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Anti-proliferative and apoptotic activities of constituents of chloroform extract of Juglans regia leaves

机译:胡桃叶片氯仿提取物成分的抗增殖和凋亡活性

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Objectives: To evaluate anti-proliferative as well as apoptotic activities of compounds identified in chloroform extract of Juglans regia leaves, on human breast and oral cancer cell lines (MCF-7 and BHY). Materials and methods Column chromatography, MTT assay, flowcytometry and western blotting have all been used in the study. Results Bioassay-guided fractionation of chloroform extract of J. regia afforded isolation of 5-hydroxy-3,7,4′-trimethoxyflavone [1], lupeol [2], daucosterol [3], 4-hydroxy-α-tetralone [4], β-sitosterol [5], 5,7- dihydroxy-3,4′-dimethoxyflavone [6] and regiolone [7]. Structures of the compounds were established on the basis of spectroscopic analyses [Nuclear magnetic resonance (NMR) and mass]. All compounds inhibited proliferation of MCF-7 (human breast adenocarcinoma) and BHY (human oral squamous carcinoma) cells in a concentration-dependent manner. Compounds 6 and 7 had potent cytotoxic effects on both MCF-7 and BHY cells (IC50 21–51 μm), yet were not toxic to normal cells. MCF-7 growth inhibition was attributed to apoptosis; population of apoptotic cells increased from 1.12% in controls to 5.64 and 8.1% after 48-h treatment with compounds 6 and 7, indicating their potential at inducing early and late apoptosis. The caspase cascade was not activated, as indicated by only insignificant cleavage of caspase-3. Conclusions Our results suggest that compounds 6 and 7 can induce apoptosis in MCF-7 cells through the caspase-3 independent pathway.
机译:目的:评估在胡桃叶的氯仿提取物中鉴定出的化合物对人乳腺癌和口腔癌细胞系(MCF-7和BHY)的抗增殖和凋亡活性。材料和方法柱色谱,MTT测定,流式细胞术和蛋白质印迹均已用于研究。结果生物测定指导下的瑞格斯氯仿提取物的​​分馏提供了5-羟基-3,7,4'-三甲氧基黄酮的分离[1],羽扇豆酚[2],胡萝卜甾醇[3],4-羟基-α-四氢萘酮[4] ],β-谷固醇[5],5,7-二羟基-3,4'-二甲氧基黄酮[6]和区域内酮[7]。根据光谱分析[核磁共振(NMR)和质量]建立化合物的结构。所有化合物均以浓度依赖性方式抑制MCF-7(人乳腺腺癌)和BHY(人口腔鳞癌)细胞的增殖。化合物6和7对MCF-7和BHY细胞均具有有效的细胞毒性作用(IC50 21–51μm),但对正常细胞没有毒性。 MCF-7的生长抑制归因于细胞凋亡。化合物6和7处理48小时后,凋亡细胞的数量从对照组的1.12%增加到5.64和8.1%,表明它们具有诱导早期和晚期凋亡的潜力。半胱天冬酶级联没有被激活,如仅微不足道的半胱天冬酶3的裂解所表明的。结论我们的结果表明化合物6和7可以通过caspase-3独立途径诱导MCF-7细胞凋亡。

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