Joshi S S, Kuszynski C A, Benner E J, Bagchi M, Bagchi D
Department of Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha 68198-6395, USA.
Antioxid Redox Signal. 1999 Winter;1(4):563-70. doi: 10.1089/ars.1999.1.4-563.
Anticancer chemotherapeutic agents are effective in inhibiting growth of cancer cells in vitro and in vivo, however, toxicity to normal cells is a major problem. In this study, we assessed the effect of a novel IH636 grape seed proanthocyanidin extract (GSPE) to ameliorate chemotherapy-induced toxic effects in cultured Chang epithelial cells, established from nonmalignant human tissue. These cells were treated in vitro with idarubicin (Ida) (30 nM) or 4-hydroxyperoxycyclophosphamide (4HC) (1 microg/ml) with or without GSPE (25 microg/ml). The cells were grown in vitro and the growth rate of the cells was determined using the MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; thiazolyl blue] assay. Our results showed that GSPE decreased the growth inhibitory and cytotoxic effects of Ida as well as 4HC on Chang epithelial cells in vitro. Because these chemotherapeutic agents are known to induce apoptosis in the target cells, we analyzed the Chang epithelial cells for apoptotic cell population by flow cytometry. There was a significant decrease in the number of cells undergoing apoptosis following treatment with GSPE. We also found increased expression of the anti-apoptotic protein Bcl-2 in GSPE-treated cells using western blot techniques. Thus, these results indicate that GSPE can be a potential candidate to ameliorate the toxic effects associated with chemotherapeutic agents and one of the mechanisms of action of GSPE includes upregulation of Bcl-2 expression.
抗癌化疗药物在体外和体内均能有效抑制癌细胞生长,然而,对正常细胞的毒性是一个主要问题。在本研究中,我们评估了一种新型的IH636葡萄籽原花青素提取物(GSPE)对减轻化疗诱导的非恶性人体组织来源的培养Chang上皮细胞毒性作用的效果。这些细胞在体外分别用伊达比星(Ida)(30 nM)或4-羟基过氧环磷酰胺(4HC)(1微克/毫升)处理,同时或不同时添加GSPE(25微克/毫升)。细胞在体外培养,使用MTT [3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐;噻唑蓝] 法测定细胞生长速率。我们的结果表明,GSPE在体外降低了Ida以及4HC对Chang上皮细胞的生长抑制和细胞毒性作用。由于已知这些化疗药物可诱导靶细胞凋亡,我们通过流式细胞术分析Chang上皮细胞的凋亡细胞群体。用GSPE处理后,凋亡细胞数量显著减少。我们还使用蛋白质印迹技术发现,GSPE处理的细胞中抗凋亡蛋白Bcl-2的表达增加。因此,这些结果表明,GSPE可能是减轻与化疗药物相关毒性作用的潜在候选物,GSPE的作用机制之一包括上调Bcl-2表达。