in a ubiquitination-dependent manner [57,58]. In the parathyroid, Pin1 induces PTH mRNA decay by altering KSRP phosphorylation and KSRP-PTH mRNA binding [54,59]. Pin1-KSRP interaction leads to Pin-dependent KSRP conformational change that leads to dephosphorylation of KSRP at Ser181. Un-phosphorylated KSRP then binds PTH mRNA with higher affinity, inducing PTH mRNA decay. This regulation of PTH mRNA stability and levels by Pin1 is dependent upon the PTH mRNA 3′-UTR ARE. In SHP, Pin1 isomerase activity is decreased and phosphorylated KSRP fails to bind PTH mRNA, resulting in increased PTH mRNA and serum levels. In accordance, pharmacologic inhibition of Pin1 increased PTH mRNA levels post-transcriptionally in vivo, in rat parathyroid glands in culture and in transfected cells. Furthermore, Pin1−/− mice have increased serum PTH and PTH mRNA levels [54]. Therefore, Pin1 decreased activity, parathyroid Pin1-KSRP interaction and KSRP-PTH mRNA binding play a significant role in the regulation of PTH mRNA stability and in the pathogenesis of the SHP (Figure 1 and Figure 2).
Recently, mRNA profiles of porcine parathyroid glands were performed in a long-term dietary phosphorus intervention by keeping pig offspring on distinct mineral dietary phosphorus levels throughout fetal and postnatal life. RNA sequencing data and the resulting molecular pathways of parathyroid glands showed that PTH abundance is controlled via Pin1, CaSR, MAfB, Phospholipase C and proteinase A signaling to regulate PTH gene expression, stability and secretion. Parathyroid glands revealed lowered Pin1 mRNA abundance in animals fed a low phosphorus diet with no change in the expression of KSRP by post-weaning diets [60].
In patients with diffuse and nodular hyperparathyroidism, normal and hyperplastic human parathyroid tissue microarrays showed that AUF1 was among the differentially expressed genes [61]. We analyzed the publicly deposited mRNA profiling data from a study comparing adenomas to normal human parathyroid tissues (NCBI Gene Expression Omnibus accession number GSE83421) [62]. We found that Pin1 mRNA was 30% higher (p < 0.01) in parathyroid adenomas vs. normal parathyroid tissues. Additional proteins that were related to RNA stability as well as protein synthesis and processing, DNA repair and cell growth were also dysregulated [26]. In another human study of single nucleotide polymorphisms (SNP) in the Pin1 gene promoter, in the Chinese Han population in Northwest China, Pin1 C667T genetic variants were associated with CKD SHP. They suggested that the Pin1 variant genotypes may be used as biomarkers for susceptibility to CKD SHP [63]. Together, these studies support a role for Pin1 and PTH mRNA interacting proteins not only in experimental models, but also in human SHP patients.

2.2. Parathyroid microRNA Ablation in Experimental Secondary Hyperparathyroidism

MicroRNAs (miRNAs) provide an additional post-transcriptional mechanism of gene expression. miRNAs are short endogenous non-coding RNAs that affect gene expression by inducing sequence-specific mRNA decay and/or translation repression of target mRNAs [64,65]. miRNAs are transcribed as primary (pri)-miRNA transcripts that are first cleaved by nuclear Drosha and then by Dicer in the cytoplasm to generate the mature miRNA [66]. Hence, Dicer is essential for the formation of mature and functional miRNAs. Mice deficient in Dicer die at embryonic day E8.5 [67]. However, tissue-specific Dicer knockout mice are useful to study the role of miRNAs in a particular tissue [68,69,70]. To study the role of miRNAs in the parathyroid, we generated mice with parathyroid-specific gene deletion of Dicer (PT-Dicer−/− mice). The PT-Dicer−/− mice developed normally and had normal basal serum PTH, calcium and phosphate levels. Remarkably, the PT-Dicer−/− mice failed to increase serum PTH after the stimuli of acute and chronic hypocalcemia. Moreover, the PT-Dicer−/− mice also failed to increase serum PTH levels when stressed by an adenine high phosphorus diet to induce CKD [48,71]. Therefore, intact Dicer and miRNAs are essential for activation of the parathyroid by the major stimuli for PTH secretion, acute and chronic hypocalcemia and uremia (Figure 2).

2.3. Parathyroid miRNA Profiles

Differentially expressed miRNAs have been described in primary hyperparathyroidism of adenomas and carcinoma patients, compared to normal parathyroid tissue [72,73,74,75,76]. Studies in parathyroid carcinomas identified miRNAs that were downregulated when compared to controls, and are common to other human cancers [77,78]. Interestingly, parathyroid carcinomas showed deregulation of miRNAs belonging to the largest human chromosome 19 miRNA cluster [79]. Downregulation of miR-296-5p was the best predictor in differentiating parathyroid carcinomas from normal parathyroids [80].
In contrast to parathyroid carcinoma and adenoma, parathyroid miRNA profiles of SHP where less studied. We performed the first study of miRNA expression and function in normal parathyroid physiology and in SHP, by applying small RNA sequencing, providing quantitative global miRNA profiling. We compared parathyroid tissue from control and end-stage renal disease SHP patients, as well as experimental SHP models. Of interest, there was similar miRNA content in the 50 most frequent miRNA families of normal parathyroid glands from humans and rodents. Let-7 miRNA family members were the most highly expressed miRNAs in human, mouse and rat parathyroids, followed by miR-30 and miR-141/miR-200 family members [81]. SHP correlated with substantial miRNA transcriptome (miRNome) alterations. miRNA levels were substantially dysregulated by miRNA sequencing in both hyperplastic parathyroid glands from ESRD patients and parathyroid glands from rats fed an adenine high-phosphorus diet to induce CKD and SHP, indicating that miRNAs may be involved in the pathogenesis of CKD-SHP. Analysis of the highest expressed dysregulated miRNAs in adenine high phosphorus-induced SHP rats showed a common pattern, in which a miRNA sequence family is either upregulated or downregulated in early renal failure and the trend is increased in late CKD. miR-141 and miR-148 members both increased, peaking gradually by 8 weeks of the adenine diet-induced CKD [81]. The conservation through evolution of miRNA expression in normal parathyroids and the dysregulation of miRNAs in SHP in man, mouse and rat suggests their functional and developmental importance in SHP.

2.4. Function of Individual miRNAs in PTH Expression

We used anti-miR oligonucleotides, that compete with cellular target mRNAs for the binding of endogenous miRNA, to study the role of specific miRNAs in SHP [82]. We chose to inhibit let-7 members, as these are the most abundant miRNA molecules in the parathyroid and individual let-7 members were significantly dysregulated in both rat and human SHP [81]. Anti-let-7 oligonucleotides nearly doubled serum PTH levels in normal rats, and worsened SHP in uremic rats, compared to scrambled control oligonucleotides. The increased serum PTH levels observed by let-7 inhibition did not affect serum phosphate, calcium or creatinine in normal and uremic rats, suggesting a direct effect of the anti-miRs on PTH levels. Let-7 anti-miRs also increased PTH secretion in vitro, when added to normal mouse thyro-parathyroid glands in culture, confirming a primary effect of let-7 antagonism on PTH production and/or secretion in vivo in control and uremic rats and in vitro [81].
We also antagonized miR-148 and miR-141 because of the high abundance of these miRNAs in human, rat and mouse parathyroid glands and their increase in SHP. Anti miR-141 had no effect on PTH expression. However, anti miR-148 significantly decreased serum PTH levels in uremic rats, again with no change in serum creatinine or phosphate levels. Adding anti-miR-148 to thyro-parathyroid tissue from uremic mice, compared with control oligonucleotides, also decreased PTH secretion in vitro, demonstrating a direct effect of antagonizing miR-148 on the parathyroid [81]. Therefore, specific miRNA families are dysregulated in CKD-SHP. Inhibition of let-7 and miR-148 modifies PTH secretion in vivo and in vitro, suggesting roles for these miRNAs in PTH expression (Figure 2).

3. Parathyroid Cell Proliferation in Secondary Hyperparathyroidism

The increase in PTH gene expression is tightly linked to increased parathyroid mass due to parathyroid cell proliferation and, to a lesser extent, an increase in cell size. The molecular pathways mediating parathyroid cell proliferation are still unclear. The parathyroid cells are generally quiescent under physiological conditions, with a low turnover rate and mitoses [83]. However, the cells retain their potential to proliferate in response to uremia, hypocalcemia, hyperphosphatemia and vitamin D deficiency [84]. In CKD patients, at the early stages of SHP, the parathyroid glands show diffuse and polyclonal proliferation. Prolonged uremia drives the progression of parathyroid cell proliferation from diffuse to nodular growth [85,86]. The main factors responsible for parathyroid hyperplasia are similar to those that increase PTH biosynthesis and secretion. High phosphate, hypocalcemia and 1,25D deficiency in CKD all contribute to the development of hyperplasia [87].The studies on parathyroid cell proliferation in experimental SHP of renal failure mainly rely on either 5/6 nephrectomy performed by removing one kidney and 2/3 of the contralateral kidney or an adenine diet. SHP is further increased when the rodents in these models are fed a high phosphorus diet [7,17,18,88,89,90,91]. In both experimental models and in patients, the downregulation of CaSR and VDR expression is associated with parathyroid cell proliferation. The decrease in parathyroid CaSR occurs in CKD only when the parathyroid glands are hyperplastic, and may contribute to the increased parathyroid proliferation in SHP [92,93,94,95,96]. Phosphate restriction prevents both parathyroid hyperplasia and the decreased CaSR expression in CKD. Uremic patients with SHP, as well as rodents with experimental SHP, have decreased VDR mRNA and protein levels [21,93,97,98]. These and other studies suggested that parathyroid gland hyperplasia reduces expression of both the CaSR and VDR, which further contributes to the high PTH secretion and parathyroid cell proliferation in SHP (Figure 3).
The classical treatment for SHP patients included active vitamin D compounds and phosphate binders, to limit gastrointestinal phosphate absorption [100]. Administration of vitamin D to rats with secondary hyperparathyroidism reduced parathyroid cell proliferation and increased both VDR and CaSR expression [17,101,102]. However, while vitamin D compounds suppress PTH secretion, they also promote calcium and phosphate intestinal absorption. Calcimimetic compounds are positive allosteric modulators of the CaSR that increase the sensitivity of the CaSR, thereby decreasing PTH secretion. Calcimimetics lower PTH levels in CKD patients with SHP. Studies using experimental CKD rat models have demonstrated that calcimimetics reduce parathyroid hyperplasia, as measured by gland weight, DNA content and staining for proliferation markers [103]. Reduction in parathyroid gland volume has also been demonstrated using imaging studies in dialysis patients receiving calcimimetic [94,104]. Calcimimetics increase cell surface CaSR and VDR expression in the parathyroid cells in uremic rats [105]. The calcimimetic R568 also reduced PTH gene expression in CKD rats by decreasing PTH mRNA stability through increased parathyroid KSRP–PTH mRNA interactions compared to untreated CKD rats [106].

3.1. Cell Cycle Regulation

Two particular genes have been implicated in the pathogenesis of parathyroid tumorigenesis: the cyclin D1/PRAD1 (Cyclin parathyroid adenomatosis 1) oncogene and the MEN1 (multiple endocrine neoplasia type 1) tumor-suppressor gene [107,108]. Menin, the product of the MEN1 gene, is a tumor suppressor protein in a variety of cancer types. Inactivating MEN1 mutations lead to the development of parathyroid neoplasia in almost all patients with MEN1 [109]. PRAD1, later identified as cyclin D1, plays a vital role in controlling the cell cycle [110]. Cyclin D1 protein overexpression occurs in 20–40% of parathyroid adenomas, suggesting that increased PRAD1/cyclin D1 is one of the genetic abnormalities responsible for tumorigenesis in sporadic primary parathyroid adenomas, contributing to parathyroid hyperplasia in humans [110,111,112]. In about 8% of cases, there is DNA rearrangement involving the cyclin D encoding CCND1 gene locus [113]. Transgenic mice with parathyroid-targeted overexpression of cyclin D1, modeling the gene rearrangement found in human tumors, showed that a primary defect in this cell-cycle regulator caused primary hyperparathyroidism, as in human patients [114,115]. These findings suggest that overexpression of the cyclin D1 oncogene drives excessive parathyroid cell proliferation.
The roles of mutations in cyclin D1 and MEN1 in SHP are not entirely understood. The levels of cyclin D1 and retinoblastoma gene products increase in CKD-induced hyperplastic parathyroid cells [116]. The increase in cell cycle progression in SHP correlates with a decrease in the expression of the cyclin-dependent kinase inhibitors, p21 and p27 (Figure 3). Loss of expression or function of p21 and p27 is implicated in many human malignancies [117]. The decrease in parathyroid p21 and p27 levels in SHP are most evident in cells with nodular hyperplasia. Low dietary phosphorus reduced parathyroid cell proliferation in SHP rats, together with induction of p21, and reduced expression of transforming growth factor (TGF)-α expression. A high phosphorous intake, with subsequent stimulation of parathyroid cell proliferation in 5/6 nephrectomized rats, increased TGF-α [118]. 1,25D, which prevented parathyroid gland hyperplasia in uremic rats, enhanced parathyroid p21 expression and prevented the high phosphorus-induced increase in parathyroid TGF-α content [119]. In addition, 1,25D alters membrane trafficking of the epithelial growth factor receptor (EGFR), which binds both EGF and TGF-α and downregulates EGFR-mediated growth signaling [120].

3.2. TGF-α and EGFR

TGF-α and its receptor EGFR are increased in uremic rats and human hyperplastic and adenomatous parathyroid glands correlating with parathyroid cell proliferation [121,122] (Figure 3). EGFR signals through MAPK activation, which in turn induces cyclin D1 and drives the cell cycle from G1 to S [122,123,124]. EGFR activation by TGF-α also reduces VDR expression and plays an important role in growth of the parathyroid gland. Inhibition of parathyroid TGF-α/EGFR prevents not only parathyroid cell proliferation, but also the reduction in VDR levels in parathyroid cells. In transgenic mice, a parathyroid-specific dominant-negative EGFR prevented the increase in serum PTH, parathyroid gland size and the decreased VDR expression observed in wild-type uremic mice [125]. EGFR also activates the AKT-mTORC1 (mammalian target of rapamycin complex 1) pathway [126,127].

3.3. The mTORC1 Pathway

mTOR integrates signaling pathways to regulate cell growth and proliferation. mTOR is part of mTORC1 and mTORC2. mTORC1 senses extracellular nutritional and growth factors necessary for cell growth and proliferation [128]. Rapamycin inhibits mTORC1 and cell proliferation. Different stimuli activate mTORC1 through Akt phosphorylation [129]. 4E binding protein 1 and the ribosomal protein S6 kinase 1 (S6K1) are mTORC1 targets. Upon activation, S6K1 phosphorylates its downstream target ribosomal protein S6 (rpS6) on a cluster of five serine residues at the carboxy terminus [130,131]. Knock-in mice encoding a mutant rpS6 harboring alanine substitutions at all serine phosphorylation sites (rpS6p−/− mice) have reduced body size, glucose intolerance and muscle weakness and impaired renal hypertrophy after uni-nephrectomy [132,133]. We have shown that the mTOR pathway is activated in the parathyroids of rats and mice with SHP induced by either chronic hypocalcemia or uremia. The increased mTOR activity correlated with increased parathyroid cell proliferation (Figure 3). Inhibition of mTORC1 by rapamycin both prevented and decreased parathyroid cell proliferation in SHP rats and in vitro in uremic rat parathyroid glands in organ culture. Knock-in rpS6p−/− mice had a muted increase in PTH secretion after induction of experimental CKD by an adenine high phosphorus diet and no increase in parathyroid cell proliferation, compared with the expected increases in uremic wild-type mice [134]. These results highlight the essential role of mTORC1 activation by rpS6 phosphorylation in parathyroid cell proliferation and in the pathogenesis of SHP. EGFR activates the AKT-mTORC1 pathway; therefore, the mTORC1 and EGFR pathways may act together to stimulate parathyroid cell proliferation in SHP [99] (Figure 3).

3.4. Nuclear Factor-Kappa B

As described above, reduced circulating 1,25D and parathyroid VDR expression play a key role in the progression of parathyroid hyperplasia. 1,25D administration partially restores parathyroid VDR expression and suppresses parathyroid cell proliferation by binding to its receptor [102]. In renal tubular cells, VDR binds to nuclear factor kappa B (NF-kB) dimers to suppress NF-κB-mediated gene transcription [135]. NF-κB is a ubiquitous transcription factor that plays a crucial role in immune and inflammatory responses. It consists of the DNA binding subunit p50 and the transactivation subunit p65/RelA (p65) [136]. In most cells, NF-kB is sequestered in the cytoplasm bound to its biological inhibitor IkB. A variety of stimuli, such as cytokines, toxins and mitogens, activate the IkB kinase complex leading to the degradation of phosphorylated IkB and the release and nuclear translocation of NF-kB [137]. Cyclin D1 is potently activated by p65 [138]. The tumor suppressor gene menin interacts with NF-kB and inhibits the NF-kB-mediated transcriptional activation [139]. NF-κB contributes to the pathogenesis of primary parathyroid hyperplasia [140]. In CKD-induced SHP, there was activation of the NF-κB pathway in the nodular hyperplastic parathyroid glands from patients on dialysis, with a significant increase in diffuse hyperplasia glands [141]. The reduction in VDR could lead to activation of the NF-κB pathway. In 5/6 nephrectomized rats fed a high-phosphorus diet, proliferation was higher together with activation of the NF-κB pathway, and VDR levels were decreased as expected, compared with the sham group. 1,25D decreased serum PTH and parathyroid cell proliferation, together with reduced activation of the NF-κB pathway [141]. These findings suggest that NF-κB contributes to parathyroid gland hyperplasia progression in SHP. Decreased 1,25D and VDR expression may affect parathyroid gland hyperplasia through the activation of the NF-κB pathway.

3.5. Cyclooxygenase 2-PGE2

Cyclooxygenase (COX) catalyzes the rate-limiting step of prostaglandin synthesis from arachidonic acid. Cox1 is constitutively expressed, while COX2 is induced by various mitogenic and inflammatory stimuli [142]. COX2 plays a significant role in carcinogenesis by promoting cell proliferation, inhibiting apoptosis and stimulating angiogenesis. COX2 is expressed in parathyroid cells of normal, hyperplastic and adenomatous parathyroid glands [143]. In end-stage renal disease patients with advanced SHP, there was enhanced expression of both COX2 and its downstream metabolic product prostaglandin E2 (PGE2) in their parathyroids [144]. Increased COX2 expression was also reported in parathyroids of 5/6-nephrectomized rats fed a high-phosphorus diet, together with the high PTH levels, parathyroid size and cell proliferation, compared to controls. Addition of PGE2 increased PTH production in dispersed primary human and bovine parathyroid cells [145,146]. In primary cultures of parathyroid glands isolated from end-stage renal disease patients, high phosphate increased PTH secretion, parathyroid cell proliferation and COX2 activity. Inhibitors of the PGE2 receptor 2 subtype (EP2) attenuated hyperparathyroidism induced by high phosphate. PGE2 or EP2 agonist directly stimulated hyperparathyroidism, suggesting that COX2 downstream PGE2 and its receptor EP2 play a role in the high phosphate-induced parathyroid hyperplasia of SHP [147] (Figure 3).

3.6. The Parathyroid Molecular Circadian Clock

Circadian rhythms act in metabolism, hormone secretion, cell cycle and locomotor activity. They are regulated by the molecular circadian clock, with the master clock in the suprachiasmatic nucleus of the central nervous system. In addition, internal clocks are expressed in several peripheral tissues. PTH secretion exhibits a diurnal variation and PTH gene promoter contains an E-box-like element in both humans and rodents, that is a target of circadian clock proteins [148,149]. A recent study by Egstrand and colleagues describes an internal operating molecular circadian clock in the parathyroid gland, which is disturbed in chronic kidney disease [150]. Because disturbed circadian rhythm may lead to abnormal growth, Egstrand and colleagues studied the expression of parathyroid clock and clock-regulated cell cycle genes in parathyroid glands of normal and CKD rats. They found that circadian clock genes were rhythmically expressed in normal parathyroid glands. In particular, they showed significant rhythmicity of parathyroid FGFR1, MafB and Gata3 transcription factors. Importantly, in CKD rats, there was deregulation of the parathyroid circadian clock genes and the cell cycle regulators Cyclin D1, c-Myc, Wee1 and p27, which are all influenced by the circadian clock [150]. Thus, a circadian clock operates in the parathyroid and its downstream cell cycle regulators are altered in CKD. The parathyroid circadian clock may contribute to parathyroid cell proliferation in SHP.

4. Summary

SHP is a progressive disease occurring in most CKD patients, with severe consequences for patient health. If poorly controlled, SHP progresses and leads to bone disease and soft tissue calcification, which influence morbidity and mortality. SHP is characterized by increased PTH secretion, gene expression and parathyroid cell proliferation. Studies in experimental SHP show that the high PTH gene expression in SHP is determined by post-transcriptional mechanisms mediated by protein binding to the PTH mRNA 3′-UTR. Pin1 coordinates these interactions. Decreased parathyroid Pin1 enzymatic activity in SHP alters the PTH mRNA–protein interaction, leading to increased PTH mRNA stability and levels. miRNAs provide an additional layer of post-transcriptional regulation of gene expression. Parathyroid-specific deletion of the miRNA maturating enzyme Dicer in PT-Dicer−/− mice results in a muted increase in PTH expression by both hypocalcemia and uremia, indicating that parathyroid miRNAs are crucial for the stimulation of the parathyroid in SHP. Profiling of the human, mouse and rat parathyroid miRNome by small-RNA sequencing showed that human and rodent parathyroids share similar miRNA profiles. SHP leads to the dysregulation of some of these, as well as other miRNAs. The evolutionary conservation of abundant miRNAs in normal parathyroids and the regulation of miRNA expression in SHP indicate their significance in parathyroid function and in the development of hyperparathyroidism. In addition to the stimulated PTH production per cell, increased parathyroid cell proliferation also contributes to SHP. The physiologic regulation of parathyroid cell hyperplasia by calcium, phosphate, 1,25D and FGF23 is interrupted in advanced CKD and SHP. Activation of pro-proliferative signaling pathways, such as the mTOR pathway, together with interruption of cell division gatekeepers, such as p21, lead to hyperplastic parathyroid glands in CKD. Disruption of the parathyroid circadian clock may also contribute to parathyroid cell proliferation in SHP. Figure 3 summarizes the complex mechanisms that contribute to the increased PTH production and parathyroid cell proliferation in CKD-induced SHP. In the lack of a functional parathyroid cell line, most studies were performed in experimental animal models that are supported by studies using human tissues. Understanding the molecular mechanisms of CKD-induced SHP may identify new intervention targets for the control of SHP.

Funding

The research was funded by grants from the Israel Science Foundation (Tally Naveh-Many, ISF 642/16; Morris Nechama, ISF 2030/21) and the US-Israel Binational Science Foundation (Tally Naveh-Many, BSF 2019300). Tally Naveh-Many, Oded Volovelsky and Morris Nechama are research associates of the Wohl Institute for Translation Research at the Hadassah-Hebrew University Medical Center.

Conflicts of Interest

The authors declare that they have no conflict of interest.

Abbreviations

PTHparathyroid hormone
SHPsecondary hyperparathyroidism
CKDchronic kidney disease
CaSRCalcium sensing receptor
VDRvitamin D receptor
FGF23fibroblast growth factor 23
MiRNAmicro-RNA
MiRNomemiRNA transcriptome
3′-UTR3′-untranslated region
AREAU-rich element
AUF1adenosine-uridine (AU)-rich binding factor 1
KSRPK-homology splicing regulatory protein
CPEB proteincytoplasmic polyadenylation element binding protein
PT-Dicer−/−parathyroid-specific gene deletion of Dicer
EGFRepidermal growth factor receptor
Mtormammalian target of rapamycin
mTORCmammalian target of rapamycin complex
TGF-αtransforming growth factor α
1:25D1,25 dihydroxy-vitamin D
NF-kBnuclear factor kappa B
COXCyclooxygenase
PGE2prostaglandin E2
EP2PGE2 receptor 2 subtype
FGFRfibroblast growth factor receptor
rpS6p−/−ribosomal protein S6 (rpS6) harboring alanine substitutions at all serine phosphorylation sites
MAPKmitogen-activated protein kinase
PRAD1parathyroid adenomatosis 1
MEN1multiple endocrine neoplasia type 1
AKTprotein kinase B

References

  1. Hannan, M.F.; Kallay, E.; Chang, W.; Brandi, M.L.; Thakker, R.V. The calcium-sensing receptor in physiology and in calcitropic and noncalcitropic diseases. Nat. Rev. Endocrinol. 2019, 15, 33–51. [Google Scholar] [CrossRef]
  2. Silver, J.; Levi, R. Regulation of pth synthesis and secretion relevant to the management of secondary hyperparathyroidism in chronic kidney disease. Kidney Int. Suppl. 2005, 67, S8–S12. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/15882315 (accessed on 20 December 2021). [CrossRef] [Green Version]
  3. Kumar, R.; Thompson, J.R. The regulation of parathyroid hormone secretion and synthesis. J. Am. Soc. Nephrol. 2011, 22, 216–224. Available online: https://pubmed.ncbi.nlm.nih.gov/21164021 (accessed on 20 December 2021). [CrossRef] [Green Version]
  4. Hofer, M.A.; Brown, E.M. Extracellular calcium sensing and signalling. Nat. Rev. Mol. Cell Biol. 2003, 4, 530–538. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/12838336 (accessed on 20 December 2021). [CrossRef]
  5. Brown, E.M.; MacLeod, R.J. Extracellular calcium sensing and extracellular calcium signaling. Physiol. Rev. 2001, 81, 239–297. [Google Scholar] [CrossRef]
  6. Drüeke, T.B. Modulation and action of the calcium-sensing receptor. Nephrol. Dial. Transplant. 2004, 19, v20–v26. [Google Scholar] [CrossRef] [Green Version]
  7. Slatopolsky, E.; Caglar, S.; Pennell, J.P.; Taggart, D.D.; Canterbury, J.M.; Reiss, E.; Bricker, N.S. On the pathogenesis of hyperparathyroidism in chronic experimental renal insufficiency in the dog. J. Clin. Investig. 1971, 50, 492–499. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/5545116 (accessed on 20 December 2021). [CrossRef] [Green Version]
  8. Kilav, R.; Silver, J.; Naveh-Many, T. Parathyroid hormone gene expression in hypophosphatemic rats. J. Clin. Investig. 1995, 96, 327–333. [Google Scholar] [CrossRef]
  9. Ben Dov, I.Z.; Galitzer, H.; Lavi-Moshayoff, V.; Goetz, R.; Kuro-o, M.; Mohammadi, M.; Sirkis, R.; Naveh-Many, T.; Silver, J. The parathyroid is a target organ for fgf23 in rats. J. Clin. Investig. 2007, 117, 4003–4008. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/17992255 (accessed on 20 December 2021). [CrossRef] [Green Version]
  10. Naveh-Many, T.; Silver, J. The pas de trois of vitamin d, fgf23, and pth. J. Am. Soc. Nephrol. 2016, 28, 393–395. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/27807212 (accessed on 20 December 2021). [CrossRef]
  11. Centeno, P.P.; Herberger, A.; Mun, H.-C.; Tu, C.; Nemeth, E.F.; Chang, W.; Conigrave, A.D.; Ward, D.T. Phosphate acts directly on the calcium-sensing receptor to stimulate parathyroid hormone secretion. Nat. Commun. 2019, 10, 4693. [Google Scholar] [CrossRef]
  12. Silver, J.; Naveh-Many, T.; Mayer, H.; Schmelzer, H.J.; Popovtzer, M.M. Regulation by vitamin d metabolites of parathyroid hormone gene transcription in vivo in the rat. J. Clin. Investig. 1986, 78, 1296–1301. [Google Scholar] [CrossRef] [Green Version]
  13. Silver, J.; Marks, R.; Naveh-Many, T. Regulation of parathyroid hormone and calcitonin gene expression by l,25-dihydroxyvitamin d3 and calcium. In Calcium Regulation and Bone Metabolism: Basic and Clinical Aspects; Cohn, D.V., Glorieux, F.H., Martin, T.J., Eds.; Excerpta Medica: Amsterdam, The Netherlands, 1990; pp. 140–145. [Google Scholar]
  14. Pike, J.W.; Meyer, M.B.; Watanuki, M.; Kim, S.; Zella, L.A.; Fretz, J.A.; Yamazaki, M.; Shev, N.K. Perspectives on mechanisms of gene regulation by 1,25-dihydroxyvitamin d3 and its receptor. J. Steroid Biochem. Mol. Biol. 2007, 103, 389–395. [Google Scholar] [CrossRef] [Green Version]
  15. Russell, J.; Ashok, S.; Koszewski, N.J. Vitamin d receptor interactions with the rat parathyroid hormone gene: Synergistic effects between two negative vitamin d response elements. J. Bone Miner. Res. 1999, 14, 1828–1837. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/0010571682 (accessed on 20 December 2021). [CrossRef]
  16. Krajisnik, T.; Bjorklund, P.; Marsell, R.; Ljunggren, O.; Akerstrom, G.; Jonsson, K.B.; Westin, G.; Larss, T.E.on. Fibroblast growth factor-23 regulates parathyroid hormone and 1alpha-hydroxylase expression in cultured bovine parathyroid cells. J. Endocrinol. 2007, 195, 125–131. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/17911404 (accessed on 20 December 2021). [CrossRef] [Green Version]
  17. Naveh-Many, T.; Rahamimov, R.; Livni, N.; Silver, J. Parathyroid cell proliferation in normal and chronic renal failure rats: The effects of calcium, phosphate and vitamin d. J. Clin. Investig. 1995, 96, 1786–1793. [Google Scholar] [CrossRef]
  18. Levi, R.; Ben Dov, I.Z.; Lavi-Moshayoff, V.; Dinur, M.; Martin, D.; Naveh-Many, T.; Silve, J. Increased parathyroid hormone gene expression in secondary hyperparathyroidism of experimental uremia is reversed by calcimimetics: Correlation with posttranslational modification of the trans acting factor auf1. J. Am. Soc. Nephrol. 2006, 17, 107–112. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/16291838 (accessed on 20 December 2021). [CrossRef] [Green Version]
  19. Goodman, W.G.; Quarles, L.D. Development and progression of secondary hyperparathyroidism in chronic kidney disease: Lessons from molecular genetics. Kidney Int. 2008, 74, 276–288. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/17568787 (accessed on 20 December 2021). [CrossRef] [Green Version]
  20. Lewin, E.; Huan, J.; Olgaard, K. Parathyroid growth and suppression in renal failure. Semin. Dial. 2006, 19, 238–245. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/16689976 (accessed on 20 December 2021). [CrossRef]
  21. Brown, A.J.; Dusso, A.; Lopez-Hilker, S.; Lewis-Finch, J.; Grooms, P.; Slatopolsky, E. 1,25-(oh)2d receptors are decreased in parathyroid glands from chronically uremic dogs. Kidney Int. 1989, 35, 19–23. [Google Scholar] [CrossRef] [Green Version]
  22. Silver, J.; Kilav, R.; Naveh-Many, T. Mechanisms of secondary hyperparathyroidism. Am. J. Physiol. Ren. Physiol. 2002, 283, F367–F376. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/12167586 (accessed on 20 December 2021). [CrossRef] [Green Version]
  23. Moallem, E.; Silver, J.; Kilav, R.; Naveh-Many, T. Rna protein binding and post-transcriptional regulation of pth gene expression by calcium and phosphate. J. Biol. Chem. 1998, 273, 5253–5259. [Google Scholar] [CrossRef] [Green Version]
  24. Sela-Brown, A.; Silver, J.; Brewer, G.; Naveh-Many, T. Identification of auf1 as a parathyroid hormone mrna 3′-untranslated region binding protein that determines parathyroid hormone mrna stability. J. Biol. Chem. 2000, 275, 7424–7429. [Google Scholar] [CrossRef] [Green Version]
  25. Nechama, M.; Ben Dov, I.Z.; Briata, P.; Gherzi, R.; Naveh-Many, T. The mrna decay promoting factor k-homology splicing regulator protein post-transcriptionally determines parathyroid hormone mrna levels. FASEB J. 2008, 22, 3458–3468. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/18583400 (accessed on 20 December 2021). [CrossRef]
  26. Kilav-Levin, R.; Hassan, A.; Nechama, M.; Shilo, V.; Silver, J.; Ben-Dov, I.Z.; Naveh-Many, T. Post-transcriptional mechanisms regulating parathyroid hormone gene expression in secondary hyperparathyroidism. FEBS J. 2020, 287, 2903–2913. [Google Scholar] [CrossRef] [Green Version]
  27. Wilson, G.M.; Brewer, G. The search for trans-acting factors controlling messenger rna decay. Prog. Nucleic Acid Res. Mol. Biol. 1999, 62, 257–291. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/0009932457 (accessed on 20 December 2021).
  28. Briata, P.; Chen, C.Y.; Giovarelli, M.; Pasero, M.; Trabucchi, M.; Ramos, A.; Gherzi, R. Ksrp, many functions for a single protein. Front. Biosci. (Landmark Ed.) 2011, 16, 1787–1796. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/21196264 (accessed on 20 December 2021). [CrossRef]
  29. Barreau, C.; Paillard, L.; Osborne, H.B. Au-rich elements and associated factors: Are there unifying principles? Nucleic Acids Res. 2006, 33, 7138–7150. [Google Scholar] [CrossRef]
  30. Garneau, N.L.; Wilusz, J.; Wilusz, C.J. The highways and byways of mrna decay. Nat. Rev. Mol. Cell Biol. 2007, 8, 113–126. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/17245413 (accessed on 20 December 2021). [CrossRef]
  31. Peng, S.S.; Chen, C.Y.; Xu, N.; Shyu, A.B. Rna stabilization by the au-rich element binding protein, hur, an elav protein. EMBO J. 1998, 17, 3461–3470. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/9628881 (accessed on 20 December 2021). [CrossRef]
  32. Wickens, M.; Anderson, P.; Jakson, R.J. Life and death in the cytoplasm: Messages from the 3’ end. Curr. Opin. Genet. Dev. 1996, 7, 220–232. [Google Scholar] [CrossRef]
  33. Chen, C.Y.; Shyu, A.B. Au-rich elements: Characterization and importance in mrna degradation. Trends Biochem. Sci. 1995, 20, 465–470. Available online: http://www.ncbi.nlm.nih.gov/pubmed/8578590 (accessed on 20 December 2021). [CrossRef]
  34. Zhang, W.; Wagner, B.J.; Ehrenman, K.; Schaefer, A.W.; DeMaria, C.T.; Crater, D.; DeHaven, K.; Long, L.; Brewer, G. Purification, characterization, and cdna cloning of an au-rich element rna-binding protein, auf1. Mol. Cell Biol. 1993, 13, 7652–7665. [Google Scholar]
  35. Gherzi, R.; Trabucchi, M.; Ponassi, M.; Ruggiero, T.; Corte, G.; Moroni, C.; Chen, C.Y.; Khabar, K.S.; Andersen, J.S.; Briata, P. The rna-binding protein ksrp promotes decay of beta-catenin mrna and is inactivated by pi3k-akt signaling. PLoS Biol. 2006, 5, e5. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/17177604 (accessed on 20 December 2021). [CrossRef]
  36. DeMaria, C.T.; Brewer, G. Auf1 binding affinity to a+u-rich elements correlates with rapid mrna degradation. J. Biol. Chem. 1996, 271, 12179–12184. [Google Scholar] [CrossRef] [Green Version]
  37. Kiledjian, M.; DeMaria, C.T.; Brewer, G.; Novick, K. Identification of auf1 (heterogeneous nclear ribonucleoprotein d) as a component of the a-globin mrna stability complex. Mol. Cell Biol. 1997, 17, 4870–4876. [Google Scholar] [CrossRef] [Green Version]
  38. Gherzi, R.; Lee, K.Y.; Briata, P.; Wegmuller, D.; Moroni, C.; Karin, M.; Chen, C.Y. A kh domain rna binding protein, ksrp, promotes are-directed mrna turnover by recruiting the degradation machinery. Mol. Cell 2004, 14, 571–583. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/15175153 (accessed on 20 December 2021). [CrossRef]
  39. Esnault, S.; Shen, Z.J.; Whitesel, E.; Malter, J.S. The peptidyl-prolyl isomerase pin1 regulates granulocyte-macrophage colony-stimulating factor mrna stability in t lymphocytes. J. Immunol. 2006, 177, 6999–7006. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/17082615 (accessed on 20 December 2021). [CrossRef] [PubMed]
  40. Bell, O.; Gaberman, E.; Kilav, R.; Levi, R.; Cox, K.B.; Molkentin, J.D.; Silver, J.; Naveh-Many, T. The protein phosphatase calcineurin determines basal parathyroid hormone gene expression. Mol. Endocrinol. 2005, 19, 516–526. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  41. Di¡az-Moreno, I.; Hollingworth, D.; Frenkiel, T.A.; Kelly, G.; Martin, S.; Howell, S.; García-Mayoral, M.A.; Gherzi, R.; Briata, P.; Ramos, A. Phosphorylation-mediated unfolding of a kh domain regulates ksrp localization via 14-3-3 binding. Nat. Struct. Mol. Biol. 2009, 16, 238–246. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pmc/articles/PMC2858377/ (accessed on 20 December 2021). [CrossRef] [PubMed] [Green Version]
  42. Briata, P.; Forcales, S.V.; Ponassi, M.; Corte, G.; Chen, C.Y.; Karin, M.; Puri, P.L.; Gherzi, R. P38-dependent phosphorylation of the mrna decay-promoting factor ksrp controls the stability of select myogenic transcripts. Mol. Cell. 2005, 20, 891–903. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/16364914 (accessed on 20 December 2021). [CrossRef] [PubMed]
  43. Wilson, G.M.; Lu, J.; Sutphen, K.; Suarez, Y.; Sinha, S.; Brewer, B.; Villanueva-Feliciano, E.C.; Ysla, R.M.; Charles, S.; Brewe, G. Phosphorylation of p40auf1 regulates binding to a + u-rich mrna-destabilizing elements and protein-induced changes in ribonucleoprotein structure. J. Biol. Chem. 2003, 278, 33039–33048. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/12819194 (accessed on 20 December 2021). [CrossRef] [PubMed] [Green Version]
  44. Lee, E.K.; Gorospe, M. Minireview: Posttranscriptional regulation of the insulin and insulin-like growth factor systems. Endocrinology 2010, 151, 1403–1408. Available online: https://pubmed.ncbi.nlm.nih.gov/20032049 (accessed on 20 December 2021). [CrossRef] [PubMed] [Green Version]
  45. Ing, N.H. Steroid hormones regulate gene expression posttranscriptionally by altering the stabilities of messenger rnas. Biol. Reprod. 2005, 72, 1290–1296. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Nair, A.K.; Kash, J.C.; Peegel, H.; Meno, K.M.J. Post-transcriptional regulation of luteinizing hormone receptor mrna in the ovary by a novel mrna-binding protein. J. Biol. Chem. 2002, 277, 21468–21473. Available online: http://www.jbc.org/content/277/24/21468.abstract (accessed on 20 December 2021). [CrossRef] [Green Version]
  47. Menon, K.M.J.; Menon, B.; Gulappa, T. Regulation of luteinizing hormone receptor mrna expression in the ovary: The role of mir-122. Vitam. Horm. 2018, 107, 67–87. Available online: https://pubmed.ncbi.nlm.nih.gov/29544643 (accessed on 20 December 2021). [CrossRef]
  48. Shilo, V.; Silver, J.; Naveh-Many, T. Micro-rnas in the parathyroid: A new portal in understanding secondary hyperparathyroidism. Curr. Opin. Nephrol. Hypertens. 2016, 25, 271–277. [Google Scholar] [CrossRef]
  49. Kilav, R.; Silver, J.; Naveh-Man, T. A conserved cis-acting element in the parathyroid hormone 3′-untranslated region is sufficient for regulation of rna stability by calcium and phosphate. J. Biol. Chem. 2001, 276, 8727–8733. [Google Scholar] [CrossRef] [Green Version]
  50. Lu, K.P.; Zhou, X.Z. The prolyl isomerase pin1: A pivotal new twist in phosphorylation signalling and disease. Nat. Rev. Mol. Cell Biol. 2007, 8, 904–916. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/17878917 (accessed on 20 December 2021). [CrossRef]
  51. Lu, K.P.; Hanes, S.D.; Hunter, T. A human peptidyl-prolyl isomerase essential for regulation of mitosis. Nature 1996, 380, 544–547. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/8606777 (accessed on 20 December 2021).
  52. Thapar, R. Roles of prolyl isomerases in rna-mediated gene expression. Biomolecules 2015, 5, 974–999. Available online: https://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/25992900 (accessed on 20 December 2021). [CrossRef] [PubMed]
  53. Shen, Z.J.; Malter, J.S. Regulation of au-rich element rna binding proteins by phosphorylation and the prolyl isomerase pin1. Biomolecules 2015, 5, 412–434. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  54. Nechama, M.; Uchida, T.; Yosef-Levi, I.M.; Silver, J.; Naveh-Many, T. The peptidyl-prolyl isomerase pin1 determines parathyroid hormone mrna levels and stability in rat models of secondary hyperparathyroidism. J. Clin. Investig. 2009, 119, 3102–3114. [Google Scholar] [CrossRef] [PubMed]
  55. Shen, Z.J.; Esnault, S.; Rosenthal, L.A.; Szakaly, R.J.; Sorkness, R.L.; Westmark, P.R.; Sandor, M.; Malter, J.S. Pin1 regulates tgf-beta1 production by activated human and murine eosinophils and contributes to allergic lung fibrosis. J. Clin. Investig. 2008, 118, 479–490. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/18188456 (accessed on 20 December 2021).
  56. Shen, Z.J.; Esnault, S.; Malter, J.S. The peptidyl-prolyl isomerase pin1 regulates the stability of granulocyte-macrophage colony-stimulating factor mrna in activated eosinophils. Nat. Immunol. 2005, 6, 1280–1287. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/16273101 (accessed on 20 December 2021). [CrossRef]
  57. Nechama, M.; Lin, C.L.; Richter, J.D. An unusual two-step control of cpeb destruction by pin1. Mol. Cell Biol. 2013, 33, 48–58. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/23090969 (accessed on 20 December 2021). [CrossRef] [Green Version]
  58. Schelhorn, C.; Martín-Malpartida, P.; Suñol, D.; Macias, M.J. Structural analysis of the pin1-cpeb1 interaction and its potential role in cpeb1 degradation. Sci. Rep. 2015, 5, 14990. Available online: https://0-www-nature-com.brum.beds.ac.uk/articles/srep14990#supplementary-information (accessed on 20 December 2021). [CrossRef] [Green Version]
  59. Kumar, R. Pin1 regulates parathyroid hormone mrna stability. J. Clin. Investig. 2009, 119, 2887–2891. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/19770518 (accessed on 20 December 2021). [CrossRef] [Green Version]
  60. Oster, M.; Reyer, H.; Gerlinger, C.; Trakooljul, N.; Siengdee, P.; Keiler, J.; Ponsuksili, S.; Wolf, P.; Wimme, K. Mrna profiles of porcine parathyroid glands following variable phosphorus supplies throughout fetal and postnatal life. Biomedicines 2021, 9, 454. Available online: https://pubmed.ncbi.nlm.nih.gov/33922173 (accessed on 20 December 2021). [CrossRef]
  61. Santamaria, I.; Alvarez-Hernandez, D.; Jofre, R.; Polo, J.R.; Menarguez, J.; Cannata-Andi, J.B. Progression of secondary hyperparathyroidism involves deregulation of genes related to DNA and rna stability. Kidney Int. 2005, 67, 2267–2279. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/15882268 (accessed on 20 December 2021). [CrossRef] [Green Version]
  62. Balenga, N.; Azimzadeh, P.; Hogue, J.A.; Staats, P.N.; Shi, Y.; Koh, J.; Dressman, H.; Olson, J.A. Orphan adhesion gpcr gpr64/adgrg2 is overexpressed in parathyroid tumors and attenuates calcium-sensing receptor-mediated signaling. J. Bone Miner. Res. 2017, 32, 654–666. [Google Scholar] [CrossRef] [PubMed]
  63. Zhao, Y.; Zhang, L.-L.; Ding, F.-X.; Cao, P.; Qi, Y.-Y.; Wan, J. Pin1 and secondary hyperparathyroidism of chronic kidney disease: Gene polymorphisms and protein levels. Ren. Fail. 2017, 39, 159–165. [Google Scholar] [CrossRef] [PubMed]
  64. Bartel, D.P. Micrornas: Target recognition and regulatory functions. Cell 2009, 136, 215–233. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/19167326 (accessed on 20 December 2021). [CrossRef] [PubMed] [Green Version]
  65. Hafner, M.; Landgraf, P.; Ludwig, J.; Rice, A.; Ojo, T.; Lin, C.; Holoch, D.; Lim, C.; Tuschl, T. Identification of micrornas and other small regulatory rnas using cdna library sequencing. Methods 2008, 44, 3–12. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/18158127 (accessed on 20 December 2021). [CrossRef] [PubMed] [Green Version]
  66. Lee, Y.; Ahn, C.; Han, J.J.; Choi, H.; Kim, J.; Yim, J.; Lee, J.; Provost, P.; Radmark, O.; Kim, S.; et al. The nuclear rnase iii drosha initiates microrna processing. Nature 2003, 425, 415–419. [Google Scholar] [CrossRef] [PubMed]
  67. Bernstein, E.; Kim, S.Y.; Carmell, M.A.; Murchison, E.P.; Alcorn, H.; Li, M.Z.; Mills, A.A.; Elledge, S.J.; Anderson, K.V.; Hannon, G.J. Dicer is essential for mouse development. Nat. Genet. 2003, 35, 215–217. [Google Scholar] [CrossRef]
  68. Chen, J.F.; Murchison, E.P.; Tang, R.; Callis, T.E.; Tatsuguchi, M.; Deng, Z.; Rojas, M.; Hammond, S.M.; Schneider, M.D.; Selzman, C.H.; et al. Targeted deletion of dicer in the heart leads to dilated cardiomyopathy and heart failure. Proc. Natl. Acad. Sci. USA 2008, 105, 2111–2116. [Google Scholar] [CrossRef] [Green Version]
  69. Melkman-Zehavi, T.; Oren, R.; Kredo-Russo, S.; Shapira, T.; Mandelbaum, A.D.; Rivkin, N.; Nir, T.; Lennox, K.A.; Behlke, M.A.; Dor, Y.; et al. Mirnas control insulin content in pancreatic beta-cells via downregulation of transcriptional repressors. EMBO J. 2011, 30, 835–845. [Google Scholar] [CrossRef] [Green Version]
  70. Harfe, B.D.; McManus, M.T.; Mansfield, J.H.; Hornstein, E.; Tabin, C.J. The rnaseiii enzyme dicer is required for morphogenesis but not patterning of the vertebrate limb. Proc. Natl. Acad. Sci. USA 2005, 102, 10898–10903. [Google Scholar] [CrossRef] [Green Version]
  71. Shilo, V.; Dov, I.Z.B.; Nechama, M.; Silver, J.; Naveh-Many, T. Parathyroid-specific deletion of dicer-dependent micrornas abrogates the response of the parathyroid to acute and chronic hypocalcemia and uremia. FASEB J. 2015, 29, 3964–3976. [Google Scholar] [CrossRef] [Green Version]
  72. Aurilia, C.; Donati, S.; Palmini, G.; Miglietta, F.; Falsetti, I.; Iantomasi, T.; Brandi, M.L. Are non-coding rnas useful biomarkers in parathyroid tumorigenesis? Int. J. Mol. Sci. 2021, 22, 10465. [Google Scholar] [CrossRef] [PubMed]
  73. Verdelli, C.; Forno, I.; Vaira, V.; Corbetta, S. Epigenetic alterations in human parathyroid tumors. Endocrine 2015, 49, 324–332. [Google Scholar] [CrossRef] [PubMed]
  74. Guarnieri, V.; Muscarella, L.A.; Verdelli, C.; Corbetta, S. Alterations of DNA methylation in parathyroid tumors. Mol. Cell Endocrinol. 2018, 469, 60–69. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/28501573 (accessed on 20 December 2021). [CrossRef] [PubMed]
  75. Verdelli, C.; Corbetta, S. Epigenetic alterations in parathyroid cancers. Int. J. Mol. Sci. 2017, 18, 310. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/28157158 (accessed on 20 December 2021). [CrossRef] [PubMed] [Green Version]
  76. Silva-Figueroa, A.M.; Perrier, N.D. Epigenetic processes in sporadic parathyroid neoplasms. Mol. Cell Endocrinol. 2018, 469, 54–59. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/28400272 (accessed on 20 December 2021). [CrossRef] [PubMed]
  77. Mizamtsidi, M.; Nastos, K.; Palazzo, F.; Constantinides, V.; Dina, R.; Farenden, M.; Mastorakos, G.; Vassiliou, I.; Gazouli, M. Association between hsa-mir-30e polymorphisms and sporadic primary hyperparathyroidism risk. In Vivo 2019, 33, 1263–1269. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/31280217 (accessed on 20 December 2021). [CrossRef] [Green Version]
  78. Mizamtsidi, M.; Nastos, C.; Mastorakos, G.; Dina, R.; Vassiliou, I.; Gazouli, M.; Palazzo, F. Diagnosis, management, histology and genetics of sporadic primary hyperparathyroidism: Old knowledge with new tricks. Endocr. Connect. 2018, 7, R56–R68. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/29330338 (accessed on 20 December 2021). [CrossRef] [Green Version]
  79. Vaira, V.; Elli, F.; Forno, I.; Guarnieri, V.; Verdelli, C.; Ferrero, S.; Scillitani, A.; Vicentini, L.; Cetani, F.; Mantovani, G.; et al. The microrna cluster c19mc is deregulated in parathyroid tumours. J. Mol. Endocrinol. 2012, 49, 115–124. [Google Scholar] [CrossRef] [Green Version]
  80. Corbetta, S.; Vaira, V.; Guarnieri, V.; Scillitani, A.; Eller-Vainicher, C.; Ferrero, S.; Vicentini, L.; Chiodini, I.; Bisceglia, M.; Beck-Peccoz, P.; et al. Differential expression of micrornas in human parathyroid carcinomas compared with normal parathyroid tissue. Endocr. Relat. Cancer 2010, 17, 135–146. [Google Scholar] [CrossRef] [Green Version]
  81. Shilo, V.; Levi, I.M.; Abel, R.; Mihailović, A.; Wasserman, G.; Naveh-Many, T.; Ben-Dov, I.Z. Let-7 and microrna-148 regulate parathyroid hormone levels in secondary hyperparathyroidism. J. Am. Soc. Nephrol. 2017, 28, 2353–2363. Available online: http://jasn.asnjournals.org/content/early/2017/03/14/ASN.2016050585.abstract (accessed on 20 December 2021). [CrossRef] [Green Version]
  82. Esau, C.C. Inhibition of microrna with antisense oligonucleotides. Methods 2008, 44, 55–60. [Google Scholar] [CrossRef] [PubMed]
  83. Wang, Q.; Palnitkar, S.; Parfitt, A.M. Parathyroid cell proliferation in the rat: Effect of age and of phosphate administration and recovery. Endocrinology 1996, 137, 4558–4562. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  84. Parfitt, A.M. Parathyroid growth, normal and abnormal. In The Parathyroids; Bilezikian, J.P., Levine, M.A., Marcus, R., Eds.; Raven Press, Ltd.: New York, NY, USA, 1994; pp. 373–405. [Google Scholar]
  85. Tominaga, Y.; Kohara, S.; Namii, Y.; Nagasaka, T.; Haba, T.; Uchida, K.; Numano, M.; Tanaka, Y.; Takagi, H. Clonal analysis of nodular parathyroid hyperplasia in renal hyperparathyroidism. World J. Surg. 1996, 20, 744–750, discussion 50–52. [Google Scholar] [CrossRef] [PubMed]
  86. Arnold, A.; Brown, M.F.; Urena, P.; Gaz, R.D.; Sarfati, E.; Drueke, T.B. Monoclonality of parathyroid tumors in chronic renal failure and in primary parathyroid hyperplasia. J. Clin. Investig. 1995, 95, 2047–2053. [Google Scholar] [CrossRef]
  87. Drueke, T.B. Cell biology of parathyroid gland hyperplasia in chronic renal failure. J. Am. Soc. Nephrol. 2000, 11, 1141–1152. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/0010820180 (accessed on 20 December 2021). [CrossRef]
  88. Denda, M.; Finch, J.; Slatopolsky, E. Phosphorus accelerates the development of parathyroid hyperplasia and secondary hyperparathyroidism in rats with renal failure. Am. J. Kidney Dis. 1996, 28, 596–602. [Google Scholar] [CrossRef]
  89. Yokozawa, T.; Zheng, P.D.; Oura, H.; Koizumi, F. Animal model of adenine-induced chronic renal failure in rats. Nephron 1986, 44, 230–234. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/3785486 (accessed on 20 December 2021). [CrossRef]
  90. Ceballos-Picot, I.; Saha, A.; Arora, N.; Kapoor, K.; Kaur, M.; Dhull, R.S.; Goyal, S. Adenine phosphoribosyltransferase deficiency due to novel mutation. Kidney Int. Rep. 2018, 4, 624–628. Available online: https://pubmed.ncbi.nlm.nih.gov/30993240 (accessed on 20 December 2021). [CrossRef] [Green Version]
  91. Jia, T.; Olauson, H.; Lindberg, K.; Amin, R.; Edvardsson, K.; Lindholm, B.; Andersson, G.; Wernerson, A.; Sabbagh, Y.; Schiavi, S.; et al. A novel model of adenine-induced tubulointerstitial nephropathy in mice. BMC Nephrol. 2013, 14, 116. [Google Scholar] [CrossRef] [Green Version]
  92. Ritter, C.S.; Finch, J.L.; Slatopolsky, E.A.; Brown, A.J. Parathyroid hyperplasia in uremic rats precedes down-regulation of the calcium receptor. Kidney Int. 2001, 60, 1737–1744. [Google Scholar] [CrossRef] [Green Version]
  93. Galitzer, H.; Dov, I.Z.B.; Silver, J.; Naveh-Many, T. Parathyroid cell resistance to fibroblast growth factor 23 in secondary hyperparathyroidism of chronic kidney disease. Kidney Int. 2010, 77, 211–218. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/20016468 (accessed on 20 December 2021). [CrossRef] [PubMed] [Green Version]
  94. Komaba, H.; Goto, S.; Fujii, H.; Hamada, Y.; Kobayashi, A.; Shibuya, K.; Tominaga, Y.; Otsuki, N.; Nibu, K.I.; Nakagawa, K.; et al. Depressed expression of klotho and fgf receptor 1 in hyperplastic parathyroid glands from uremic patients. Kidney Int. 2010, 77, 232–238. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/19890272 (accessed on 20 December 2021). [CrossRef] [PubMed] [Green Version]
  95. Canalejo, R.; Canalejo, A.; Martinez-Moreno, J.M.; Rodriguez-Ortiz, M.E.; Estepa, J.C.; Mendoza, F.J.; Munoz-Castaneda, J.R.; Shalhoub, V.; Almaden, Y.; Rodriguez, M. Fgf23 fails to inhibit uremic parathyroid glands. J. Am. Soc. Nephrol. 2010, 21, 1125–1135. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  96. Lewin, E.; Garfia, B.; Recio, F.L.; Rodriguez, M.; Olgaard, K. Persistent downregulation of calcium-sensing receptor mrna in rat parathyroids when severe secondary hyperparathyroidism is reversed by an isogenic kidney transplantation. J. Am. Soc. Nephrol. 2002, 13, 2110–2116. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/12138143 (accessed on 20 December 2021). [CrossRef] [PubMed] [Green Version]
  97. Garfia, B.; Canadillas, S.; Canalejo, A.; Luque, F.; Siendones, E.; Quesada, M.; Almaden, Y.; Aguilera-Tejero, E.; Rodriguez, M. Regulation of parathyroid vitamin d receptor expression by extracellular calcium. J. Am. Soc. Nephrol. 2002, 13, 2945–2952. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/12444213 (accessed on 20 December 2021). [CrossRef] [Green Version]
  98. Healy, K.D.; Vanhooke, J.L.; Prahl, J.M.; DeLuca, H.F. Parathyroid hormone decreases renal vitamin d receptor expression in vivo. Proc. Natl. Acad. Sci. USA 2005, 102, 4724–4728. Available online: https://pubmed.ncbi.nlm.nih.gov/15769857 (accessed on 20 December 2021). [CrossRef] [Green Version]
  99. Naveh-Many, T.; Volovelsky, O. Parathyroid cell proliferation in secondary hyperparathyroidism of chronic kidney disease. Int. J. Mol. Sci. 2020, 21, 4332. Available online: https://0-www-mdpi-com.brum.beds.ac.uk/1422-0067/21/12/4332 (accessed on 20 December 2021). [CrossRef]
  100. Rodríguez, M.; Goodman, W.G.; Liakopoulos, V.; Messa, P.; Wiecek, A.; Cunningham, J. The use of calcimimetics for the treatment of secondary hyperparathyroidism: A 10 year evidence review. Semin. Dial. 2015, 28, 497–507. [Google Scholar] [CrossRef]
  101. Canaff, L.; Hendy, G.N. Human calcium-sensing receptor gene. Vitamin d response elements in promoters p1 and p2 confer transcriptional responsiveness to 1,25-dihydroxyvitamin d. J. Biol. Chem. 2002, 277, 30337–30350. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/12036954 (accessed on 20 December 2021). [CrossRef] [Green Version]
  102. Denda, M.; Finch, J.; Brown, A.J.; Nishii, Y.; Kubodera, N.; Slatopolsky, E. 1,25-dihydroxyvitamin d3 and 22-oxacalcitriol prevent the decrease in vitamin d receptor content in the parathyroid glands of uremic rats. Kidney Int. 1996, 50, 34–39. [Google Scholar] [CrossRef] [Green Version]
  103. Sakai, M.; Tokunaga, S.; Kawai, M.; Murai, M.; Kobayashi, M.; Kitayama, T.; Saeki, S.; Kawata, T. Evocalcet prevents ectopic calcification and parathyroid hyperplasia in rats with secondary hyperparathyroidism. PLoS ONE 2020, 15, e0232428. Available online: https://pubmed.ncbi.nlm.nih.gov/32343734 (accessed on 20 December 2021). [CrossRef] [PubMed]
  104. Meola, M.; Petrucci, I.; Barsotti, G. Long-term treatment with cinacalcet and conventional therapy reduces parathyroid hyperplasia in severe secondary hyperparathyroidism. Nephrol. Dial. Transplant. 2009, 24, 982–989. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  105. Mendoza, F.J.; Lopez, I.; Canalejo, R.; Almaden, Y.; Martin, D.; Aguilera-Tejero, E.; Rodriguez, M. Direct upregulation of parathyroid calcium-sensing receptor and vitamin d receptor by calcimimetics in uremic rats. Am. J. Physiol. Ren. Physiol. 2009, 296, F605–F613. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  106. Nechama, M.; Dov, I.Z.B.; Silver, J.; Naveh-Many, T. Regulation of pth mrna stability by the calcimimetic r568 and the phosphorus binder lanthanum carbonate in ckd. Am. J. Physiol. Ren. Physiol. 2009, 296, F795–F800. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/19129257 (accessed on 20 December 2021). [CrossRef] [Green Version]
  107. Haven, C.J.; Howell, V.M.; Eilers, P.H.; Dunne, R.; Takahashi, M.; van Puijenbroek, M.; Furge, K.; Kievit, J.; Tan, M.H.; Fleuren, G.J.; et al. Gene expression of parathyroid tumors: Molecular subclassification and identification of the potential malignant phenotype. Cancer Res. 2004, 64, 7405–7411. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/15492263 (accessed on 20 December 2021). [CrossRef] [Green Version]
  108. Libutti, S.K.; Crabtree, J.S.; Lorang, D.; Burns, A.L.; Mazzanti, C.; Hewitt, S.M.; O’Connor, S.; Ward, J.M.; Emmert-Buck, M.R.; Remaley, A.; et al. Parathyroid gland-specific deletion of the mouse men1 gene results in parathyroid neoplasia and hypercalcemic hyperparathyroidism. Cancer Res. 2003, 63, 8022–8028. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/14633735 (accessed on 20 December 2021).
  109. Mulligan, L.M.; Marsh, D.J.; Robinson, B.G.; Schuffenecker, I.; Zedenius, J.; Lips, C.J.; Gagel, R.F.; Takai, S.I.; Noll, W.W.; Fink, M.; et al. Genotype-phenotype correlation in multiple endocrine neoplasia type 2: Report of the international ret mutation consortium. J. Intern. Med. 1995, 238, 343–346. [Google Scholar] [CrossRef]
  110. Hsi, E.D.; Zukerberg, L.R.; Yang, W.I.; Arnold, A. Cyclin d1/prad1 expression in parathyroid adenomas: An immunohistochemical study. J. Clin. Endocrinol. Metab. 1996, 81, 1736–1739. [Google Scholar]
  111. Motokura, T.; Arnold, A. Prad1/cyclin d1 proto-oncogene: Genomic organization, 5′ DNA sequence, and sequence of a tumor-specific rearrangement breakpoint. Genes Chromosom.Cancer 1993, 7, 89–95. [Google Scholar] [CrossRef]
  112. Arnold, A. Molecular basis of primary hyperparathyroidism. In The Parathyroids; Bilezikian, J.P., Levine, M.A., Marcus, R., Eds.; Raven Press, Ltd.: New York, NY, USA, 1994; pp. 407–421. [Google Scholar]
  113. Brewer, K.; Costa-Guda, J.; Arnold, A. Molecular genetic insights into sporadic primary hyperparathyroidism. Endocr. Relat. Cancer 2019, 26, R53–R72. [Google Scholar] [CrossRef]
  114. Imanishi, Y.; Hosokawa, Y.; Yoshimoto, K.; Schipani, E.; Mallya, S.; Papanikolaou, A.; Kifor, O.; Tokura, T.; Sablosky, M.; Ledgard, F.; et al. Primary hyperparathyroidism caused by parathyroid-targeted overexpression of cyclin d1 in transgenic mice. J. Clin. Investig. 2001, 107, 1093–1102. [Google Scholar] [CrossRef] [PubMed]
  115. Hirama, T.; Koeffler, H.P. Role of the cyclin-dependent kinase inhibitors in the development of cancer. Blood 1995, 86, 841–854. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  116. Tominaga, Y.; Tsuzuki, T.; Uchida, K.; Haba, T.; Otsuka, S.; Ichimori, T.; Yamada, K.; Numano, M.; Tanaka, Y.; Takagi, H. Expression of prad1/cyclin d1, retinoblastoma gene products, and ki67 in parathyroid hyperplasia caused by chronic renal failure versus primary adenoma. Kidney Int. 1999, 55, 1375–1383. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  117. Graña, X.; Reddy, E.P. Cell cycle control in mammalian cells: Role of cyclins, cyclin dependent kinases (cdks), growth suppressor genes and cyclin-dependent kinase inhibitors (ckis). Oncogene 1995, 11, 211–219. [Google Scholar]
  118. Dusso, A.; Pavlopoulos, T.; Naumovich, L.; Lu, Y.; Finch, J.; Brown, A.J.; Morrissey, J.; Slatopolsky, E. P21waf1 and transforming growth factor-alpha mediate dietary posphate regulation of parathyroid cell growth. Kidney Int. 2001, 59, 855–865. [Google Scholar] [CrossRef] [Green Version]
  119. Tokumoto, M.; Tsuruya, K.; Fukuda, K.; Kanai, H.; Kuroki, S.; Hirakata, H. Reduced p21, p27 and vitamin d receptor in the nodular hyperplasia in patients with advanced secondary hyperparathyroidism. Kidney Int. 2002, 62, 1196–1207. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/12234290 (accessed on 20 December 2021). [CrossRef]
  120. Cozzolino, M.; Lu, Y.; Finch, J.; Slatopolsky, E.; Dusso, A.S. P21waf1 and tgf-alpha mediate parathyroid growth arrest by vitamin d and high calcium. Kidney Int. 2001, 60, 2109–2117. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/11737585 (accessed on 20 December 2021). [CrossRef] [Green Version]
  121. Gogusev, J.; Duchambon, P.; Stoermann-Chopard, C.; Giovannini, M.; Sarfati, E.; Drueke, T.B. De novo expression of transforming growth factor-alpha in parathyroid gland tissue of patients with primary or secondary uraemic hyperparathyroidism. Nephrol. Dial. Transplant. 1996, 11, 2155–2162. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/8941573 (accessed on 20 December 2021). [CrossRef]
  122. Arcidiacono, M.V.; Sato, T.; Alvarez-Hernandez, D.; Yang, J.; Tokurl, M.; Gonzalez-Suarez, I.; Lu, Y.; Tominaga, Y.; Cannata-Andia, J.; Slatopolsky, E.; et al. Egfr activation increases parathyroid hyperplasia and calcitriol resistance in kidney disease. J. Am. Soc. Nephrol. 2008, 19, 310–320. [Google Scholar] [CrossRef] [Green Version]
  123. Cozzolino, M.; Lu, Y.; Sato, T.; Yang, J.; Suarez, I.G.; Brancaccio, D.; Slatopolsky, E.; Dusso, A.S. A critical role for enhanced tgf-alpha and egfr expression in the initiation of parathyroid hyperplasia in experimental kidney disease. Am. J. Physiol. Ren. Physiol. 2005, 289, F1096-102. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/15998841 (accessed on 20 December 2021). [CrossRef] [Green Version]
  124. Terada, Y.; Inoshita, S.; Nakashima, O.; Kuwahara, M.; Sasaki, S.; Marumo, F. Regulation of cyclin d1 expression and cell cycle progression by mitogen-activated protein kinase cascade. Kidney Int. 1999, 56, 1258–1261. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  125. Arcidiacono, M.V.; Yang, J.; Fernandez, E.; Dusso, A. Parathyroid-specific epidermal growth factor-receptor inactivation prevents uremia-induced parathyroid hyperplasia in mice. Nephrol. Dial. Transplant. 2015, 30, 434–440. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  126. Li, Z.; Yang, Z.; Passaniti, A.; Lapidus, R.G.; Liu, X.; Cullen, K.J.; Dan, H.C. A positive feedback loop involving egfr/akt/mtorc1 and ikk/nf-kb regulates head and neck squamous cell carcinoma proliferation. Oncotarget 2016, 7, 31892–31906. Available online: https://pubmed.ncbi.nlm.nih.gov/26895469 (accessed on 20 December 2021). [CrossRef] [PubMed]
  127. Huse, J.T.; Holland, E.C. Targeting brain cancer: Advances in the molecular pathology of malignant glioma and medulloblastoma. Nat. Rev. Cancer 2010, 10, 319–331. [Google Scholar] [CrossRef] [PubMed]
  128. Wullschleger, S.; Loewith, R.; Hall, M.N. Tor signaling in growth and metabolism. Cell 2006, 124, 471–484. [Google Scholar] [CrossRef] [Green Version]
  129. Shimobayashi, M.; Hall, M.N. Making new contacts: The mtor network in metabolism and signalling crosstalk. Nat. Rev. Mol. Cell Biol. 2014, 15, 155–162. [Google Scholar] [CrossRef]
  130. Shahbazian, D.; Roux, P.P.; Mieulet, V.; Cohen, M.S.; Raught, B.; Taunton, J.; Hershey, J.W.B.; Blenis, J.; Pende, M.; Sonenberg, N. The mtor/pi3k and mapk pathways converge on eif4b to control its phosphorylation and activity. EMBO J. 2006, 25, 2781–2791. [Google Scholar] [CrossRef]
  131. Meyuhas, O. Physiological roles of ribosomal protein s6: One of its kind. Int. Rev. Cell Mol. Biol. 2008, 268, 1–37. [Google Scholar]
  132. Ruvinsky, I.; Katz, M.; Dreazen, A.; Gielchinsky, Y.; Saada, A.; Freedman, N.; Mishani, E.; Zimmerman, G.; Kasir, J.; Meyuhas, O. Mice deficient in ribosomal protein s6 phosphorylation suffer from muscle weakness that reflects a growth defect and energy deficit. PLoS ONE 2009, 4, e5618. [Google Scholar] [CrossRef] [Green Version]
  133. Xu, J.; Chen, J.; Dong, Z.; Meyuhas, O.; Chen, J.K. Phosphorylation of ribosomal protein s6 mediates compensatory renal hypertrophy. Kidney Int. 2015, 87, 543–556. [Google Scholar] [CrossRef] [Green Version]
  134. Volovelsky, O.; Cohen, G.; Kenig, A.; Wasserman, G.; Dreazen, A.; Meyuhas, O.; Silver, J.; Naveh-Many, T. Phosphorylation of ribosomal protein s6 mediates mammalian target of rapamycin complex 1-induced parathyroid cell proliferation in secondary hyperparathyroidism. J. Am. Soc. Nephrol. 2016, 27, 1091–1101. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/26283674 (accessed on 20 December 2021). [CrossRef] [PubMed] [Green Version]
  135. Tan, X.; Wen, X.; Liu, Y. Paricalcitol inhibits renal inflammation by promoting vitamin d receptor-mediated sequestration of nf-kappab signaling. J. Am. Soc. Nephrol. 2008, 19, 1741–1752. Available online: https://pubmed.ncbi.nlm.nih.gov/18525004 (accessed on 20 December 2021). [CrossRef] [PubMed] [Green Version]
  136. Delfino, F.; Walker, W.H. Hormonal regulation of the nf-kappab signaling pathway. Mol. Cell Endocrinol. 1999, 157, 1–9. [Google Scholar] [CrossRef]
  137. Nakanishi, C.; Toi, M. Nuclear factor-kappab inhibitors as sensitizers to anticancer drugs. Nat. Rev. Cancer 2005, 5, 297–309. [Google Scholar] [CrossRef] [PubMed]
  138. Guttridge, D.C.; Albanese, C.; Reuther, J.Y.; Pestell, R.G.; Baldwin, A.S.J. Nf-kappab controls cell growth and differentiation through transcriptional regulation of cyclin d1. Mol. Cell Biol. 1999, 19, 5785–5799. [Google Scholar] [CrossRef] [Green Version]
  139. Heppner, C.; Bilimoria, K.Y.; Agarwal, S.K.; Kester, M.; Whitty, L.J.; Guru, S.C.; Chandrasekharappa, S.C.; Collins, F.S.; Spiegel, A.M.; Marx, S.J.; et al. The tumor suppressor protein menin interacts with nf-κb proteins and inhibits nf-κb-mediated transactivation. Oncogene 2001, 20, 4917–4925. [Google Scholar] [CrossRef] [Green Version]
  140. Corbetta, S.; Vicentini, L.; Ferrero, S.; Lania, A.; Mantovani, G.; Cordella, D.; Beck-Peccoz, P.; Spada, A. Activity and function of the nuclear factor kappab pathway in human parathyroid tumors. Endocr. Relat. Cancer 2005, 12, 929–937. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/16322332 (accessed on 20 December 2021). [CrossRef]
  141. Kan, S.; Zhang, W.; Mao, J.; Wang, M.; Ni, L.; Zhang, M.; Zhang, Q.; Chen, J. Nf-κb activation contributes to parathyroid cell proliferation in chronic kidney disease. J. Nephrol. 2018, 31, 941–951. [Google Scholar] [CrossRef]
  142. Mann, J.R.; Backlund, M.G.; DuBois, R.N. Mechanisms of disease: Inflammatory mediators and cancer prevention. Nat. Clin. Pract. Oncol. 2005, 2, 202–210. [Google Scholar] [CrossRef]
  143. Bell, C.D.; Vidal, S.; Kovacs, K.; Anderson, J.; Rotondo, F. Cox-2 expression in the oxyphilic cells of the normal, hyperplastic, and adenomatous parathyroid gland. Endocr. Pathol. 2004, 15, 29–38. [Google Scholar] [CrossRef]
  144. Zhang, Q.; Qiu, J.; Li, H.; Lu, Y.; Wang, X.; Yang, J.; Wang, S.; Zhang, L.; Gu, Y.; Hao, C.-M.; et al. Cyclooxygenase 2 promotes parathyroid hyperplasia in esrd. J. Am. Soc. Nephrol. 2011, 22, 664–672. Available online: https://pubmed.ncbi.nlm.nih.gov/21335517 (accessed on 20 December 2021). [CrossRef] [PubMed] [Green Version]
  145. Gardner, D.G.; Brown, E.M.; Windeck, R.; Aurbach, G.D. Prostaglandin e2 inhibits 3′,5′-adenosine monophosphate accumulation and parathyroid hormone release from dispersed bovine parathyroid cells. Endocrinology 1979, 104, 1–7. [Google Scholar] [CrossRef] [PubMed]
  146. Gardner, D.G.; Brown, E.M.; Attie, M.F.; Aurbach, G.D. Prostaglandin-mediated stimulation of adenosine 3′,5′-monophosphate accumulation and parathyroid hormone release in dispersed human parathyroid cells. J. Clin. Endocrinol. Metab. 1980, 51, 20–25. [Google Scholar] [CrossRef] [PubMed]
  147. Zhang, Q.; Li, S.; Ye, G.; Wang, M.; Ni, L.; Kan, S.; Zhang, M.; Chen, J. Prostaglandin e2 receptor ep2 mediates the effect of cyclooxygenase 2 on secondary parathyroid hyperplasia in end-stage renal disease. Nephrol. Dial. Transplant. 2019, 34, 606–617. [Google Scholar] [CrossRef] [PubMed]
  148. Gekakis, N.; Staknis, D.; Nguyen, H.B.; Davis, F.C.; Wilsbacher, L.D.; King, D.P.; Takahashi, J.S.; Weitz, C.J. Role of the clock protein in the mammalian circadian mechanism. Science 1998, 280, 1564–1569. [Google Scholar] [CrossRef] [PubMed]
  149. Kim, M.S.; Fujiki, R.; Murayama, A.; Kitagawa, H.; Yamaoka, K.; Yamamoto, Y.; Mihara, M.; Takeyama, K.; Kato, S. 1alpha,25(oh)2d3-induced transrepression by vitamin d receptor through e-box-type elements in the human parathyroid hormone gene promoter. Mol. Endocrinol. 2007, 21, 334–342. Available online: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/pubmed/17095575 (accessed on 20 December 2021). [CrossRef]
  150. Egstrand, S.; Nordholm, A.; Morevati, M.; Mace, M.L.; Hassan, A.; Naveh-Many, T.; Rukov, J.L.; Gravesen, E.; Olgaard, K.; Lewin, E. A molecular circadian clock operates in the parathyroid gland and is disturbed in chronic kidney disease associated bone and mineral disorder. Kidney Int. 2020, 98, 1461–1475. Available online: https://0-www-sciencedirect-com.brum.beds.ac.uk/science/article/pii/S0085253820308280 (accessed on 20 December 2021). [CrossRef]
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Figure 1. Model for the regulation of PTH mRNA stability in SHP by protein–PTH mRNA interactions and Pin1. Basal PTH mRNA levels are determined by a balanced interaction of the PTH mRNA 3′-UTR ARE with its stabilizing protein AUF1 and destabilizing protein KSRP that recruits the exosome (Pac-Man) to mRNAs. The isomerase Pin1 binds KSRP and induces KSRP Ser181 conformational change and dephosphorylation, which increases KSRP-PTH mRNA interaction and mRNA decay. In SHP, due to kidney failure or hypocalcemia, there is decreased parathyroid Pin1 isomerase activity and phosphorylated KSRP fails to bind PTH mRNA and recruit the exosome to it. As a result, AUF1 binds PTH mRNA with greater affinity, leading to increased PTH mRNA stability and levels. Schematic representation of the PTH mRNA with the coding sequence (CDS) in brown, the 5′- and 3′-untranslated regions (UTRs) in orange and ARE in red. AUF1, AU-rich binding factor 1; KSRP, K-homology splicing regulatory protein. Adapted with permission from the FASEB Journal [26].
Figure 1. Model for the regulation of PTH mRNA stability in SHP by protein–PTH mRNA interactions and Pin1. Basal PTH mRNA levels are determined by a balanced interaction of the PTH mRNA 3′-UTR ARE with its stabilizing protein AUF1 and destabilizing protein KSRP that recruits the exosome (Pac-Man) to mRNAs. The isomerase Pin1 binds KSRP and induces KSRP Ser181 conformational change and dephosphorylation, which increases KSRP-PTH mRNA interaction and mRNA decay. In SHP, due to kidney failure or hypocalcemia, there is decreased parathyroid Pin1 isomerase activity and phosphorylated KSRP fails to bind PTH mRNA and recruit the exosome to it. As a result, AUF1 binds PTH mRNA with greater affinity, leading to increased PTH mRNA stability and levels. Schematic representation of the PTH mRNA with the coding sequence (CDS) in brown, the 5′- and 3′-untranslated regions (UTRs) in orange and ARE in red. AUF1, AU-rich binding factor 1; KSRP, K-homology splicing regulatory protein. Adapted with permission from the FASEB Journal [26].
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Figure 2. Protein–mRNA interactions and miRNA determine the post-transcriptional increase in parathyroid hormone (PTH) gene expression in SHP. Decreased activity of the isomerase Pin1 in the parathyroid in SHP modifies protein–PTH mRNA interactions to increase PTH mRNA stability and levels in experimental chronic kidney failure. The stimulation of PTH expression is also dependent upon miRNA. Parathyroid miRNAs are dysregulated in both chronic kidney disease patients and experimental models. Mice with parathyroid specific knockout of Dicer, which prevents global miRNA maturation and function, fail to increase serum PTH after acute and chronic hypocalcemia or uremia, demonstrating that miRNAs are essential for parathyroid stimulation in SHP. Let-7 and miR-148 miRNA families that are dysregulated in CKD-SHP modify PTH secretion in vivo and in vitro, suggesting roles for these miRNAs in the increased PTH expression.
Figure 2. Protein–mRNA interactions and miRNA determine the post-transcriptional increase in parathyroid hormone (PTH) gene expression in SHP. Decreased activity of the isomerase Pin1 in the parathyroid in SHP modifies protein–PTH mRNA interactions to increase PTH mRNA stability and levels in experimental chronic kidney failure. The stimulation of PTH expression is also dependent upon miRNA. Parathyroid miRNAs are dysregulated in both chronic kidney disease patients and experimental models. Mice with parathyroid specific knockout of Dicer, which prevents global miRNA maturation and function, fail to increase serum PTH after acute and chronic hypocalcemia or uremia, demonstrating that miRNAs are essential for parathyroid stimulation in SHP. Let-7 and miR-148 miRNA families that are dysregulated in CKD-SHP modify PTH secretion in vivo and in vitro, suggesting roles for these miRNAs in the increased PTH expression.
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Figure 3. Regulators of PTH gene expression and parathyroid cell proliferation in SHP. Hyperphosphatemia and hypocalcemia stimulate and 1,25(OH)2 vitamin D (1,25D) and fibroblast growth factor (FGF) 23 inhibit PTH production and parathyroid cell proliferation. In CKD-induced SHP, decreased expression of the CaSR, VDR and FGFR-klotho receptors together with activation of mTOR, TGF-α-EGFR and Cox-PGE2 signaling and changes in cell cycle regulators lead to hyperplastic parathyroid glands with high serum PTH levels. In the parathyroid cell, protein–PTH mRNA interactions mediated by activity of the isomerase Pin1 and miRNA increase PTH production and secretion. Adapted with permission from the International Journal of Molecular Sciences [99].
Figure 3. Regulators of PTH gene expression and parathyroid cell proliferation in SHP. Hyperphosphatemia and hypocalcemia stimulate and 1,25(OH)2 vitamin D (1,25D) and fibroblast growth factor (FGF) 23 inhibit PTH production and parathyroid cell proliferation. In CKD-induced SHP, decreased expression of the CaSR, VDR and FGFR-klotho receptors together with activation of mTOR, TGF-α-EGFR and Cox-PGE2 signaling and changes in cell cycle regulators lead to hyperplastic parathyroid glands with high serum PTH levels. In the parathyroid cell, protein–PTH mRNA interactions mediated by activity of the isomerase Pin1 and miRNA increase PTH production and secretion. Adapted with permission from the International Journal of Molecular Sciences [99].
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Hassan, A.; Khalaily, N.; Kilav-Levin, R.; Nechama, M.; Volovelsky, O.; Silver, J.; Naveh-Many, T. Molecular Mechanisms of Parathyroid Disorders in Chronic Kidney Disease. Metabolites 2022, 12, 111. https://0-doi-org.brum.beds.ac.uk/10.3390/metabo12020111

AMA Style

Hassan A, Khalaily N, Kilav-Levin R, Nechama M, Volovelsky O, Silver J, Naveh-Many T. Molecular Mechanisms of Parathyroid Disorders in Chronic Kidney Disease. Metabolites. 2022; 12(2):111. https://0-doi-org.brum.beds.ac.uk/10.3390/metabo12020111

Chicago/Turabian Style

Hassan, Alia, Nareman Khalaily, Rachel Kilav-Levin, Morris Nechama, Oded Volovelsky, Justin Silver, and Tally Naveh-Many. 2022. "Molecular Mechanisms of Parathyroid Disorders in Chronic Kidney Disease" Metabolites 12, no. 2: 111. https://0-doi-org.brum.beds.ac.uk/10.3390/metabo12020111

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