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Platinum Resistance in Ovarian Cancer: Role of DNA Repair

Epithelial ovarian cancer (EOC) is the most lethal gynecological cancer. It is initially responsive to cisplatin and carboplatin, two DNA damaging agents used in first line therapy. However, almost invariably, patients relapse with a tumor resistant to subsequent treatment with platinum containing d...

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Detalles Bibliográficos
Autores principales: Damia, Giovanna, Broggini, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357127/
https://www.ncbi.nlm.nih.gov/pubmed/30669514
http://dx.doi.org/10.3390/cancers11010119
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author Damia, Giovanna
Broggini, Massimo
author_facet Damia, Giovanna
Broggini, Massimo
author_sort Damia, Giovanna
collection PubMed
description Epithelial ovarian cancer (EOC) is the most lethal gynecological cancer. It is initially responsive to cisplatin and carboplatin, two DNA damaging agents used in first line therapy. However, almost invariably, patients relapse with a tumor resistant to subsequent treatment with platinum containing drugs. Several mechanisms associated with the development of acquired drug resistance have been reported. Here we focused our attention on DNA repair mechanisms, which are fundamental for recognition and removal of platinum adducts and hence for the ability of these drugs to exert their activity. We analyzed the major DNA repair pathways potentially involved in drug resistance, detailing gene mutation, duplication or deletion as well as polymorphisms as potential biomarkers for drug resistance development. We dissected potential ways to overcome DNA repair-associated drug resistance thanks to the development of new combinations and/or drugs directly targeting DNA repair proteins or taking advantage of the vulnerability arising from DNA repair defects in EOCs.
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spelling pubmed-63571272019-02-05 Platinum Resistance in Ovarian Cancer: Role of DNA Repair Damia, Giovanna Broggini, Massimo Cancers (Basel) Review Epithelial ovarian cancer (EOC) is the most lethal gynecological cancer. It is initially responsive to cisplatin and carboplatin, two DNA damaging agents used in first line therapy. However, almost invariably, patients relapse with a tumor resistant to subsequent treatment with platinum containing drugs. Several mechanisms associated with the development of acquired drug resistance have been reported. Here we focused our attention on DNA repair mechanisms, which are fundamental for recognition and removal of platinum adducts and hence for the ability of these drugs to exert their activity. We analyzed the major DNA repair pathways potentially involved in drug resistance, detailing gene mutation, duplication or deletion as well as polymorphisms as potential biomarkers for drug resistance development. We dissected potential ways to overcome DNA repair-associated drug resistance thanks to the development of new combinations and/or drugs directly targeting DNA repair proteins or taking advantage of the vulnerability arising from DNA repair defects in EOCs. MDPI 2019-01-20 /pmc/articles/PMC6357127/ /pubmed/30669514 http://dx.doi.org/10.3390/cancers11010119 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Damia, Giovanna
Broggini, Massimo
Platinum Resistance in Ovarian Cancer: Role of DNA Repair
title Platinum Resistance in Ovarian Cancer: Role of DNA Repair
title_full Platinum Resistance in Ovarian Cancer: Role of DNA Repair
title_fullStr Platinum Resistance in Ovarian Cancer: Role of DNA Repair
title_full_unstemmed Platinum Resistance in Ovarian Cancer: Role of DNA Repair
title_short Platinum Resistance in Ovarian Cancer: Role of DNA Repair
title_sort platinum resistance in ovarian cancer: role of dna repair
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357127/
https://www.ncbi.nlm.nih.gov/pubmed/30669514
http://dx.doi.org/10.3390/cancers11010119
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