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谷胱甘肽和硫氧还蛋白抗氧化途径协同作用,推动癌症的发生和发展。

Glutathione and thioredoxin antioxidant pathways synergize to drive cancer initiation and progression.

机构信息

The Campbell Family Institute for Breast Cancer Research, University Health Network, 620 University Avenue, Toronto, ON M5G 2M9, Canada; Department of Medical Biophysics, University Health Network, 620 University Avenue, Toronto, ON M5G 2M9, Canada.

The Campbell Family Institute for Breast Cancer Research, University Health Network, 620 University Avenue, Toronto, ON M5G 2M9, Canada.

出版信息

Cancer Cell. 2015 Feb 9;27(2):211-22. doi: 10.1016/j.ccell.2014.11.019. Epub 2015 Jan 22.

Abstract

Controversy over the role of antioxidants in cancer has persisted for decades. Here, we demonstrate that synthesis of the antioxidant glutathione (GSH), driven by GCLM, is required for cancer initiation. Genetic loss of Gclm prevents a tumor's ability to drive malignant transformation. Intriguingly, these findings can be replicated using an inhibitor of GSH synthesis, but only if delivered prior to cancer onset, suggesting that at later stages of tumor progression GSH becomes dispensable potentially due to compensation from alternative antioxidant pathways. Remarkably, combined inhibition of GSH and thioredoxin antioxidant pathways leads to a synergistic cancer cell death in vitro and in vivo, demonstrating the importance of these two antioxidants to tumor progression and as potential targets for therapeutic intervention.

摘要

抗氧化剂在癌症中的作用一直存在争议,已经持续了几十年。在这里,我们证明了由 GCLM 驱动的抗氧化剂谷胱甘肽 (GSH) 的合成对于癌症的发生是必需的。Gclm 的遗传缺失会阻止肿瘤驱动恶性转化的能力。有趣的是,使用 GSH 合成抑制剂可以复制这些发现,但前提是在癌症发生之前使用,这表明在肿瘤进展的后期,GSH 变得可有可无,可能是由于来自替代抗氧化途径的补偿。值得注意的是,GSH 和硫氧还蛋白抗氧化途径的联合抑制导致体外和体内协同的癌细胞死亡,这表明这两种抗氧化剂对肿瘤进展很重要,并且可能成为治疗干预的潜在靶点。

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