首页> 外文期刊>Oncology Research >Tea polyphenols induce apoptosis through mitochondrial pathway and by inhibiting nuclear factor-kappaB and Akt activation in human cervical cancer cells.
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Tea polyphenols induce apoptosis through mitochondrial pathway and by inhibiting nuclear factor-kappaB and Akt activation in human cervical cancer cells.

机译:茶多酚通过线粒体途径以及抑制人宫颈癌细胞中的核因子-κB和Akt活化来诱导细胞凋亡。

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Phytochemicals present in tea, particularly polyphenols, have anticancer properties against several cancer types. However, studies elucidating the role and the mechanism(s) of action of tea polyphenols in cervical cancer are sparse. In this study, we investigated the mechanism of antiproliferative and apoptotic actions exerted by tea polyphenols on human papilloma virus-18-positive HeLa cervical cancer cells. Treatment of green tea polyphenol (-)-epigallocatechin gallate (EGCG) and black tea polyphenol theaflavins (TF) in HeLa cells showed a marked concentration- and time-dependent inhibition of proliferation and induced sub-G1 phase in a dose-dependent manner after 24 h. There was an attenuation of mitochondrial membrane potential with the increase of reactive oxygen species generation, p53 expression, Bax/Bcl-2 ratio, cytochrome-c release, and cleavage of procaspase-3 and -9 and poly(ADP-ribose)-polymerase, indicating the participation of a mitochondria related mechanism. In addition, EGCG as well as TF inhibited activation of Akt and nuclear factor-kappaB (NF-kappaB) via blocking phosphorylation and subsequent degradation of inhibitor of kappaBalpha and kappaBbeta subunits, thereby downregulating cyclooxygenase-2. Additionally, the protein level of cyclin D1, a transcriptional target of NF-kappaB, was also reduced significantly. Thus, we can conclude that tea polyphenols inhibit the growth of cervical cancer cells by inducing apoptosis and regulating NF-kappaB and Akt.
机译:茶中存在的植物化学物质,特别是多酚,具有抗多种癌症的抗癌特性。然而,阐明茶多酚在宫颈癌中的作用和作用机理的研究很少。在这项研究中,我们研究了茶多酚对人乳头瘤病毒18阳性HeLa宫颈癌细胞的抗增殖和凋亡作用的机制。在HeLa细胞中对绿茶多酚(-)-表没食子儿茶素没食子酸酯(EGCG)和红茶多酚茶黄素(TF)的处理显示出浓度和时间依赖性的增殖抑制和诱导的Sub-G1期以剂量依赖性方式明显抑制24小时随着活性氧的产生,p53表达,Bax / Bcl-2比,细胞色素c释放,procaspase-3和-9以及聚(ADP-核糖)聚合酶的裂解增加,线粒体膜电位降低。 ,表明线粒体相关机制的参与。此外,EGCG和TF通过阻止磷酸化和随后的kappaBalpha和kappaBbeta亚基抑制剂的降解来抑制Akt和核因子kappaB(NF-kappaB)的激活,从而下调环氧合酶2。此外,细胞周期蛋白D1(NF-κB的转录靶标)的蛋白水平也显着降低。因此,我们可以得出结论,茶多酚通过诱导凋亡和调节NF-κB和Akt抑制宫颈癌细胞的生长。

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