Extracellular Vesicles in Urogenital Cancers

A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Tumor Microenvironment".

Deadline for manuscript submissions: closed (6 June 2022) | Viewed by 3233

Special Issue Editors


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Guest Editor
University Lyon, Université. Claude Bernard Lyon 1, CNRS UMR 5246, ICBMS, F-69622 Lyon, France
Interests: lipid signaling and signal transduction; prostate cancer; bone metastasis; vascular calcification; atherosclerosis; extracellular vesicles
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
University Lyon, Université. Claude Bernard Lyon 1, CNRS UMR 5246, ICBMS, F-69622 Lyon, France
Interests: lipid signaling and signal transduction; prostate cancer; bone metastasis; vascular calcification; atherosclerosis; extracellular vesicles
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

It is now widely admitted that cancer cells strongly interact with their surrounding cells, and extracellular vesicles (EV) emerge as new players in the regulation of the tumor microenvironment. EVs have been historically classified on the basis or their size. Endosome-origin exosomes are small (30-150 nm in diameter) extracellular nanovesicles containing miRNAs, mRNAs, DNAs, proteins, lipids among others. Microvesicles (MVs) (100-1000 nm in diameter) are generated directly from the plasma membrane by budding. Some studies report a third class of EVs, the apoptotic bodies (ABs), which are large EVs (often >1000 nm in diameter). ABs are implicated in cell signaling but they are not always considered as EV as they are only secreted during a very precise context, programmed cell death. This Special Issue will highlight the implication of EVs in the pathophysiology of urogenital cancers (kidney, prostate, bladder, testicle, head & neck, ovarian cancer). Notably, the role of EVs and their components in tumorigenesis of primary tumor cells and in the onset and dissemination of metastasis will be described. Other functions of EVs, for example as diagnostic tools or predictors of disease outcome could be explained. Finally, the description of the later literature and novel findings will be much appreciated.

Dr. Leyre Brizuela
Dr. Mebarek Saida
Guest Editors

Manuscript Submission Information

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Keywords

  • Extracellular Vesicles
  • Exosomes
  • Microvesicles
  • Lipid Signaling
  • Kidney
  • Prostate
  • Bone Metastasis

Published Papers (1 paper)

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Research

13 pages, 555 KiB  
Article
Determination of Exosome Mitochondrial DNA as a Biomarker of Renal Cancer Aggressiveness
by Elena Arance, Viviana Ramírez, Alejandro Rubio-Roldan, Francisco M. Ocaña-Peinado, Catalina Romero-Cachinero, Ana Belén Jódar-Reyes, Fernando Vazquez-Alonso, Luis Javier Martinez-Gonzalez and Maria Jesus Alvarez-Cubero
Cancers 2022, 14(1), 199; https://0-doi-org.brum.beds.ac.uk/10.3390/cancers14010199 - 31 Dec 2021
Cited by 19 | Viewed by 2799
Abstract
Here, the role of non-invasive biomarkers in liquid biopsy was evaluated, mainly in exosomes and mitochondrial DNA (mtDNA) as promising, novel, and stable biomarkers for renal cell carcinoma (RCC). A total of 140 fractions (named from B to F) obtained by ultracentrifugations of [...] Read more.
Here, the role of non-invasive biomarkers in liquid biopsy was evaluated, mainly in exosomes and mitochondrial DNA (mtDNA) as promising, novel, and stable biomarkers for renal cell carcinoma (RCC). A total of 140 fractions (named from B to F) obtained by ultracentrifugations of whole blood samples from 28 individuals (13 patients and 15 controls) were included. Nanoparticle Tracking Analysis (NTA) was conducted to characterized exosomal fraction. Subsequently, an analysis of digital PCR (dPCR) using the QuantStudio™ 3D Digital PCR platform was performed and the quantification of mtDNA copy number by QuantStudioTM 12K Flex Real-Time PCR System (qPCR) was developed. Moreover, Next Generation Sequencing (NGS) analyses were included using MiSeq system (Illumina, San Diego, CA, USA). An F fraction, which contains all exosome data and all mitochondrial markers, was identified in dPCR and qPCR with statistically significant power (adjusted p values ≤ 0.03) when comparing cases and controls. Moreover, present analysis in mtDNA showed a relevant significance in RCC aggressiveness. To sum up, this is the first time a relation between exosomal mtDNA markers and clinical management of RCC is analyzed. We suggest a promising strategy for future liquid biopsy RCC analysis, although more analysis should be performed prior to application in routine clinical practice. Full article
(This article belongs to the Special Issue Extracellular Vesicles in Urogenital Cancers)
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