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去镁叶绿素a,半枝莲中的一种活性成分,可逆转人肝癌细胞系R-HepG2中P-糖蛋白介导的多药耐药性。

Pheophorbide a, an active component in Scutellaria barbata, reverses P-glycoprotein-mediated multidrug resistance on a human hepatoma cell line R-HepG2.

作者信息

Tang Patrick Ming-Kuen, Chan Judy Yuet-Wa, Zhang Dong-Mei, Au Shannon Wing-Ngor, Fong Wing-Ping, Kong Siu-Kai, Tsui Stephen Kwok-Wing, Waye Mary Mui-Yee, Mak Thomas Chung-Wai, Fung Kwok-Pui

机构信息

Department of Biochemistry, The Chinese University of Hong Kong, Shatin, Hong Kong, China.

出版信息

Cancer Biol Ther. 2007 Apr;6(4):504-9. doi: 10.4161/cbt.6.4.3814.

DOI:10.4161/cbt.6.4.3814
PMID:17457045
Abstract

Scutellaria barbata, a Traditional Chinese Medicine native in southern China, has been widely used for treating liver diseases. In this study, the anti-proliferative effect of Pheophorbide a (Pa), an active component from S. barbata, was examined on a multi-drug resistant (MDR) human hepatoma cell line R-HepG2. Our study showed that Pa could significantly inhibit the growth of R-HepG2 cells with an IC50 value at 25.0 microM after 48 hours treatment. When compared with the parental HepG2 cells, Pa showed weak resistance to R-HepG2. Efflux of Pa out of R-HepG2 cells was not observed as its cellular uptake level showed no significant difference comparing with HepG2 cells. Interestingly, significant reduction of P-glycoprotein expression on Pa-treated R-HepG2 cells was found at both transcriptional and translational levels, leading to reduction of P-glycoprotein activity. In addition, mechanistic study elucidated that Pa induced cell cycle arrest at G2/M phase and inhibited the expressions of G2/M phase cell cycle regulatory proteins, cyclin-A1 and cdc2 in a dose-dependent manner.

摘要

半枝莲是一种原产于中国南方的传统中药,已被广泛用于治疗肝脏疾病。在本研究中,对半枝莲活性成分脱镁叶绿酸a(Pa)对多药耐药(MDR)人肝癌细胞系R-HepG2的抗增殖作用进行了研究。我们的研究表明,处理48小时后,Pa能够显著抑制R-HepG2细胞的生长,IC50值为25.0微摩尔。与亲代HepG2细胞相比,Pa对R-HepG2显示出较弱的耐药性。未观察到Pa从R-HepG2细胞中流出,因为其细胞摄取水平与HepG2细胞相比无显著差异。有趣的是,在转录和翻译水平上均发现,经Pa处理的R-HepG2细胞上P-糖蛋白表达显著降低,导致P-糖蛋白活性降低。此外,机制研究表明,Pa诱导细胞周期阻滞于G2/M期,并以剂量依赖性方式抑制G2/M期细胞周期调节蛋白细胞周期蛋白A1和细胞周期蛋白依赖性激酶2的表达。

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