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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Inhibition of STAT3 by RNA interference suppresses angiogenesis in colorectal carcinoma
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Inhibition of STAT3 by RNA interference suppresses angiogenesis in colorectal carcinoma

机译:RNA干扰抑制STAT3抑制大肠癌血管生成

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摘要

In order to investigate signal transduction and activation of transcription 3 (STAT3) signaling on angiogenesis in colorectal carcinoma (CRC) after inhibiting STAT3 expression, we constructed the HT-29-shSTAT3 cell line by lentivirus-mediated RNAi. Cell growth was assessed with MTT and the cell cycle distribution by flow cytometry. CRC nude mouse models were established and tumor growth was monitored periodically. On day 30, all mice were killed and tumor tissues were removed. Microvessel density (MVD) was determined according to CD34-positive staining. The expression of vascular endothelial growth factor A (VEGFA), matrix metalloproteinase-2 (MMP2) and basic fibroblast growth factor (FGF2) was monitored by quantitative real-time PCR and Western blot analysis. Knockdown of STAT3 expression significantly inhibited cell growth in HT-29 cells, with a significantly higher proportion of cells at G0/G1 (P 0.05). Taken together, these results demonstrate that STAT3 signaling is important to the growth of CRC and promotes angiogenesis by regulating VEGFA and MMP2 expression.
机译:为了研究抑制STAT3表达后大肠癌(CRC)中血管生成的信号转导和转录3(STAT3)信号的激活,我们通过慢病毒介导的RNAi构建了HT-29-shSTAT3细胞系。用MTT评估细胞生长,并通过流式细胞术评估细胞周期分布。建立CRC裸鼠模型并定期监测肿瘤生长。在第30天,杀死所有小鼠并去除肿瘤组织。根据CD34阳性染色确定微血管密度(MVD)。通过实时荧光定量PCR和Western印迹分析监测血管内皮生长因子A(VEGFA),基质金属蛋白酶-2(MMP2)和碱性成纤维细胞生长因子(FGF2)的表达。抑制STAT3表达可显着抑制HT-29细胞的细胞生长,在G0 / G1处细胞比例显着更高(P 0.05)。综上所述,这些结果表明STAT3信号传导对CRC的生长很重要,并通过调节VEGFA和MMP2的表达促进血管生成。

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