ORIGINAL RESEARCH article
Front. Pharmacol.
Sec. Experimental Pharmacology and Drug Discovery
Volume 16 - 2025 | doi: 10.3389/fphar.2025.1557193
This article is part of the Research TopicInsights in Experimental Pharmacology and Drug Discovery: 2024View all 13 articles
Vitexicarpin demonstrates anticancer potential by inhibiting anoctamin 1 in colorectal and non-small cell lung cancers
Provisionally accepted- 1Korea Bio Polytechnic University, Nonsan, South Chungcheong, Republic of Korea
- 2Daegu-Gyeongbuk Medical Innovation Foundation (DGMIF), Daegu, Daegu, Republic of Korea
- 3College of Medicine, Dongguk University, Gyeongju, North Gyeongsang, Republic of Korea
- 4Vietnam Academy of Science and Technology, Hanoi, Vietnam
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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 doselimiting 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.
Keywords: ANO1, Vitexicarpin, colorectal cancer, Non-small cell lung cancer, Apoptosis
Received: 08 Jan 2025; Accepted: 06 May 2025.
Copyright: © 2025 Seo, Lee, Jeong, Kim, Yoon, Das, Sultana, Das, Lee, Jeon, Phan, Nhiem, Woo and Park. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Yohan Seo, Korea Bio Polytechnic University, Nonsan, 320-905, South Chungcheong, Republic of Korea
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