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山核桃叶氯仿提取物成分的抗增殖和促凋亡活性。

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

机构信息

Department of Physiology and Pharmacology, Pasteur Institute of Iran, Tehran, 3159915111, Iran.

出版信息

Cell Prolif. 2014 Apr;47(2):172-9. doi: 10.1111/cpr.12090. Epub 2014 Jan 27.

Abstract

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.

摘要

目的

评估从核桃叶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)的抗增殖和促凋亡活性。

材料与方法

本研究采用柱层析、MTT 检测、流式细胞术和 Western blot 等方法。

结果

核桃叶氯仿提取物的生物活性导向分离得到了 5-羟基-3,7,4'-三甲氧基黄酮[1]、羽扇豆醇[2]、豆甾醇[3]、4-羟基-α-四氢萘酮[4]、β-谷甾醇[5]、5,7-二羟基-3,4'-二甲氧基黄酮[6]和 regiolone [7]。基于光谱分析[核磁共振(NMR)和质谱]确定了化合物的结构。所有化合物均以浓度依赖的方式抑制 MCF-7(人乳腺癌腺癌细胞)和 BHY(人口腔鳞状癌细胞)的增殖。化合物 6 和 7 对 MCF-7 和 BHY 细胞均具有较强的细胞毒性作用(IC50 为 21-51μm),但对正常细胞无毒性。MCF-7 生长抑制归因于细胞凋亡;与对照组相比,用化合物 6 和 7 处理 48 小时后,凋亡细胞的比例从 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。半胱天冬酶级联反应未被激活,表明 caspase-3 仅轻微裂解。

结论

我们的研究结果表明,化合物 6 和 7 可以通过 caspase-3 非依赖性途径诱导 MCF-7 细胞凋亡。

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