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- Publisher Website: 10.1093/carcin/bgr261
- Scopus: eid_2-s2.0-84856582504
- PMID: 22095072
- WOS: WOS:000300039800001
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Article: Tocotrienol as a potential anticancer agent
Title | Tocotrienol as a potential anticancer agent | ||||
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Authors | |||||
Issue Date | 2012 | ||||
Publisher | Oxford University Press. The Journal's web site is located at http://carcin.oxfordjournals.org/ | ||||
Citation | Carcinogenesis, 2012, v. 33 n. 2, p. 233-239 How to Cite? | ||||
Abstract | Vitamin E is composed of two structurally similar compounds: tocopherols (TPs) and tocotrienols (T3). Despite being overshadowed by TP over the past few decades, T3 is now considered to be a promising anticancer agent due to its potent effects against a wide range of cancers. A growing body of evidence suggests that in addition to its antioxidative and pro-apoptotic functions, T3 possesses a number of anticancer properties that make it superior to TP. These include the inhibition of epithelial-to-mesenchymal transitions, the suppression of vascular endothelial growth factor tumor angiogenic pathway and the induction of antitumor immunity. More recently, T3, but not TP, has been shown to have chemosensitization and anti-cancer stem cell effects, further demonstrating the potential of T3 as an effective anticancer therapeutic agent. With most of the previous clinical studies on TP producing disappointing results, research has now focused on testing T3 as the next generation vitamin E for chemoprevention and cancer treatment. This review will summarize recent developments in the understanding of the anticancer effects of T3. We will also discuss current progress in clinical trials involving T3 as an adjuvant to conventional cancer therapy. © The Author 2011. Published by Oxford University Press. All rights reserved. | ||||
Persistent Identifier | http://hdl.handle.net/10722/149780 | ||||
ISSN | 2023 Impact Factor: 3.3 2023 SCImago Journal Rankings: 1.074 | ||||
ISI Accession Number ID |
Funding Information: QUT Vice Chancellor Fellowship (to M.T.L.). | ||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ling, MT | en_US |
dc.contributor.author | Luk, SU | en_US |
dc.contributor.author | AlEjeh, F | en_US |
dc.contributor.author | Khanna, KK | en_US |
dc.date.accessioned | 2012-06-26T05:58:29Z | - |
dc.date.available | 2012-06-26T05:58:29Z | - |
dc.date.issued | 2012 | en_US |
dc.identifier.citation | Carcinogenesis, 2012, v. 33 n. 2, p. 233-239 | en_US |
dc.identifier.issn | 0143-3334 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/149780 | - |
dc.description.abstract | Vitamin E is composed of two structurally similar compounds: tocopherols (TPs) and tocotrienols (T3). Despite being overshadowed by TP over the past few decades, T3 is now considered to be a promising anticancer agent due to its potent effects against a wide range of cancers. A growing body of evidence suggests that in addition to its antioxidative and pro-apoptotic functions, T3 possesses a number of anticancer properties that make it superior to TP. These include the inhibition of epithelial-to-mesenchymal transitions, the suppression of vascular endothelial growth factor tumor angiogenic pathway and the induction of antitumor immunity. More recently, T3, but not TP, has been shown to have chemosensitization and anti-cancer stem cell effects, further demonstrating the potential of T3 as an effective anticancer therapeutic agent. With most of the previous clinical studies on TP producing disappointing results, research has now focused on testing T3 as the next generation vitamin E for chemoprevention and cancer treatment. This review will summarize recent developments in the understanding of the anticancer effects of T3. We will also discuss current progress in clinical trials involving T3 as an adjuvant to conventional cancer therapy. © The Author 2011. Published by Oxford University Press. All rights reserved. | en_US |
dc.language | eng | en_US |
dc.publisher | Oxford University Press. The Journal's web site is located at http://carcin.oxfordjournals.org/ | en_US |
dc.relation.ispartof | Carcinogenesis | en_US |
dc.title | Tocotrienol as a potential anticancer agent | en_US |
dc.type | Article | en_US |
dc.identifier.email | Ling, MT:patling@hkucc.hku.hk | en_US |
dc.identifier.authority | Ling, MT=rp00449 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1093/carcin/bgr261 | en_US |
dc.identifier.pmid | 22095072 | - |
dc.identifier.scopus | eid_2-s2.0-84856582504 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-84856582504&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 33 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.spage | 233 | en_US |
dc.identifier.epage | 239 | en_US |
dc.identifier.isi | WOS:000300039800001 | - |
dc.publisher.place | United Kingdom | en_US |
dc.identifier.scopusauthorid | Ling, MT=7102229780 | en_US |
dc.identifier.scopusauthorid | Luk, SU=36981977600 | en_US |
dc.identifier.scopusauthorid | AlEjeh, F=6504391249 | en_US |
dc.identifier.scopusauthorid | Khanna, KK=35428143200 | en_US |
dc.identifier.issnl | 0143-3334 | - |