Department of Pharmacology, Toxicology and Therapeutics, School of Medicine, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Eur J Cancer. 2010 Jul;46(10):1882-91. doi: 10.1016/j.ejca.2010.02.004. Epub 2010 Mar 10.
It was reported recently that resveratrol could sensitise a number of cancer cell lines to the anticancer actions of several other cancer drugs, including paclitaxel. In the present study, we further investigated whether resveratrol could sensitise human breast cancer cells to paclitaxel-induced cell death. Unexpectedly, we found that resveratrol strongly diminished the susceptibility of MDA-MB-435s, MDA-MB-231 and SKBR-3 cells to paclitaxel-induced cell death in culture, although this effect was not observed in MCF-7 cells. Using MDA-MB-435s cells as a representative model, a similar observation was made in athymic nude mice. Mechanistically, the modulating effect of resveratrol was partially attributable to its inhibition of paclitaxel-induced G(2)/M cell cycle arrest, together with an accumulation of cells in the S-phase. In addition, resveratrol could suppress paclitaxel-induced accumulation of reactive oxygen species (ROS) and subsequently the inactivation of anti-apoptotic Bcl-2 family proteins. These observations suggest that the strategy of concomitant use of resveratrol with paclitaxel is detrimental in certain types of human cancers. Given the widespread use of resveratrol among cancer patients, this study calls for more preclinical and clinical testing of the potential benefits and harms of using resveratrol as a dietary adjuvant in cancer patients.
最近有报道称,白藜芦醇可以使多种癌细胞系对包括紫杉醇在内的几种其他抗癌药物的抗癌作用更加敏感。在本研究中,我们进一步研究了白藜芦醇是否可以使人类乳腺癌细胞对紫杉醇诱导的细胞死亡更加敏感。出乎意料的是,我们发现白藜芦醇强烈降低了 MDA-MB-435s、MDA-MB-231 和 SKBR-3 细胞对紫杉醇诱导的细胞死亡的敏感性,尽管在 MCF-7 细胞中未观察到这种作用。使用 MDA-MB-435s 细胞作为代表性模型,在无胸腺裸鼠中也观察到了类似的现象。从机制上讲,白藜芦醇的调节作用部分归因于其抑制紫杉醇诱导的 G2/M 细胞周期阻滞,以及 S 期细胞的积累。此外,白藜芦醇可以抑制紫杉醇诱导的活性氧(ROS)的积累,从而使抗凋亡 Bcl-2 家族蛋白失活。这些观察结果表明,在某些类型的人类癌症中,同时使用白藜芦醇和紫杉醇的策略是有害的。鉴于癌症患者广泛使用白藜芦醇,本研究呼吁对将白藜芦醇作为癌症患者饮食辅助剂的潜在益处和危害进行更多的临床前和临床测试。