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黄芩苷是黄芩的一种成分,它通过下调人胰腺癌细胞中的Mcl-1诱导细胞凋亡。

Baicalein, a component of Scutellaria baicalensis, induces apoptosis by Mcl-1 down-regulation in human pancreatic cancer cells.

作者信息

Takahashi Hiroki, Chen Monica C, Pham Hung, Angst Eliane, King Jonathan C, Park Jenny, Brovman Ethan Y, Ishiguro Hideyuki, Harris Diane M, Reber Howard A, Hines Oscar J, Gukovskaya Anna S, Go Vay Liang W, Eibl Guido

机构信息

Department of Surgery, UCLA Center for Excellence in Pancreatic Diseases, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.

出版信息

Biochim Biophys Acta. 2011 Aug;1813(8):1465-74. doi: 10.1016/j.bbamcr.2011.05.003. Epub 2011 May 10.

Abstract

Scutellaria baicalensis (SB) and SB-derived polyphenols possess anti-proliferative activities in several cancers, including pancreatic cancer (PaCa). However, the precise molecular mechanisms have not been fully defined. SB extract and SB-derived polyphenols (wogonin, baicalin, and baicalein) were used to determine their anti-proliferative mechanisms. Baicalein significantly inhibited the proliferation of PaCa cell lines in a dose-dependent manner, whereas wogonin and baicalin exhibited a much less robust effect. Treatment with baicalein induced apoptosis with release of cytochrome c from mitochondria, and activation of caspase-3 and -7 and PARP. The general caspase inhibitor zVAD-fmk reversed baicalein-induced apoptosis, indicating a caspase-dependent mechanism. Baicalein decreased expression of Mcl-1, an anti-apoptotic member of the Bcl-2 protein family, presumably through a transcriptional mechanism. Genetic knockdown of Mcl-1 resulted in marked induction of apoptosis. The effect of baicalein on apoptosis was significantly attenuated by Mcl-1 over-expression, suggesting a critical role of Mcl-1 in this process. Our results provide evidence that baicalein induces apoptosis in pancreatic cancer cells through down-regulation of the anti-apoptotic Mcl-1 protein.

摘要

黄芩(SB)及其衍生的多酚在包括胰腺癌(PaCa)在内的多种癌症中具有抗增殖活性。然而,确切的分子机制尚未完全明确。使用黄芩提取物及其衍生的多酚(汉黄芩素、黄芩苷和黄芩素)来确定它们的抗增殖机制。黄芩素以剂量依赖性方式显著抑制PaCa细胞系的增殖,而汉黄芩素和黄芩苷的作用则弱得多。用黄芩素处理可诱导细胞凋亡,伴有细胞色素c从线粒体释放,以及半胱天冬酶-3、-7和聚(ADP-核糖)聚合酶(PARP)的激活。通用的半胱天冬酶抑制剂zVAD-fmk可逆转黄芩素诱导的细胞凋亡,表明这是一种依赖半胱天冬酶的机制。黄芩素可能通过转录机制降低Bcl-2蛋白家族的抗凋亡成员Mcl-1的表达。Mcl-1的基因敲低导致明显的细胞凋亡诱导。Mcl-1的过表达显著减弱了黄芩素对细胞凋亡的作用,表明Mcl-1在此过程中起关键作用。我们的结果提供了证据,证明黄芩素通过下调抗凋亡的Mcl-1蛋白诱导胰腺癌细胞凋亡。

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