Literature DB >> 25620030

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

Isaac S Harris1, Aislinn E Treloar1, Satoshi Inoue2, Masato Sasaki3, Chiara Gorrini2, Kim Chung Lee4, Ka Yi Yung4, Dirk Brenner5, Christiane B Knobbe-Thomsen6, Maureen A Cox2, Andrew Elia2, Thorsten Berger2, David W Cescon1, Adewunmi Adeoye7, Anne Brüstle2, Sam D Molyneux8, Jacqueline M Mason2, Wanda Y Li2, Kazuo Yamamoto9, Andrew Wakeham2, Hal K Berman7, Rama Khokha8, Susan J Done7, Terrance J Kavanagh10, Ching-Wan Lam4, Tak W Mak11.   

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.
Copyright © 2015 Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 25620030     DOI: 10.1016/j.ccell.2014.11.019

Source DB:  PubMed          Journal:  Cancer Cell        ISSN: 1535-6108            Impact factor:   31.743


  304 in total

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