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Epigenetic Mechanisms Involved in Cisplatin-Induced Nephrotoxicity: An Update

Cisplatin is an antineoplastic drug used for the treatment of many solid tumors. Among its various side effects, nephrotoxicity is the most detrimental. In recent years, epigenetic regulation has emerged as a modulatory mechanism of cisplatin-induced nephrotoxicity, involving non-coding RNAs, DNA me...

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Autores principales: Loren, Pía, Saavedra, Nicolás, Saavedra, Kathleen, Zambrano, Tomás, Moriel, Patricia, Salazar, Luis A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8223972/
https://www.ncbi.nlm.nih.gov/pubmed/34063951
http://dx.doi.org/10.3390/ph14060491
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author Loren, Pía
Saavedra, Nicolás
Saavedra, Kathleen
Zambrano, Tomás
Moriel, Patricia
Salazar, Luis A.
author_facet Loren, Pía
Saavedra, Nicolás
Saavedra, Kathleen
Zambrano, Tomás
Moriel, Patricia
Salazar, Luis A.
author_sort Loren, Pía
collection PubMed
description Cisplatin is an antineoplastic drug used for the treatment of many solid tumors. Among its various side effects, nephrotoxicity is the most detrimental. In recent years, epigenetic regulation has emerged as a modulatory mechanism of cisplatin-induced nephrotoxicity, involving non-coding RNAs, DNA methylation and histone modifications. These epigenetic marks alter different signaling pathways leading to damage and cell death. In this review, we describe how different epigenetic modifications alter different pathways leading to cell death by apoptosis, autophagy, necroptosis, among others. The study of epigenetic regulation is still under development, and much research remains to fully determine the epigenetic mechanisms underlying cell death, which will allow leading new strategies for the diagnosis and therapy of this disease.
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spelling pubmed-82239722021-06-25 Epigenetic Mechanisms Involved in Cisplatin-Induced Nephrotoxicity: An Update Loren, Pía Saavedra, Nicolás Saavedra, Kathleen Zambrano, Tomás Moriel, Patricia Salazar, Luis A. Pharmaceuticals (Basel) Review Cisplatin is an antineoplastic drug used for the treatment of many solid tumors. Among its various side effects, nephrotoxicity is the most detrimental. In recent years, epigenetic regulation has emerged as a modulatory mechanism of cisplatin-induced nephrotoxicity, involving non-coding RNAs, DNA methylation and histone modifications. These epigenetic marks alter different signaling pathways leading to damage and cell death. In this review, we describe how different epigenetic modifications alter different pathways leading to cell death by apoptosis, autophagy, necroptosis, among others. The study of epigenetic regulation is still under development, and much research remains to fully determine the epigenetic mechanisms underlying cell death, which will allow leading new strategies for the diagnosis and therapy of this disease. MDPI 2021-05-21 /pmc/articles/PMC8223972/ /pubmed/34063951 http://dx.doi.org/10.3390/ph14060491 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Loren, Pía
Saavedra, Nicolás
Saavedra, Kathleen
Zambrano, Tomás
Moriel, Patricia
Salazar, Luis A.
Epigenetic Mechanisms Involved in Cisplatin-Induced Nephrotoxicity: An Update
title Epigenetic Mechanisms Involved in Cisplatin-Induced Nephrotoxicity: An Update
title_full Epigenetic Mechanisms Involved in Cisplatin-Induced Nephrotoxicity: An Update
title_fullStr Epigenetic Mechanisms Involved in Cisplatin-Induced Nephrotoxicity: An Update
title_full_unstemmed Epigenetic Mechanisms Involved in Cisplatin-Induced Nephrotoxicity: An Update
title_short Epigenetic Mechanisms Involved in Cisplatin-Induced Nephrotoxicity: An Update
title_sort epigenetic mechanisms involved in cisplatin-induced nephrotoxicity: an update
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8223972/
https://www.ncbi.nlm.nih.gov/pubmed/34063951
http://dx.doi.org/10.3390/ph14060491
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