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Chemoprotection by sulforaphane: Keep one eye beyond Keap1

期刊

CANCER LETTERS
卷 233, 期 2, 页码 208-218

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2005.02.033

关键词

sulforaphane; chemoprevention

类别

资金

  1. NCI NIH HHS [CA90890, CA80176, P01 CA090890-05, R01 CA065525, R01 CA065525-08, R01 CA065525-09, CA66525, R01 CA080176, P01 CA090890, P01 CA090890-01A29001, R01 CA080176-05, P01 CA090890-01A20003] Funding Source: Medline
  2. NIEHS NIH HHS [P30 ES000210, P30 ES00210] Funding Source: Medline

向作者/读者索取更多资源

Sulforaphane (SFN) is an isothiocyanate found in cruciferous vegetables, with particularly high levels detected in broccoli and broccoli sprouts. Over a decade ago, this phytochemical was identified as a likely chemopreventive agent based on its ability to induce Phase 2 detoxification enzymes, as well as to inhibit Phase 1 enzymes involved in carcinogen activation. Considerable attention has focused on SFN as a 'blocking' agent, with the ability to modulate the Nrf2/Keap1 pathway, but recent evidence suggests that SFN acts by numerous other mechanisms. SFN induces cell cycle arrest and apoptosis in cancer cells, inhibits tubulin polymerization, activates checkpoint 2 kinase, and inhibits historic deacetylase activity. The latter findings suggest that SFN may be effective during the post-initiation stages of carcinogenesis, as a 'suppressing' agent. Moreover, pharmacological administration of SFN may be a promising therapeutic approach to the treatment of cancers, including those characterized by increased inflammation and involving viral or bacterial-related pathologies. The present review discusses the more widely established chemoprotective mechanisms of SFN, but makes the case for additional work on mechanisms that might be of importance during later stages of carcinogenesis, beyond Keap1. (c) 2005 Elsevier Ireland Ltd. All rights reserved.

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