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- Publisher Website: 10.1016/j.ccell.2014.11.019
- Scopus: eid_2-s2.0-84922783167
- PMID: 25620030
- WOS: WOS:000349515200009
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Article: Glutathione and Thioredoxin Antioxidant Pathways Synergize to Drive Cancer Initiation and Progression
Title | Glutathione and Thioredoxin Antioxidant Pathways Synergize to Drive Cancer Initiation and Progression |
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Authors | |
Issue Date | 2015 |
Publisher | Cell Press. The Journal's web site is located at http://www.elsevier.com/locate/ccell |
Citation | Cancer Cell, 2015, v. 27 n. 2, p. 211-222 How to Cite? |
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. |
Persistent Identifier | http://hdl.handle.net/10722/212130 |
ISSN | 2023 Impact Factor: 48.8 2023 SCImago Journal Rankings: 17.507 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Harris, IS | - |
dc.contributor.author | Treloar, AE | - |
dc.contributor.author | Inoue, S | - |
dc.contributor.author | Sasaki, M | - |
dc.contributor.author | Gorrini, C | - |
dc.contributor.author | Lee, KC | - |
dc.contributor.author | Yung, KY | - |
dc.contributor.author | Brenner, D | - |
dc.contributor.author | Knobbe-Thomsen, CB | - |
dc.contributor.author | Cox, MA | - |
dc.contributor.author | Elia, A | - |
dc.contributor.author | Berger, T | - |
dc.contributor.author | Cescon, DW | - |
dc.contributor.author | Adeoye, A | - |
dc.contributor.author | Brüstle, A | - |
dc.contributor.author | Molyneux, SD | - |
dc.contributor.author | Mason, JM | - |
dc.contributor.author | Li, WY | - |
dc.contributor.author | Yamamoto, K | - |
dc.contributor.author | Wakeham, A | - |
dc.contributor.author | Berman, HK | - |
dc.contributor.author | Khokha, R | - |
dc.contributor.author | Done, SJ | - |
dc.contributor.author | Kavanagh, TJ | - |
dc.contributor.author | Lam, CW | - |
dc.contributor.author | Mak, TW | - |
dc.date.accessioned | 2015-07-21T02:24:07Z | - |
dc.date.available | 2015-07-21T02:24:07Z | - |
dc.date.issued | 2015 | - |
dc.identifier.citation | Cancer Cell, 2015, v. 27 n. 2, p. 211-222 | - |
dc.identifier.issn | 1535-6108 | - |
dc.identifier.uri | http://hdl.handle.net/10722/212130 | - |
dc.description.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. | - |
dc.language | eng | - |
dc.publisher | Cell Press. The Journal's web site is located at http://www.elsevier.com/locate/ccell | - |
dc.relation.ispartof | Cancer Cell | - |
dc.title | Glutathione and Thioredoxin Antioxidant Pathways Synergize to Drive Cancer Initiation and Progression | - |
dc.type | Article | - |
dc.identifier.email | Lee, KC: lee1983@hku.hk | - |
dc.identifier.email | Lam, CW: ching-wanlam@pathology.hku.hk | - |
dc.identifier.email | Mak, TW: tmak@uhnres.utoronto.ca | - |
dc.identifier.authority | Lam, CW=rp00260 | - |
dc.identifier.authority | Mak, TW=rp02746 | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1016/j.ccell.2014.11.019 | - |
dc.identifier.pmid | 25620030 | - |
dc.identifier.scopus | eid_2-s2.0-84922783167 | - |
dc.identifier.hkuros | 245380 | - |
dc.identifier.volume | 27 | - |
dc.identifier.issue | 2 | - |
dc.identifier.spage | 211 | - |
dc.identifier.epage | 222 | - |
dc.identifier.isi | WOS:000349515200009 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 1535-6108 | - |