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Abstract Title:

Sesamin synergistically potentiates the anticancer effects ofγ-tocotrienol in mammary cancer cell lines.

Abstract Source:

Fitoterapia. 2013 Jan ;84:347-59. Epub 2012 Dec 22. PMID: 23266736

Abstract Author(s):

Mohamed R Akl, Nehad M Ayoub, Bilal S Abuasal, Amal Kaddoumi, Paul W Sylvester

Article Affiliation:

Mohamed R Akl

Abstract:

γ-Tocotrienol and sesamin are phytochemicals that display potent anticancer activity. Since sesamin inhibits the metabolic degradation of tocotrienols, studies were conducted to determine if combined treatment with sesamin potentiates the antiproliferative effects of γ-tocotrienol on neoplastic mouse (+SA) and human (MCF-7 and MDA-MB-231) mammary cancer cells. Results showed that treatment with γ-tocotrienol or sesamin alone induced a significant dose-responsive growth inhibition, whereas combination treatment with these agents synergistically inhibited the growth of +SA, MCF-7 and MDA-MB-231 mammary cancer cells, while similar treatment doses were found to have little or no effect on normal (mouse CL-S1 and human MCF-10A) mammary epithelial cell growth or viability. However, sesamin synergistic enhancement of γ-tocotrienol-induced anticancer effects was not found to be mediated froma reduction in γ-tocotrienol metabolism. Rather, combined treatment with subeffective doses of γ-tocotrienol and sesamin was found to induce G1 cell cycle arrest, and a corresponding decrease in cyclin D1, CDK2, CDK4, CDK6, phospho-Rb, and E2F1 levels, and increase in p27 and p16 levels. Additional studies showed that the antiproliferative effect of combination treatment did not initiate apoptosis or result in a decrease in mammary cancer cell viability. Taken together, these findings indicate that the synergistic antiproliferative action of combined γ-tocotrienol and sesamin treatment inmouse and human mammary cancer cells is cytostatic, not cytotoxic, and results from G1 cell cycle arrest.

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Sayer Ji
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