Poly (ADP-Ribose) Polymerases (PARPs) and PARP Inhibitor-Targeted Therapeutics

被引:11
作者
Li, Nan [1 ]
Wang, Yifan [1 ,2 ]
Deng, Weiye [3 ]
Lin, Steven H. [1 ,3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Expt Radiat Oncol, Houston, TX 77030 USA
[2] Univ Texas Houston, Grad Sch Biomed Sci, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
PARP inhibitors; BRCA mutation; synthetic lethal; Tankyrase inhibitors; poly-ADP-ribose polymerase 1; ovarian cancers; POLY(ADP-RIBOSE) POLYMERASE; DNA-DAMAGE; STRUCTURAL BASIS; OPEN-LABEL; TANKYRASE; RIBOSYLATION; MAINTENANCE; CHECKPOINT; DOMAINS; BRCA2;
D O I
10.2174/1871520618666181109164645
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Poly-ADP-ribosylation, that is, adding ADP-ribose moieties to a protein, is a unique type of protein post-translational modification that regulates various cellular processes such as DNA repair. mitosis, transcription, and cell growth. Small-molecule inhibitors of poly-ADP-ribose polymerase 1 (PARP1) have been developed as anticancer agents because inhibition of PARP enzymes may be a synthetic lethal strategy for cancers with or BRCA2 mutations. However, there are still questions surrounding PARP inhibitors Methods/Results: Data were collected from Pubmed. Medline, through searching of these keywords: "PARP", "BRCA", "Synthetic lethal" and "Tankyrase inhibitors". We describe the current knowledge of PARP inhibition and its effects on DNA damage; mechanisms of resistance to PARP inhibitors; the evolution of PARP inhibitors; and the potential use of PARP5a/b (tankyrases) inhibitors in cancer treatment. Conclusion: PARP inhibitors are already showing promise as therapeutic tools, especially in the management of BRCA-mutated breast and ovarian cancers but also in tumors with dysfunctional BRCA genes. Small-molecule tankyrase inhibitors are important for increasing our understanding of tankyrase biology.
引用
收藏
页码:206 / 212
页数:7
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