ORIGINAL RESEARCH article
Front. Oncol.
Sec. Gastrointestinal Cancers: Colorectal Cancer
Volume 15 - 2025 | doi: 10.3389/fonc.2025.1644498
This article is part of the Research TopicInterdisciplinary Approaches for Uncovering the Anti-tumor Mechanisms of Chinese Drugs and Natural ProductsView all 6 articles
Artemisia absinthium L. ethanol extract inhibits the growth of gastrointestinal cancer cells by inducing apoptosis and mitochondria-dependent pathway
Provisionally accepted- 1People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, China
- 2Xinjiang University, Urumqi, China
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Objectives: Artemisia absinthium L. has a long history in the treatment of gastrointestinal cancer (GIC), but its molecular mechanisms remain unclear. Materials and methods: We identified and validated the active components and key targets in A. absinthium for the treatment of GIC by LC-MS and Network analysis. The antitumor effect of A. absinthium ethanol extract (AAEM-V) against gastrointestinal tract cancer in vitro and in vivo as well as the anticancer activity of the active ingredient, Luteolinidin, were further evaluated. Results: AAEM-V exhibited good anticancer activity in vitro and in vivo. The active ingredient Luteolinidin was taken to intersect with the targets of gastric and colorectal cancers, and 69 common targets were identified. A total of three core targets, SRC, EGFR, and AKT1, were screened according to PPI and molecularly docked with Luteolinidin, and it was found that their binding played a key role in the treatment of tumors. Meanwhile, its active ingredient Luteolinidin was found to induce ROS proliferation to promote apoptosis and prevent cells from entering S phase. Conclusion: These findings not only explored the anti-gastrointestinal cancer chemical properties of A. absinthium, but also provided a new research direction for the active ingredients and mechanism of action of traditional Chinese medicine.
Keywords: gastrointestinal cancer, Artemisia absinthium L., anti-tumor activity, Luteolinidin, Apoptosis
Received: 23 Jun 2025; Accepted: 15 Oct 2025.
Copyright: © 2025 Li, Yu, Ma, Li, Xia and Feng. 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:
Jinyao Li, ljyxju@xju.edu.cn
Lijie Xia, xlj@xju.edu.cn
Yan Feng, fengyan@xjrmyy.com
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.