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熊果酸可诱导MCF-7乳腺癌细胞凋亡并下调Bcl-2蛋白表达。

Ursolic acid triggers apoptosis and Bcl-2 downregulation in MCF-7 breast cancer cells.

作者信息

Kassi E, Sourlingas T G, Spiliotaki M, Papoutsi Z, Pratsinis H, Aligiannis N, Moutsatsou P

机构信息

Laboratory of Biological Chemistry, Medical School, University of Athens, Athens, Greece.

出版信息

Cancer Invest. 2009 Aug;27(7):723-33. doi: 10.1080/07357900802672712.

Abstract

In this report we determine the ability of ursolic acid (UA) to induce apoptosis and to modulate glucocorticoid receptor (GR) and Activator Protein-1 (AP-1) in MCF-7 cells. The UA-induced apoptosis (53 microM), the PARP cleavage, and the decrease in Bcl-2 protein (53 microM) support the notion that UA induces apoptosis through the intrinsic mitochondrial pathway. UA binds GR (relative binding affinity: 2.57) and translocates GR into nucleus, suggesting its potential as a GR modulator. UA had no effect on GRE- or TRE-driven gene expression. In summary, UA is a GR modulator and may be considered as a potential anticancer agent in breast cancer.

摘要

在本报告中,我们测定了熊果酸(UA)诱导MCF-7细胞凋亡以及调节糖皮质激素受体(GR)和活化蛋白-1(AP-1)的能力。UA诱导的凋亡(53微摩尔)、PARP裂解以及Bcl-2蛋白减少(53微摩尔)支持了UA通过内在线粒体途径诱导凋亡的观点。UA与GR结合(相对结合亲和力:2.57)并将GR转运至细胞核,表明其作为GR调节剂的潜力。UA对GRE或TRE驱动的基因表达没有影响。总之,UA是一种GR调节剂,可被视为乳腺癌潜在的抗癌剂。

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