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    Review

    Targeting Intrinsic and Extrinsic Pathways of Ferroptosis: A Novel Anticancer Strategy of Curcumin

    Wei Hao1, Yuan Gao1, Bangwei Cao1 Corresponding author

    1. 1Cancer Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China

    CORRESPONDENCE

    Bangwei Cao

    Cancer Center, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China.

    caobangwei@ccmu.edu.cn

    Received: 05-02-2024; Accepted: 08-04-2024.

    Volume 20, Issue 4 · pp. 1061–1070 · PUBLISHED 2024 · DOI: 10.1177/09731296241251957

    View on Pharmacogn. Mag. original site ↗

    ABSTRACT

    Background: The turmeric rhizome yields a medicinal compound called curcumin. Curcumin’s anticancer methods mostly involve blocking cell invasion and proliferation, controlling gene expression, preventing angiogenesis, triggering apoptosis, and inducing ferroptosis. A brand-new nonapoptotic kind of planned cell death is called ferroptosis. Ferroptosis can be initiated through two major pathways: the extrinsic or transporter-dependent pathway, and the intrinsic or enzyme-regulated pathway. It is unknown, therefore, how curcumin and its derivatives prevent cancer by controlling ferroptosis. Purpose: Through this review, we concentrate on the possible anticancer mechanisms of curcumin by means of its effect on ferroptosis; the regulation of iron metabolism, the synthesis of reactive oxygen species, and the targeting of antioxidant pathways represent a few of these processes. Methodology: Retrieve English literature of curcumin and its derivatives in the treatment of tumor by ferroptosis from databases such as Web of Science, etc. Conclusion: This review provides a rationale for the clinical use of curcumin and its derivatives as anticancer agents.

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      Hao, W., Gao, Y., & Cao, B. (2024). Targeting Intrinsic and Extrinsic Pathways of Ferroptosis: A Novel Anticancer Strategy of Curcumin. Pharmacognosy Magazine, 20(4), 1061–1070. https://doi.org/10.1177/09731296241251957