合成致死
药物发现
癌症
癌细胞
癌变
药品
生物
癌症研究
计算生物学
药理学
生物信息学
DNA修复
生物化学
遗传学
基因
作者
Zekun Zeng,Wenfang Zheng,Peng Hou
标识
DOI:10.1016/j.pharmthera.2022.108219
摘要
Drug-metabolizing enzymes (DMEs) have shown increasing importance in anticancer therapy. It is not only due to their effect on activation or deactivation of anticancer drugs, but also because of their extensive connections with pathological and biochemistry changes during tumorigenesis. Meanwhile, it has become more accessible to discovery anticancer drugs that selectively targeted cancer cells with the development of synthetic lethal screen technology. Synthetic lethal strategy makes use of unique genetic markers that different cancer cells from normal tissues to discovery anticancer agents. Dysregulation of DMEs has been found in various cancers, making them promising candidates for synthetic lethal strategy. In this review, we will systematically discuss about the role of DMEs in tumor progression, the application of synthetic lethality strategy in drug discovery, and a link between DMEs and synthetic lethal of cancer.
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