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Scutellaria barbata D. Don inhibits growth and induces apoptosis by suppressing IL-6-inducible STAT3 pathway activation in human colorectal cancer cells

机译:半枝莲D. Don通过抑制人结直肠癌细胞中IL-6诱导的STAT3途径的激活来抑制生长并诱导凋亡

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摘要

One of the most critical cellular signal transduction pathways known to malfunction in colorectal cancer is the interleukin-6/signal transducer and activator of transcription 3 (IL-6/STAT3) pathway. Scutellaria barbata D. Don (SB) is well-known traditional medicine in China that targets STAT3 signaling, and it has long been used to treat various types of cancer; however, the precise mechanism of its antitumor activity remains largely unclear. In order to further elucidate this underlying mechanism, an ethanol extract of SB (EESB) in cancer treatment. The aim of the present study was to evaluate the effects of EESB on the IL-6-inducible STAT3 pathway. We tested the dose-response association between EESB, IL-6-induced proliferaion and apoptosis using an MTT assay, colony formation and flow cytometry analysis in vitro. In addition, caspase-9 and caspase-3 activation was determined using a colorimetric assay, the activity of IL-6-induced STAT3 pathway was evaluated using western blot analysis, and the expression levels of cyclin D1, cyclin-dependent kinase 4, Bcl2 and Bcl2-associated X were determined using reverse transcription-polymerase chain reaction and western blot analysis. In the present study it was found that EESB could significantly inhibit the IL-6-mediated increase in STAT3 phosphorylation levels and transcriptional activity in HT-29 human colon carcinoma cells, resulting in the suppression of cell proliferation and the induction of apoptosis. In addition, treatment with EESB markedly inhibited the IL-6-induced upregulation of cyclin D1 and B-cell lymphoma-2, two key target genes of the STAT3 pathway. These results suggest that treatment with EESB could effectively inhibit the proliferation and promote the apoptosis of human colon carcinoma cells via modulation of the IL-6/STAT3 signaling pathway and its target genes.
机译:已知在大肠癌中发生故障的最关键的细胞信号转导途径之一是白介素6 /信号转导子和转录激活因子3(IL-6 / STAT3)通路。半枝莲(Scutellaria barbata D. Don,SB)是中国著名的针对STAT3信号转导的传统药物,长期以来一直用于治疗各种癌症。然而,其抗肿瘤活性的确切机制在很大程度上尚不清楚。为了进一步阐明这种潜在机制,在癌症治疗中使用了SB的乙醇提取物(EESB)。本研究的目的是评估EESB对IL-6诱导的STAT3途径的影响。我们使用MTT分析,集落形成和体外流式细胞术分析测试了EESB,IL-6诱导的增殖和凋亡之间的剂量反应关系。此外,使用比色法确定caspase-9和caspase-3的激活,使用Western blot分析评估IL-6诱导的STAT3途径的活性,以及​​细胞周期蛋白D1,细胞周期蛋白依赖性激酶4,Bcl2的表达水平。使用逆转录-聚合酶链反应和蛋白质印迹分析确定与Bcl2-相关的X和Bcl2-相关的X。在本研究中,发现EESB可以显着抑制HT-29人结肠癌细胞中IL-6介导的STAT3磷酸化水平和转录活性的增加,从而抑制细胞增殖和诱导细胞凋亡。此外,用EESB处理可显着抑制IL-6诱导的细胞周期蛋白D1和B细胞淋巴瘤2的上调,这是STAT3途径的两个关键靶基因。这些结果表明用EESB处理可以通过调节IL-6 / STAT3信号通路及其靶基因来有效抑制人结肠癌细胞的增殖并促进其凋亡。

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