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长叶刺蒺藜提取物诱导细胞凋亡。

Induction of apoptosis by Eurycoma longifolia jack extracts.

作者信息

Tee Thiam Tsui, Azimahtol Hawariah Lope Pihie

机构信息

School of Biosciences and Biotechnology, Faculty of Science and Technology, National University of Malaysia, 43600 UKM Bangi, Selangor, Malaysia.

出版信息

Anticancer Res. 2005 May-Jun;25(3B):2205-13.

PMID:16158965
Abstract

Extracts of the plant Eurycoma longifolia have been shown to possess cytotoxic, antimalarial, anti-ulcer, antipyretic and plant growth inhibition activities. The present study investigated the effects of extracts and their chromatographic fractions from the root of E. longifolia on the growth of a human breast cancer cell line, MCF-7. Our data indicated that E. longifolia extracts and fractions exert a direct antiproliferative activity on MCF-7. The bioassay-guided root fractionation resulted in the isolation of three active fractions, F5, F6 and F7, which displayed IC50 values of (6.17+/-0.38) microg/ml, (4.40+/-0.42) microg/ml and (20.00+/-0.08) microg/ml, respectively. The resultant from F7 purification, F16, exhibited a higher cytotoxic activity towards MCF-7, (IC50=15.23+/-0.66 microg/ml) and a certain degree of selectivity against a normal breast cell line, MCF-10A (IC50=66.31-0.47 microg/ml). F16 significantly increased apoptosis in MCF-7 cells, as evaluated by the Tdt-mediated dUTP nick end labelling assay and nuclear morphology. Western blotting revealed down-regulation of the anti-apoptotic Bcl-2 protein expression. F16, however, did not affect the expression of the pro-apoptotic protein, Bax. These results, therefore, suggest that F16 has antiproliferative effects on MCF-7 cells by inducing apoptosis through the modulation of Bcl-2 protein levels.

摘要

长叶刺蒺藜提取物已被证明具有细胞毒性、抗疟疾、抗溃疡、解热和植物生长抑制活性。本研究调查了长叶刺蒺藜根提取物及其色谱分离组分对人乳腺癌细胞系MCF-7生长的影响。我们的数据表明,长叶刺蒺藜提取物和组分对MCF-7具有直接的抗增殖活性。生物测定导向的根部分离得到了三个活性组分F5、F6和F7,其IC50值分别为(6.17±0.38)微克/毫升、(4.40±0.42)微克/毫升和(20.00±0.08)微克/毫升。F7纯化产物F16对MCF-7表现出更高的细胞毒性活性(IC50 = 15.23±0.66微克/毫升),并对正常乳腺细胞系MCF-10A具有一定程度的选择性(IC50 = 66.31 - 0.47微克/毫升)。通过TdT介导的dUTP缺口末端标记测定和核形态学评估,F16显著增加了MCF-7细胞中的凋亡。蛋白质印迹法显示抗凋亡蛋白Bcl-2的表达下调。然而,F16不影响促凋亡蛋白Bax的表达。因此,这些结果表明F16通过调节Bcl-2蛋白水平诱导凋亡,从而对MCF-7细胞具有抗增殖作用。

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