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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”....

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Detalles Bibliográficos
Autores principales: Soung, Young-Hwa, Chung, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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.
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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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