杀伤力
合成致死
倍性
驱动蛋白
生物
微管
基因
遗传学
DNA修复
作者
Qingsong Chen,Xiangyang Le,Li Qianbin,Suyou Liu,Zhuo Chen
标识
DOI:10.1016/j.drudis.2024.104142
摘要
Currently, various antimitotic inhibitors applied in tumor therapy. However, these inhibitors exhibit targeted toxicity to some extent. As a motor protein, kinesin family member 18A (KIF18A) is crucial to spindle formation and is associated with tumors exhibiting characteristics such as chromosomal aneuploidy, whole-genome doubling, and chromosomal instability. Differing from traditional antimitotic targets, KIF18A exhibits tumor-specific selectivity. The functional loss or attenuation of KIF18A results in vulnerability of tumor cells with ploidy-specific characteristics, with lesser effects on diploid cells. Research on inhibitors targeting KIF18A with ploidy-specific lethality holds significant importance. This review provides a brief overview of the regulatory mechanisms of the ploidy-specific lethality target KIF18A and the research advancements in its inhibitors, aiming to facilitate the development of KIF18A inhibitors.
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