怀尔在增强铁蛋白自噬的同时,同时独立抑制抗氧化途径SLC7A11/GPX4,从而抑制肺癌。

IF 6.1 2区 生物学 Q1 CELL BIOLOGY
Xingxing Shi, Kun Liu, Yuchang Tian, Xinyi Bi, Junkai Zhang, Fengyi Ma, Wensheng Wei, Tongbiao Zhao
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引用次数: 0

摘要

槐儿(Trametes Robiniophila Murr)是一种传统的中药,已成为临床治疗癌症的一种有前景的药物,但其潜在的机制尚不清楚。在本研究中,我们证明怀尔通过诱导铁下垂有效地抑制肺癌。在机制上,淮儿通过ncoa4介导的FTH1铁蛋白自噬降解,同时独立下调肺癌细胞抗氧化途径SLC7A11/GPX4,提高细胞内铁水平。铁螯合剂去铁胺(DFO)和铁衰亡抑制剂铁抑素-1 (Fer-1)均可减轻淮洱诱导的细胞死亡。在脲烷诱导的肺肿瘤发生模型和细胞来源的异种移植(CDX)模型中,淮儿通过诱导铁上落显著抑制肿瘤进展,而SRS16-86可以抵消这一作用。我们的研究揭示了淮儿诱导铁下垂抑制肺癌的新机制,强调了其作为肺癌治疗剂或作为联合治疗策略的一部分的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Huaier suppresses lung cancer by simultaneously and independently inhibiting the antioxidant pathway SLC7A11/GPX4 while enhancing ferritinophagy.

Huaier (Trametes Robiniophila Murr), a traditional Chinese medicine, has emerged as a promising therapeutic agent against cancers in clinical settings, yet its underlying mechanisms remain elusive. In this study, we demonstrate that Huaier effectively suppresses lung cancer by inducing ferroptosis. Mechanistically, Huaier simultaneously and independently downregulates the antioxidant pathway SLC7A11/GPX4 and elevates intracellular iron levels through NCOA4-mediated ferritinophagy degradation of FTH1 in lung cancer cells. Both the iron chelator deferoxamine (DFO) and the ferroptosis inhibitor ferrostatin-1 (Fer-1) mitigate Huaier-induced cell death. In both urethane-induced lung tumorigenesis models and cell-derived xenograft (CDX) models, Huaier significantly inhibits tumor progression by inducing ferroptosis, which can be counteracted by SRS16-86. Our study uncovers a novel mechanism by which Huaier induces ferroptosis to suppress lung cancer, underscoring its potential as a therapeutic agent for lung cancer or as part of a combination therapy strategy.

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来源期刊
Cell Death Discovery
Cell Death Discovery Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
8.30
自引率
1.40%
发文量
468
审稿时长
9 weeks
期刊介绍: Cell Death Discovery is a multidisciplinary, international, online-only, open access journal, dedicated to publishing research at the intersection of medicine with biochemistry, pharmacology, immunology, cell biology and cell death, provided it is scientifically sound. The unrestricted access to research findings in Cell Death Discovery will foster a dynamic and highly productive dialogue between basic scientists and clinicians, as well as researchers in industry with a focus on cancer, neurobiology and inflammation research. As an official journal of the Cell Death Differentiation Association (ADMC), Cell Death Discovery will build upon the success of Cell Death & Differentiation and Cell Death & Disease in publishing important peer-reviewed original research, timely reviews and editorial commentary. Cell Death Discovery is committed to increasing the reproducibility of research. To this end, in conjunction with its sister journals Cell Death & Differentiation and Cell Death & Disease, Cell Death Discovery provides a unique forum for scientists as well as clinicians and members of the pharmaceutical and biotechnical industry. It is committed to the rapid publication of high quality original papers that relate to these subjects, together with topical, usually solicited, reviews, editorial correspondence and occasional commentaries on controversial and scientifically informative issues.
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