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新型化合物蓝萼甲素H的体内外抗肝癌活性

Anti-hepatoma activity of a novel compound glaucocalyxin H in vivo and in vitro.

作者信息

Hai Guangfan, Zhang Chong, Jia Yanlong, Bai Suping, Han Jinfen, Guo Lanqing, Cui Taizhen, Niu Bingxuan, Huang Feng, Song Yu

机构信息

School of Pharmacy, Xinxiang Medical University, Jinsui Avenue 601, Xinxiang, 453003, Henan, China.

出版信息

AAPS PharmSciTech. 2015 Jun;16(3):496-504. doi: 10.1208/s12249-014-0227-3. Epub 2014 Nov 6.

Abstract

Glaucocalyxin H (GLH) is a new compound isolated from a traditional Chinese medical herb Isodon japonica var. glaucocalyx which has been used for folk medicine. This study was carried out for the first time to investigate the potential role of GLH in anti-hepatoma activity and underlying mechanisms in it. GLH could inhibit the growth of tumor in mice and induce HepG2 cells to death as assessed by the tumor reduction assay, toxic assay, morphological change, and survival rate assay. Many antitumor drugs originated from plants could inhibit the growth of tumor by inducing cells to apoptosis. The morphological changes of HepG2 cells treated with different concentrations of GLH under fluorescence and electron microscope and apoptotic rates were detected to verify its effect on apoptosis. As shown in the study, GLH could induce HepG2 cells to apoptosis in a dose-dependent manner. Bcl2 and Bax proteins played important roles in apoptosis and the disequilibrium between Bcl2 and Bax might result in apoptosis. The expression of Bax protein was upregulated and Bcl2 protein was downregulated in HepG2 cells treated with GLH assessed by Western blotting, and they were in a dose-dependent manner. Taken together, GLH can inhibit the growth of hepatoma cells in vivo and in vitro by inducing cell apoptosis due to the decreased Bcl2 and increased Bax proteins suggesting that GLH could be a potential candidate as an anti-hepatoma agent for the therapeutic treatment of hepatoma.

摘要

蓝萼甲素(GLH)是从传统中药毛叶香茶菜中分离出的一种新化合物,该植物已被用于民间医学。本研究首次对GLH在抗肝癌活性中的潜在作用及其潜在机制进行了研究。通过肿瘤缩小试验、毒性试验、形态学变化和存活率试验评估,GLH可抑制小鼠肿瘤生长并诱导HepG2细胞死亡。许多源自植物的抗肿瘤药物可通过诱导细胞凋亡来抑制肿瘤生长。检测不同浓度GLH处理的HepG2细胞在荧光和电子显微镜下的形态变化及凋亡率,以验证其对凋亡的影响。研究表明,GLH可呈剂量依赖性地诱导HepG2细胞凋亡。Bcl2和Bax蛋白在凋亡中起重要作用,Bcl2和Bax之间的失衡可能导致凋亡。通过蛋白质免疫印迹法评估,在GLH处理的HepG2细胞中,Bax蛋白表达上调,Bcl2蛋白表达下调,且呈剂量依赖性。综上所述,GLH可通过诱导细胞凋亡抑制体内外肝癌细胞生长,这是由于Bcl2减少和Bax增加所致,表明GLH可能是一种潜在的抗肝癌治疗药物候选物。

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Anti-hepatoma activity of a novel compound glaucocalyxin H in vivo and in vitro.新型化合物蓝萼甲素H的体内外抗肝癌活性
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