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Combination Treatment Strategies to Overcome PARP Inhibitor Resistance
Poly(ADP-ribose) polymerase (PARP) enzymes have been shown to be essential for DNA repair pathways, including homologous recombination repair (HRR). Cancers with HRR defects (e.g., BRCA1 and BRCA2 mutations) are targets for PARP inhibitors (PARPis) based on the exploitation of “synthetic lethality”....
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10604269/ https://www.ncbi.nlm.nih.gov/pubmed/37892162 http://dx.doi.org/10.3390/biom13101480 |
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author | Soung, Young-Hwa Chung, Jun |
author_facet | Soung, Young-Hwa Chung, Jun |
author_sort | Soung, Young-Hwa |
collection | PubMed |
description | Poly(ADP-ribose) polymerase (PARP) enzymes have been shown to be essential for DNA repair pathways, including homologous recombination repair (HRR). Cancers with HRR defects (e.g., BRCA1 and BRCA2 mutations) are targets for PARP inhibitors (PARPis) based on the exploitation of “synthetic lethality”. As a result, PARPis offer a promising treatment option for advanced ovarian and breast cancers with deficiencies in HRR. However, acquired resistance to PARPis has been reported for most tumors, and not all patients with BRCA1/2 mutations respond to PARPis. Therefore, the formulation of effective treatment strategies to overcome resistance to PARPis is urgently necessary. This review summarizes the molecular mechanism of therapeutic action and resistance to PARPis, in addition to emerging combination treatment options involving PARPis. |
format | Online Article Text |
id | pubmed-10604269 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106042692023-10-28 Combination Treatment Strategies to Overcome PARP Inhibitor Resistance Soung, Young-Hwa Chung, Jun Biomolecules Review Poly(ADP-ribose) polymerase (PARP) enzymes have been shown to be essential for DNA repair pathways, including homologous recombination repair (HRR). Cancers with HRR defects (e.g., BRCA1 and BRCA2 mutations) are targets for PARP inhibitors (PARPis) based on the exploitation of “synthetic lethality”. As a result, PARPis offer a promising treatment option for advanced ovarian and breast cancers with deficiencies in HRR. However, acquired resistance to PARPis has been reported for most tumors, and not all patients with BRCA1/2 mutations respond to PARPis. Therefore, the formulation of effective treatment strategies to overcome resistance to PARPis is urgently necessary. This review summarizes the molecular mechanism of therapeutic action and resistance to PARPis, in addition to emerging combination treatment options involving PARPis. MDPI 2023-10-03 /pmc/articles/PMC10604269/ /pubmed/37892162 http://dx.doi.org/10.3390/biom13101480 Text en © 2023 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 Soung, Young-Hwa Chung, Jun Combination Treatment Strategies to Overcome PARP Inhibitor Resistance |
title | Combination Treatment Strategies to Overcome PARP Inhibitor Resistance |
title_full | Combination Treatment Strategies to Overcome PARP Inhibitor Resistance |
title_fullStr | Combination Treatment Strategies to Overcome PARP Inhibitor Resistance |
title_full_unstemmed | Combination Treatment Strategies to Overcome PARP Inhibitor Resistance |
title_short | Combination Treatment Strategies to Overcome PARP Inhibitor Resistance |
title_sort | combination treatment strategies to overcome parp inhibitor resistance |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10604269/ https://www.ncbi.nlm.nih.gov/pubmed/37892162 http://dx.doi.org/10.3390/biom13101480 |
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