PARP-ish: Gaps in Molecular Understanding and Clinical Trials Targeting PARP Exacerbate Racial Disparities in Prostate Cancer

被引:0
作者
Cunningham, Moriah L. [1 ,3 ]
Schiewer, Matthew J. [1 ,2 ,3 ]
机构
[1] Thomas Jefferson Univ, Dept Urol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Dept Pharmacol Physiol & Canc Biol, Philadelphia, PA 19107 USA
[3] Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Philadelphia, PA 19107 USA
关键词
DNA-REPAIR; AFRICAN-AMERICAN; POLY(ADP-RIBOSE) POLYMERASE-1; ADP-RIBOSYLATION; BREAST-CANCER; INHIBITORS; EXPRESSION; MUTATIONS; TUMORS; MEN;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PARP is a nuclear enzyme with a major function in the DNA damage response. PARP inhibitors (PARPi) have been developed for treating tumors harboring homologous recombination repair defects that lead to a dependency on PARP. There are currently three PARPi approved for use in advanced prostate cancer, and several others are in clinical trials for this disease. Recent clinical trial results have reported differential efficacy based on the specific PARPi utilized as well as patient race. There is a racial disparity in prostate cancer, in which African American males are twice as likely to develop and die from the disease compared with European American males. Despite the disparity, there continues to be a lack of diversity in clinical trial cohorts for prostate cancer. In this review, PARP nuclear functions, inhibition, and clinical relevance are explored through the lens of racial differences. This review will touch on the biological variations that have been explored thus far between African American and European American males with prostate cancer to offer a rationale for investigating PARPi response in the context of race at both basic science and clinical development levels.
引用
收藏
页码:2049 / 2059
页数:11
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