化学
奥拉帕尼
DNA损伤修复
软膜
DNA修复
合成致死
药理学
癌症
聚ADP核糖聚合酶
计算生物学
癌症研究
生物
DNA
生物化学
遗传学
聚合酶
作者
Yinghan Wang,Jingtao Zhang,Xiaochen Wu,Longjiang Huang,Wen‐Jing Xiao,Chuanlong Guo
标识
DOI:10.1021/acs.jmedchem.4c02642
摘要
PARP (poly-ADP ribose polymerase) has received widespread attention in cancer treatment. Research has shown that PARP plays a crucial role in DNA damage repair and has become a popular target for drug design. Based on the mechanism of "synthetic lethality", multiple PARPis (PARP inhibitors) have been launched for the treatment of BRCA deficient tumors. For example, the approved PARPis have shown significant potential in cancer treatment, particularly in breast cancer and cancers associated with BRCA1/BRCA2 deficiencies. However, the clinical efficacy and safety of PARP inhibitors in different cancers remain issues that cannot be overlooked. The design of PARPis aims to eliminate their resistance and broaden their application scope. Designing selective PARP-1 inhibitors is also a potential strategy. PROTACs (Proteolysis Targeting Chimeras) to degrade PARP have become a potential novel cancer treatment strategy.
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