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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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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