Food and Biodynamic Chemistry Laboratory, Graduate School of Agricultural Science, Tohoku University, Sendai 981-8555, Japan.
Biochem Biophys Res Commun. 2010 Jun 25;397(2):214-9. doi: 10.1016/j.bbrc.2010.05.087. Epub 2010 May 20.
Recent studies have demonstrated that tocotrienol (T3) is superior to tocopherol (Toc) for cancer chemoprevention. However, there is little information on whether Toc influences the anticancer property of T3. In this study, we investigated the influence of Toc on the cytotoxic effects of delta-T3 in DLD-1 human colorectal adenocarcinoma cells. Toc, especially alpha-Toc, attenuated delta-T3-induced cytotoxicity and apoptosis in DLD-1 cells, whereas Toc alone did not exhibit any cytotoxic effect. delta-T3-induced cell cycle arrest and proapoptotic gene/protein expression (e.g., p21, p27, and caspases) were abrogated by alpha-Toc. Furthermore, coadministration of alpha-Toc decreased delta-T3 uptake into DLD-1 cells in a dose-dependent manner. These results indicate that alpha-Toc is not only less cytotoxic to cancer cells, but it also reduces the cytotoxicity of delta-T3 by inhibiting its cellular uptake.
最近的研究表明,生育三烯酚(T3)在癌症化学预防方面优于生育酚(Toc)。然而,关于Toc 是否会影响 T3 的抗癌特性的信息很少。在这项研究中,我们研究了Toc 对 DLD-1 人结直肠腺癌细胞中 δ-T3 细胞毒性的影响。Toc,特别是 α-Toc,减弱了 δ-T3 诱导的 DLD-1 细胞的细胞毒性和细胞凋亡,而单独的 Toc 没有表现出任何细胞毒性作用。δ-T3 诱导的细胞周期停滞和促凋亡基因/蛋白表达(如 p21、p27 和半胱天冬酶)被 α-Toc 阻断。此外,α-Toc 的共给药以剂量依赖的方式降低了 DLD-1 细胞中 δ-T3 的摄取。这些结果表明,α-Toc 不仅对癌细胞的细胞毒性较小,而且通过抑制其细胞摄取来降低 δ-T3 的细胞毒性。