O'Shea M, Stanton C, Devery R
School of Biotechnology, Dublin City University, Ireland.
Anticancer Res. 1999 May-Jun;19(3A):1953-9.
The relationship between antioxidant-enzyme defence responses and cellular growth suppression in human MCF-7 (breast) and SW480 (colon) cancer cells, exposed to CLA in culture was studied. MCF-7 and SW480 cells (1 x 10(6)/flask) were cultured in appropriate medium for 4, 8 and 12 days with varying levels of CLA (0-30 ppm). A dose-dependent decrease in cell numbers and increase in lipid peroxidation, as determined by thiobarbituric acid reactive substances (TBARS) was observed in both cell lines following incubation with CLA. Exposure of both cell lines to 20 ppm CLA for 2-6 days produced a reduction (83-91%) in 3H-leucine incorporation into protein while 3H-uridine and 3H-thymidine incorporation into RNA and DNA were reduced by 49-91% and 86-98%, respectively, compared with untreated control cells. The activities of superoxide dismutase (SOD), catalase and glutathione peroxidase (GPx) were induced in both cell lines exposed to CLA (20 ppm) over a period of 12 days, although to a greater extent in MCF-7 cells than in SW480 cells. The data indicate that CLA-induced cytotoxicity against MCF-7 and SW480 cancer cell lines is related to the extent of lipid peroxidation of CLA treated cells and affirm that the CLA- induced antioxidant enzymes failed to protect these cells from cytotoxic lipid peroxidation products.
研究了在培养过程中暴露于共轭亚油酸(CLA)的人MCF - 7(乳腺)和SW480(结肠)癌细胞中抗氧化酶防御反应与细胞生长抑制之间的关系。将MCF - 7和SW480细胞(1×10⁶/瓶)在含有不同水平CLA(0 - 30 ppm)的合适培养基中培养4、8和12天。用硫代巴比妥酸反应性物质(TBARS)测定,在与CLA孵育后,两种细胞系均观察到细胞数量呈剂量依赖性减少以及脂质过氧化增加。两种细胞系暴露于20 ppm CLA 2 - 6天,与未处理的对照细胞相比,3H - 亮氨酸掺入蛋白质减少了83 - 91%,而3H - 尿苷和3H - 胸苷掺入RNA和DNA分别减少了49 - 91%和86 - 98%。在暴露于CLA(20 ppm)12天的两种细胞系中,超氧化物歧化酶(SOD)、过氧化氢酶和谷胱甘肽过氧化物酶(GPx)的活性均被诱导,尽管在MCF - 7细胞中的诱导程度大于SW480细胞。数据表明,CLA对MCF - 7和SW480癌细胞系的细胞毒性与CLA处理细胞的脂质过氧化程度有关,并证实CLA诱导的抗氧化酶未能保护这些细胞免受细胞毒性脂质过氧化产物的影响。