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Molecular Mechanisms and Biomarkers in Drug-Associated Organ Injury

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Pathology, Diagnostics, and Therapeutics".

Deadline for manuscript submissions: closed (15 July 2022) | Viewed by 3645

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Guest Editor
Division of Clinical Pharmaceutics, Department of Pharmaceutical Health Care, Faculty of Pharmaceutical Sciences, Himeji Dokkyo University, Himeji 670-0896, Japan
Interests: biomarker; nephrology; pharmacogenomics; immunosuppressive drugs; drug transporter; liver transplantation; kidney transplantation; inflammatory bowel disease; antiinfective agent; therapeutic drug monitoring
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Special Issue Information

Dear Colleagues,

Biomarkers reflecting, predicting, and associating pharmacological effects and/or toxicological disorders have been widely examined. Candidate molecules that act as potential biomarkers for drug-induced organ toxicity have been discovered. Endogenous compounds are well-applied in the clinical setting, such as creatinine, Na+, blood urea nitrogen, aminotransferase, bilirubin, and so on. Despite these classical markers, some peptides and miRNAs have been examined as new types of biomarkers.

In the field of nephrotoxicity, serum creatinine is usually examined for use as a conventional marker for renal damage in clinical treatment. However, this biochemical parameter is acknowledged to be non-specific to cover drug-induced kidney injury. Similar to kidney injury, drug-induced liver, lung, and bone marrow injury are often observed in pharmacotherapy and chemotherapy. Therefore, some organ-specific and/or drug-specific biological markers including functional proteins, peptides, nucleic acids, fatty acids, miRNAs, and so on are required to make accurate diagnosis.

Recently, the research area of biomarkers in pharmacology and toxicology has been expanded to find the physiological and pathophysiological significance in molecular-biological processes. With these exciting findings, this Special issue focuses on “Molecular Mechanisms and Biomarkers in Drug-Associated Organ Injury”.

Prof. Dr. Satohiro Masuda
Guest Editor

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Keywords

  • molecular mechanisms and biomarkers in drug-associated kidney injury
  • molecular mechanisms and biomarkers in drug-associated liver injury
  • molecular mechanisms and biomarkers in drug-associated lung injury
  • molecular mechanisms and biomarkers in drug-associated neuropathy
  • molecular mechanisms and biomarkers in drug-associated bone marrow injury
  • cancer chemotherapy
  • anti-infectious treatment
  • immunosuppressive drugs
  • anti-diabetic drugs
  • cardiovascular treatment
  • anti-inflammatory bowel disease
  • treatment against autoimmune disease

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Published Papers (1 paper)

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Review

23 pages, 1932 KiB  
Review
Molecular Mechanisms and Biomarkers Associated with Chemotherapy-Induced AKI
by Letizia De Chiara, Gianmarco Lugli, Gianluca Villa, Valentina Raglianti, Faeq Husain-Syed, Fiammetta Ravaglia, Paola Romagnani and Elena Lazzeri
Int. J. Mol. Sci. 2022, 23(5), 2638; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms23052638 - 27 Feb 2022
Cited by 7 | Viewed by 2974
Abstract
Acute kidney injury (AKI) is a life-threatening condition characterized by a rapid and transient decrease in kidney function. AKI is part of an array of conditions collectively defined as acute kidney diseases (AKD). In AKD, persistent kidney damage and dysfunction lead to chronic [...] Read more.
Acute kidney injury (AKI) is a life-threatening condition characterized by a rapid and transient decrease in kidney function. AKI is part of an array of conditions collectively defined as acute kidney diseases (AKD). In AKD, persistent kidney damage and dysfunction lead to chronic kidney disease (CKD) over time. A variety of insults can trigger AKI; however, chemotherapy-associated nephrotoxicity is increasingly recognized as a significant side effect of chemotherapy. New biomarkers are urgently needed to identify patients at high risk of developing chemotherapy-associated nephrotoxicity and subsequent AKI. However, a lack of understanding of cellular mechanisms that trigger chemotherapy-related nephrotoxicity has hindered the identification of effective biomarkers to date. In this review, we aim to (1) describe the known and potential mechanisms related to chemotherapy-induced AKI; (2) summarize the available biomarkers for early AKI detection, and (3) raise awareness of chemotherapy-induced AKI. Full article
(This article belongs to the Special Issue Molecular Mechanisms and Biomarkers in Drug-Associated Organ Injury)
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