Antiproliferative and apoptotic effects of tocopherols and tocotrienols on preneoplastic and neoplastic mouse mammary epithelial cells.

B S McIntyre, K P Briski, A Gapor, P W Sylvester
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引用次数: 154

Abstract

Studies were conducted to determine the comparative effects of tocopherols and tocotrienols on preneoplastic (CL-S1), neoplastic (-SA), and highly malignant (+SA) mouse mammary epithelial cell growth and viability in vitro. Over a 5-day culture period, treatment with 0-120 microM alpha- and gamma-tocopherol had no effect on cell proliferation, whereas growth was inhibited 50% (IC50) as compared with controls by treatment with the following: 13, 7, and 6 microM tocotrienol-rich-fraction of palm oil (TRF); 55, 47, and 23 microM delta-tocopherol; 12, 7, and 5 microM alpha-tocotrienol; 8, 5, and 4 microM gamma-tocotrienol; or 7, 4, and 3 microM delta-tocotrienol in CL-S1, -SA and +SA cells, respectively. Acute 24-hr exposure to 0-250 microM alpha- or gamma-tocopherol (CL-S1, -SA, and +SA) or 0-250 microM delta-tocopherol (CL-S1) had no effect on cell viability, whereas cell viability was reduced 50% (LD50) as compared with controls by treatment with 166 or 125 microM delta-tocopherol in -SA and +SA cells, respectively. Additional LD50 doses were determined as the following: 50, 43, and 38 microM TRF; 27, 28, and 23 microM alpha-tocotrienol; 19, 17, and 14 microM gamma-tocotrienol; or 16, 15, or 12 microM delta-tocotrienol in CL-S1, -SA, and +SA cells, respectively. Treatment-induced cell death resulted from activation of apoptosis, as indicated by DNA fragmentation. Results also showed that CL-S1, -SA, and +SA cells preferentially accumulate tocotrienols as compared with tocopherols, and this may partially explain why tocotrienols display greater biopotency than tocopherols. These data also showed that highly malignant +SA cells were the most sensitive, whereas the preneoplastic CL-S1 cells were the least sensitive to the antiproliferative and apoptotic effects of tocotrienols, and suggest that tocotrienols may have potential health benefits in preventing and/or reducing the risk of breast cancer in women.

生育酚和生育三烯醇对肿瘤前和肿瘤小鼠乳腺上皮细胞的抗增殖和凋亡作用。
研究确定了生育酚和生育三烯醇对肿瘤前(CL-S1)、肿瘤(-SA)和高度恶性(+SA)小鼠乳腺上皮细胞生长和体外活力的比较作用。在5天的培养期间,0-120微米α -和γ -生育酚处理对细胞增殖没有影响,而与对照相比,用以下处理抑制了50% (IC50): 13、7和6微米棕榈油富生育三烯醇部分(TRF);55、47和23微米的δ生育酚;12、7和5微米α -生育三烯醇;8、5和4微米γ -生育三烯醇;CL-S1、-SA和+SA细胞中的δ -生育三烯醇含量分别为7、4和3微米。急性暴露于0-250微米α -或γ -生育酚(CL-S1, -SA和+SA)或0-250微米δ生育酚(CL-S1) 24小时对细胞活力没有影响,而与对照组相比,在-SA和+SA细胞中分别使用166或125微米δ生育酚处理,细胞活力降低了50% (LD50)。额外LD50剂量确定如下:50、43和38微米TRF;27、28和23微米α -生育三烯醇;19、17和14微米γ -生育三烯醇;分别在CL-S1、-SA和+SA细胞中添加16、15或12微米的δ -生育三烯醇。DNA断裂表明,治疗诱导的细胞死亡是由细胞凋亡激活引起的。结果还表明,与生育酚相比,CL-S1、-SA和+SA细胞更倾向于积累生育三烯醇,这可能部分解释了为什么生育三烯醇比生育酚表现出更大的生物潜能。这些数据还表明,高度恶性的+SA细胞对生育三烯醇的抗增殖和凋亡作用最敏感,而肿瘤前的CL-S1细胞对生育三烯醇的抗增殖和凋亡作用最不敏感,这表明生育三烯醇可能在预防和/或降低女性乳腺癌风险方面具有潜在的健康益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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