Predictors and Modulators of Synthetic Lethality: An Update on PARP Inhibitors and Personalized Medicine

Poly(ADP-ribose) polymerase (PARP) inhibitors have proven to be successful agents in inducing synthetic lethality in several malignancies. Several PARP inhibitors have reached clinical trial testing for treatment in different cancers, and, recently, Olaparib (AZD2281) has gained both United States F...

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Main Authors: Stephen Murata, Catherine Zhang, Nathan Finch, Kevin Zhang, Loredana Campo, Eun-Kyoung Breuer
Format: Article
Language:English
Published: Hindawi Limited 2016-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2016/2346585
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spelling doaj-f710a9c31d1c4c458ab4c2cfcd298a2f2020-11-24T21:18:34ZengHindawi LimitedBioMed Research International2314-61332314-61412016-01-01201610.1155/2016/23465852346585Predictors and Modulators of Synthetic Lethality: An Update on PARP Inhibitors and Personalized MedicineStephen Murata0Catherine Zhang1Nathan Finch2Kevin Zhang3Loredana Campo4Eun-Kyoung Breuer5Department of Radiation Oncology, Stritch School of Medicine, Loyola University Chicago, Maywood, IL 60153, USADepartment of Radiation Oncology, Stritch School of Medicine, Loyola University Chicago, Maywood, IL 60153, USADepartment of Radiation Oncology, Stritch School of Medicine, Loyola University Chicago, Maywood, IL 60153, USADepartment of Otorhinolaryngology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USADepartment of Radiation Oncology, Stritch School of Medicine, Loyola University Chicago, Maywood, IL 60153, USADepartment of Radiation Oncology, Stritch School of Medicine, Loyola University Chicago, Maywood, IL 60153, USAPoly(ADP-ribose) polymerase (PARP) inhibitors have proven to be successful agents in inducing synthetic lethality in several malignancies. Several PARP inhibitors have reached clinical trial testing for treatment in different cancers, and, recently, Olaparib (AZD2281) has gained both United States Food and Drug Administration (USFDA) and the European Commission (EC) approval for use in BRCA-mutated advanced ovarian cancer treatment. The need to identify biomarkers, their interactions in DNA damage repair pathways, and their potential utility in identifying patients who are candidates for PARP inhibitor treatment is well recognized. In this review, we detail many of the biomarkers that have been investigated for their ability to predict both PARP inhibitor sensitivity and resistance in preclinical studies as well as the results of several clinical trials that have tested the safety and efficacy of different PARP inhibitor agents in BRCA and non-BRCA-mutated cancers.http://dx.doi.org/10.1155/2016/2346585
collection DOAJ
language English
format Article
sources DOAJ
author Stephen Murata
Catherine Zhang
Nathan Finch
Kevin Zhang
Loredana Campo
Eun-Kyoung Breuer
spellingShingle Stephen Murata
Catherine Zhang
Nathan Finch
Kevin Zhang
Loredana Campo
Eun-Kyoung Breuer
Predictors and Modulators of Synthetic Lethality: An Update on PARP Inhibitors and Personalized Medicine
BioMed Research International
author_facet Stephen Murata
Catherine Zhang
Nathan Finch
Kevin Zhang
Loredana Campo
Eun-Kyoung Breuer
author_sort Stephen Murata
title Predictors and Modulators of Synthetic Lethality: An Update on PARP Inhibitors and Personalized Medicine
title_short Predictors and Modulators of Synthetic Lethality: An Update on PARP Inhibitors and Personalized Medicine
title_full Predictors and Modulators of Synthetic Lethality: An Update on PARP Inhibitors and Personalized Medicine
title_fullStr Predictors and Modulators of Synthetic Lethality: An Update on PARP Inhibitors and Personalized Medicine
title_full_unstemmed Predictors and Modulators of Synthetic Lethality: An Update on PARP Inhibitors and Personalized Medicine
title_sort predictors and modulators of synthetic lethality: an update on parp inhibitors and personalized medicine
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2016-01-01
description Poly(ADP-ribose) polymerase (PARP) inhibitors have proven to be successful agents in inducing synthetic lethality in several malignancies. Several PARP inhibitors have reached clinical trial testing for treatment in different cancers, and, recently, Olaparib (AZD2281) has gained both United States Food and Drug Administration (USFDA) and the European Commission (EC) approval for use in BRCA-mutated advanced ovarian cancer treatment. The need to identify biomarkers, their interactions in DNA damage repair pathways, and their potential utility in identifying patients who are candidates for PARP inhibitor treatment is well recognized. In this review, we detail many of the biomarkers that have been investigated for their ability to predict both PARP inhibitor sensitivity and resistance in preclinical studies as well as the results of several clinical trials that have tested the safety and efficacy of different PARP inhibitor agents in BRCA and non-BRCA-mutated cancers.
url http://dx.doi.org/10.1155/2016/2346585
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