Wada Sayori, Satomi Yoshiko, Murakoshi Michiaki, Noguchi Noriko, Yoshikawa Toshikazu, Nishino Hoyoku
Department of Biochemistry and Molecular Biology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kawaramachi Hirokoji, Kamigyo-ku, Kyoto 602-0841, Japan.
Cancer Lett. 2005 Nov 18;229(2):181-91. doi: 10.1016/j.canlet.2005.06.036. Epub 2005 Aug 10.
Tocotrienols have been reported to have higher biological activities than tocopherols. We investigated the antitumor effect of tocotrienols both in vivo and in vitro. Oral administration of tocotrienols resulted in significant suppression of liver and lung carcinogenesis in mice. In human hepatocellular carcinoma HepG2 cells, delta-tocotrienol exerted more significant antiproliferative effect than alpha-, beta-, and gamma-tocotrienols. delta-Tocotrienol induced apoptosis, and also tended to induce S phase arrest. On the other hand, gene expression analysis showed that delta-tocotrienol increased CYP1A1 gene, a phase I enzyme. Although further study will be necessary to investigate possible adverse effect, the data obtained in present study suggest that tocotrienols could be promising agents for cancer prevention.
据报道,生育三烯酚比生育酚具有更高的生物活性。我们在体内和体外研究了生育三烯酚的抗肿瘤作用。口服生育三烯酚可显著抑制小鼠肝脏和肺部的致癌作用。在人肝癌HepG2细胞中,δ-生育三烯酚比α-、β-和γ-生育三烯酚具有更显著的抗增殖作用。δ-生育三烯酚诱导细胞凋亡,并且还倾向于诱导S期停滞。另一方面,基因表达分析表明,δ-生育三烯酚增加了I相酶CYP1A1基因的表达。尽管需要进一步研究以调查可能的不良反应,但本研究获得的数据表明,生育三烯酚可能是有前景的癌症预防药物。