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作 者:杨光[1] 李雪飞[1] 崔刚[1] 裘正军[2] 黄陈[2]
机构地区:[1]泰安市中心医院普外科,271000 [2]上海交通大学附属第一人民医院普外科
出 处:《中华肝胆外科杂志》2013年第7期539-543,共5页Chinese Journal of Hepatobiliary Surgery
基 金:国家自然科学基金项目(81101844,81210108027);上海市人才发展资金项目(2012040)
摘 要:目的应用白细胞介素6(IL-6)作用于人胰腺癌细胞株SW1990、Capan-2和沉默STAT3基因的SW1990细胞,观察细胞上皮间质转换相关基因的变化并探讨其机制。方法使用IL-6作用人胰腺癌细胞株SW1990、Capan-2和沉默STAT3基因的SW1990细胞。MTT法检测细胞增殖。荧光定量PCR、RealtimePCR、Westernblot检测STAT3、PSTAT3、Snail、Twist和E—cadher—in基因mRNA和蛋白表达。体外侵袭实验检测细胞的侵袭能力。结果100μg/LIL-6作用人胰腺癌细胞株后,细胞增殖能力增强(P〈0.05)。Westernblot显示P—STAT3的表达增加;荧光定量PCR、Real—timePCR、Westernblot显示SnailmRNA和蛋白表达明显升高(P〈0.05);E—cadherinmRNA和蛋白表达明显降低(P〈0.05);细胞侵袭能力增强。而IL-6作用沉默sTAT3基因的SW1990细胞,Snail和EcadherinmRNA和蛋白表达均无明显改变。结论IL-6可能通过激活STAT3信号转导通路,上调Snail和下调E—eadherin基因表达,促进胰腺癌细胞上皮间质转换,进而增强侵袭能力。Objective To investigate the effects and mechanism of IL 6 on the epithelial to mes- enchymal transition of human pancreatic cancer cells. Methods IL-6 was added into the culture media of human pancreatic cancer cells Capan-2, SW1990, and STAT3-siRNA-SW1990. Cell growth was measured by MTT assays. STAT3, p STAT3, Snail, Twist, and E-cadherin mRNA and protein ex- pression were examined using real-time fluorescence quantitative polymerase chain reaction (RT-PCR) and Western blot, respectively. The invasion abilities of SW1990 and Capan-2 cells were determined by a cell invasion assay in vitro. Results Our results showed that 100 μg/L of IL-6 significantly pro- moted the growth and invasion abilities of Capan-2 and SW1990 cells (P〈0.05). The use of IL 6 not only markedly increased the protein expression of P-STAT3 and Snail, but also greatly decreased the mRNA and protein expression of E cadherin. The use of IL 6 can not change the mRNA and protein expression of Snail and E cadherin. Conclusion Activation of the STAT3 signal transducer pathway with IL-6 can promote the epithelial to mesenchymal transition of pancreatic cancer cells in vitro through up regulation of Snail and down-regulation of E-cadherin expression. Therefore the STAT3 signal transducer may provide a novel therapeutic target for the treatment of pancreatic cancer.
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