医学
肺癌
结直肠癌
癌症研究
细胞凋亡
细胞生长
癌症
细胞
不利影响
药理学
程序性细胞死亡
癌细胞
细胞周期
氯离子通道
赫尔格
治疗效果
内科学
肿瘤科
作者
Yohan Seo,Sion Lee,Raju Das,Sung Baek Jeong,Chul Soon Park,Minuk Kim,Daniel Yoon,Armin Sultana,KJ Maria Das,Jae-Eon Lee,Yong Hyun Jeon,Phan Thị Thanh Hương,Nguyễn Xuân Nhiệm,Joohan Woo
标识
DOI:10.3389/fphar.2025.1557193
摘要
Colorectal cancer (CRC) and non-small cell lung cancer (NSCLC) remain among the most challenging malignancies to treat due to therapy complexity, adverse events, and dose-limiting toxicities, which often result in treatment failure. NSCLC, in particular, has a high mortality rate attributed to late-stage diagnosis and therapeutic resistance. Anoctamin 1 (ANO1), a calcium-activated chloride channel, has been implicated in cancer progression and is an emerging therapeutic target. In this study, we identified vitexicarpin, a flavonoid isolated from Vitex trifolia, as a novel ANO1 inhibitor with anticancer potential. Vitexicarpin inhibited ANO1 channel function, reduced ANO1 protein levels, decreased cancer cell viability, and induced apoptosis in CRC and NSCLC cell lines. Importantly, vitexicarpin exhibited minimal hepatotoxicity and negligible hERG channel inhibition, supporting its safety profile. Collectively, our findings suggest that vitexicarpin is a promising candidate for the treatment of CRC and NSCLC through selective inhibition of ANO1.
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