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机构地区:[1]徐州医学院研究生学院2011级,江苏徐州221004 [2]徐州医学院病理学教研室
出 处:《徐州医学院学报》2014年第4期258-261,共4页Acta Academiae Medicinae Xuzhou
基 金:江苏省高校自然科学基金(12KJD320006,07KJD310217);徐州市科技局项目(XF11C1002011)
摘 要:目的探究三氧化二砷(As2O3)对侵袭相关因子β—catenin表达的影响是否与FOXO3a有关。方法采用脂质体转染siRNA以及LY294002药物改变大肠癌SW620细胞中FOXO3a的表达,Western blot检测FOXO3a、β—catenin蛋白表达水平,RT—PCR检测FOXO3a、β—catenin mRNA表达水平。结果As2O3增加SW620细胞中FOXO3a蛋白及mRNA的表达,同时降低β—catenin蛋白及mRNA表达(P〈0.05)。FOXO3a基因干扰后,β—catenin蛋白及mRNA的表达上调(P〈0.05)。LY294002药物处理后,β—catenin表达下调(P〈0.05)。结论As2O3对人大肠癌SW620细胞中β—catenin表达的抑制作用可能与其增强FOXO3a的活性有关。Objective To investigate whether FOXO3a is involved in the changed expression of β - catenin in colorectal cancer SW620 ceils after exposure to arsenic trioxide ( As2O3 ). Methods The expression of FOXO3a was changed by FOXO3a specific siRNA and LY294002. Then, the protein and mRNA expressions of FOXO3a and β- catenin in eoloreetal cancer SW620 cells were detected by western blot and RT -PCR, respectively. Results As2O3 can stimulate the protein and mRNA expressions of FOXO3a in SW620 cells, while reducing the expression of β - catenin at protein and mRNA levels (P 〈 0.05 ). After FOXO3a gene silencing, the protein and mRNA expressions of β -catenin were obviously enhanced ( P 〈 0.05 ). But LY294002 treatment could remarkably inhibit the expression of β - catenin at protein and mRNA levels. Conclusion The inhibitory effects of As2O3 on β - eatenin in eolorectal cancer SW620 cells may be associate with its ability to enhance the activity of FOXO3a.
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