顺铂
癌症干细胞
化学
癌细胞
前药
细胞毒性
A549电池
细胞凋亡
癌症
药理学
癌症研究
肺癌
体内
干细胞
细胞生物学
体外
生物化学
生物
化疗
内科学
医学
生物技术
作者
Xinyi Wang,Zhikun Liu,Yuanjiang Wang,Shaohua Gou
标识
DOI:10.1021/acs.jmedchem.2c00472
摘要
Acquired resistance remains a major barrier for the treatment of non-small cell lung cancer, while cancer stem cells (CSCs) usually lead to the occurrence of drug resistance. We herein report a series of platinum(IV) prodrugs containing CSCs-inhibitory species derived from a known CSCs inhibitor BBI608 in the axial position. Among them, complex 15 exerted the most potent cytotoxicity against A549 and A549/CDDP cancer cells. Besides, 15 could suppress cancer cell stemness, superior to BBI608, and overcome cisplatin resistance. Following assays indicated that an enhanced intracellular accumulation of 15 effectively triggered DNA damage, induced ROS generation, activated mitochondrial apoptosis pathway, and suppressed cell motility via p53 pathway in A549/CDDP cells. In vivo tests indicated that 15 exhibited potent antitumor effects without causing loss in the body weight. Our study provides a novel and efficient approach to promote the antitumor activity of platinum-based prodrugs and overcome cisplatin resistance via inhibiting cancer cell stemness.
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