癌症研究
DNA损伤
癌症
卵巢癌
医学
聚ADP核糖聚合酶
合成致死
生物
免疫学
DNA修复
聚合酶
DNA
内科学
遗传学
作者
Sanjay de Mel,Ainsley Ryan Yan Bin Lee,Joelle Hwee Inn Tan,Rachel Tan,Limei Poon,Esther Hian Li Chan,Joanne Lee,Yen Lin Chee,Satish R. Lakshminarasappa,Patrick Jaynes,Anand D. Jeyasekharan
标识
DOI:10.3389/fonc.2024.1307839
摘要
Deregulation of the DNA damage response (DDR) plays a critical role in the pathogenesis and progression of many cancers. The dependency of certain cancers on DDR pathways has enabled exploitation of such through synthetically lethal relationships e.g., Poly ADP-Ribose Polymerase (PARP) inhibitors for BRCA deficient ovarian cancers. Though lagging behind that of solid cancers, DDR inhibitors (DDRi) are being clinically developed for haematological cancers. Furthermore, a high proliferative index characterize many such cancers, suggesting a rationale for combinatorial strategies targeting DDR and replicative stress. In this review, we summarize pre-clinical and clinical data on DDR inhibition in haematological malignancies and highlight distinct haematological cancer subtypes with activity of DDR agents as single agents or in combination with chemotherapeutics and targeted agents. We aim to provide a framework to guide the design of future clinical trials involving haematological cancers for this important class of drugs.
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