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Casticin induces breast cancer cell apoptosis by inhibiting the expression of forkhead box protein M1

机译:Casticin通过抑制叉头盒蛋白M1的表达诱导乳腺癌细胞凋亡

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摘要

Casticin is an active ingredient derived from Fructus Viticis, a traditional Chinese medicine. This study aimed to investigate the role of forkhead box O3 (FOXO3a) in breast cancer cells and examine the regulatory mechanisms of FOXO3a in response to casticin treatment of the cells by ELISA, flow cytometry, small interfering RNA (siRNA) transfection and western blot analysis. Casticin treatment induced apoptosis and reduced the expression of the transcription factor forkhead box protein M1 (FOXM1). In addition, FOXM1 repression induced by casticin treatment was associated with the activation of FOXO3a via increased dephosphorylation. Notably, silencing FOXO3a expression by siRNA-mediated gene knockdown attenuated casticin-mediated apoptosis. Collectively, these findings suggest that FOXO3a is a critical mediator of the inhibitory effects of casticin on apoptosis in breast cancer cells.
机译:卡斯汀是从中药苦果中提取的有效成分。这项研究旨在调查叉头盒O3(FOXO3a)在乳腺癌细胞中的作用,并通过ELISA,流式细胞术,小干扰RNA(siRNA)转染和Western blot分析法检查FOXO3a响应卡西汀处理细胞的作用。 Casticin处理诱导凋亡,并降低转录因子叉头盒蛋白M1(FOXM1)的表达。此外,由卡斯汀处理诱导的FOXM1抑制与FOXO3a的活化通过增加的去磷酸化有关。值得注意的是,通过siRNA介导的基因敲低使FOXO3a表达沉默,从而减弱了Casticin介导的细胞凋亡。总的来说,这些发现表明FOXO3a是casticin抑制乳腺癌细胞凋亡的关键介质。

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