免疫疗法
癌症研究
肿瘤微环境
聚ADP核糖聚合酶
医学
免疫检查点
PARP抑制剂
PD-L1
癌症免疫疗法
癌症
免疫系统
免疫学
生物
聚合酶
DNA
内科学
遗传学
作者
Qi Liu,Chunmei Zhang,Yixuan Gao,Dongmei Feng,Dawei Deng,Yun Pan
标识
DOI:10.1002/adbi.202400720
摘要
Abstract Deficiencies in DNA damage repair (DDR), such as poly (ADP‐ribose) polymerase (PARP) deficient, cause cancer development by promoting DNA mutations while also exposing the specificity and vulnerability of cancer to afford a treatment option. PARP inhibitor (PARPi) has shown great prospects in the treatment of tumors carrying homologous recombination (HR) deficiencies, such as germline BRCA1/2 mutations. PARPi leads to an increase in the expression of tumor neoantigen, interferon (IFN), and programmed cell death 1/programmed death‐ligand 1 (PD‐1/PD‐L1), which also regulate the tumor microenvironment (TME), promoting a deeper anti‐tumor immunotherapy. ICIs targeting PD‐1/PD‐L1 and cytotoxic T‐lymphocyte‐associated protein 4 (CTLA‐4) have achieved impressive success in the treatment of malignancies. Considering PARPi do enhance the anti‐tumor response of ICIs, the combination of PARPi and ICIs has gradually become an alternative treatment option for individuals not receiving apparent efficacy from ICI monotherapy. In this review, the emphasis will be on the mechanisms and immune responses associated with PARPi, profess the principle, then count the clinical studies of this combination therapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI