Recent Progress in Poly(ADP-Ribose) Polymerase-1 Inhibitors for Application in Cancer

被引:0
作者
Mehra, Anuradha [1 ]
Islam, Shahnaz [1 ]
Sangwan, Rekha [1 ]
机构
[1] Lovely Profess Univ, Sch Pharmaceut Sci, Dept Pharmaceut Chem, Jalandhar Delhi GT Rd NH 1, Phagwara 144411, Punjab, India
关键词
Base excision repair; Biomarkers; BRCA mutations; Clinical trials; Combination therapy; DNA damage; <italic>IC</italic>50 value; PARP inhibition; Resistance mechanism; Synthetic lethality; Toxicity and side effects; Tumor selectivity; DNA-REPAIR; SYNTHETIC LETHALITY; ADP-RIBOSYLATION; FUNCTIONAL-ASPECTS; DUAL INHIBITORS; PARP INHIBITORS; BREAST-CANCER; BRCA; DERIVATIVES; DISCOVERY;
D O I
10.1002/slct.202404277
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An ADP-ribosylating enzyme called poly (ADP-ribose) polymerase 1 (PARP1) is necessary to start several types of DNA repair. PARP1 also contributes significantly to the regulation of gene expression through enzyme-independent motif recognition and enzyme-dependent chromatin remodeling. Thus, synthetic lethality is achieved in the therapy of tumors and cancers by blocking undesired DNA repair by the inhibition of its enzyme activity with small molecules. In addition to outlining the most recent research from 2019 to 2024 on the precise ways in which PARP1 regulates each process independently, we discussed how transcription and DNA repair are interdependent enough that perturbations caused by PARP1 enzymatic inhibition, disease-related enzyme hyperactivation. Herein, this concept review systematically summarizes the different approach for designing selective PARP1 inhibitor that are i) PARP1-DNA trapping approach, ii) hybrid approach, iii) PROTAC approach, and iv) dual target inhibitor approach and updates on clinical trials.
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