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首页> 外文期刊>Hormone and Metabolic Research >Formononetin-induced apoptosis by activation of Ras/p38 mitogen-activated protein kinase in estrogen receptor-positive human breast cancer cells
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Formononetin-induced apoptosis by activation of Ras/p38 mitogen-activated protein kinase in estrogen receptor-positive human breast cancer cells

机译:Formononetin通过激活Ras / p38丝裂原激活的蛋白激酶在雌激素受体阳性的人乳腺癌细胞中诱导的凋亡

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Formononetin is one of the main active components of red clover plants, and considered as a phytoestrogen. Its pharmacological effects in vivo may be either estrogenic or anti-estrogenic, mainly depending upon the estrogen levels. Our recent studies suggested that formononetin inactivated IGF1/IGF1R-PI3K/Akt pathways and decreased cyclin D1 mRNA and protein expression in human breast cancer cells in vitro and in vivo. In the present study, we further investigated the molecular mechanisms involved in the induced apoptosis effect of formononetin on breast cancer cells. Our results suggested that formononetin inhibited the proliferation of ER-positive MCF-7 cells and T47D cells. In contrast, formononetin could not inhibit the cell of growth of ER-negative breast cancer cells such as MDA-MB-435 S cells. We further found that formononetin activated MAPK signaling pathway in a dose-dependent manner, which resulted in the increased ratio of Bax/Bcl-2, and induced apoptosis on MCF-7 cells. However, when MCF-7 cells were pretreated with p38MAPK inhibitor SB203580 before formononetin, apoptosis induced by formononetin was significantly attenuated. Thus, we conclude that the induced apoptosis effect of formononetin on human breast cancer cells were related to Ras-p38MAPK pathway. Considering that red clover plants are widely used clinically, our results provide the foundation for future development of formononetin for treatment of ER-positive breast cancer.
机译:福莫尼汀是红三叶草植物的主要活性成分之一,被认为是植物雌激素。其在体内的药理作用可能是雌激素的或抗雌激素的,主要取决于雌激素水平。我们最近的研究表明,formononetin可以在体外和体内使人乳腺癌细胞中的IGF1 / IGF1R-PI3K / Akt通路失活,并降低cyclin D1 mRNA和蛋白质的表达。在本研究中,我们进一步研究了Formononetin诱导乳腺癌细胞凋亡的分子机制。我们的结果表明formononetin抑制ER阳性MCF-7细胞和T47D细胞的增殖。相比之下,formononetin不能抑制ER阴性乳腺癌细胞(如MDA-MB-435 S细胞)的生长。我们进一步发现formononetin以剂量依赖的方式激活MAPK信号通路,从而导致Bax / Bcl-2的比率增加,并诱导MCF-7细胞凋亡。然而,当在formononetin之前用p38MAPK抑制剂SB203580预处理MCF-7细胞时,formononetin诱导的细胞凋亡被显着减弱。因此,我们得出结论,Formononetin对人乳腺癌细胞的诱导凋亡作用与Ras-p38MAPK通路有关。考虑到红三叶草在临床上得到了广泛应用,我们的结果为将来开发的formononetin用于治疗ER阳性乳腺癌提供了基础。

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