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首页> 外文期刊>Journal of experimental & clinical cancer research : >Effects of IL-6 and AG490 on regulation of Stat3 signaling pathway and invasion of human pancreatic cancer cells in vitro
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Effects of IL-6 and AG490 on regulation of Stat3 signaling pathway and invasion of human pancreatic cancer cells in vitro

机译:IL-6和AG490对Stat3信号通路的调控及对人胰腺癌细胞侵袭的影响。

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Background Signal transducer and activator of transcription 3 (Stat3) is a member of the Janus-activated kinase(Jak)/Stat signaling pathway. Abnormal activation of Stat3 plays a critical role in metastasis and invasion in varieties of human tumors including pancreatic cancer. This study aimed to investigate the mechanisms of activation and blocking of the Stat3 signaling pathway and its effects on invasion and metastasis of human pancreatic cancer cells. Methods The Jak inhibitor AG490 and interleukin-6 (IL-6) were added to the culture media of human pancreatic cancer cells SW1990 and Capan-2, respectively. Cell growth was measured by MTT assays. Western blotting and immunocytochemistry were performed to detect phosphorylated Stat3 (p-Stat3) protein, while VEGF and MMP-2 mRNA and protein expression were examined with fluorescence quantitative polymerase chain reaction and Western blotting, respectively. The invasion ability of SW1990 and Capan-2 cells was determined by cell invasion assay. Results Stat3 was activated by IL-6 in Capan-2 cells; protein expression of p-Stat3 was increased significantly in Capan-2 cells. IL-6 remarkably promoted the growth of Capan-2 cells (P P Conclusions Abnormal activation of Stat3 plays an important role in the invasion and metastasis of pancreatic cancer. Activation and blocking of the Stat3 signaling pathway can affect invasion ability and expression of the VEGF and MMP-2 genes in pancreatic cancer cells. The Stat3 signaling pathway may provide a novel therapeutic target for treatment of pancreatic cancer.
机译:背景信号转导子和转录激活子3(Stat3)是Janus激活的激酶(Jak)/ Stat信号通路的成员。 Stat3的异常激活在包括胰腺癌在内的多种人类肿瘤的转移和侵袭中起着关键作用。这项研究旨在调查Stat3信号通路的激活和阻断机制及其对人胰腺癌细胞侵袭和转移的影响。方法将Jak抑制剂AG490和白细胞介素6(IL-6)分别加入人胰腺癌细胞SW1990和Capan-2的培养基中。细胞生长通过MTT测定法测量。进行蛋白质印迹和免疫细胞化学检测,以检测磷酸化的Stat3(p-Stat3)蛋白,同时分别通过荧光定量聚合酶链反应和蛋白质印迹检测VEGF和MMP-2 mRNA和蛋白表达。通过细胞侵袭测定法确定SW1990和Capan-2细胞的侵袭能力。结果IL-6在Capan-2细胞中激活Stat3。 Capan-2细胞中p-Stat3的蛋白表达显着增加。 IL-6显着促进Capan-2细胞的生长(PP结论)Stat3的异常激活在胰腺癌的侵袭和转移中起着重要的作用。Stat3信号通路的激活和阻断会影响胰腺癌的侵袭能力和表达。胰腺癌细胞中的MMP-2基因Stat3信号通路可能为胰腺癌的治疗提供新的靶点。

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