...
首页> 外文期刊>Journal of biomedical science. >Resistin-induced stromal cell-derived factor-1 expression through Toll-like receptor 4 and activation of p38 MAPK/ NFκB signaling pathway in gastric cancer cells
【24h】

Resistin-induced stromal cell-derived factor-1 expression through Toll-like receptor 4 and activation of p38 MAPK/ NFκB signaling pathway in gastric cancer cells

机译:抵抗素通过Toll样受体4诱导基质细胞衍生因子-1的表达和p38 MAPK /NFκB信号通路在胃癌细胞中的激活

获取原文
           

摘要

BackgroundStromal cell-derived factor-1 (SDF-1) (CXC chemokine ligand-12)/CXC chemokine receptor 4 (CXCR4) is involved in the carcinogenesis of human gastric cancer, where it stimulates angiogenesis and favors metastasis of tumor cells to distant organs. In addition, resistin is suggested to be an important link between obesity and the development of gastric cancer. Resistin has identified as an important player in inflammatory responses, and emerged as a mediator in inflammation-associated cancer. A limited number of studies have investigated the association of resistin and SDF-1 with gastric cancer. Herein, we investigated the molecular mechanisms by which resistin influences the expression of SDF-1 in gastric carcinoma cells.ResultsHuman gastric cancer cell lines were exposed to doses of resistin; SDF-1 expression and secretion levels were then determined. Real-time polymerase chain reaction and western blotting analyses were performed to clarify molecular changes. Inhibition of Toll-like receptor 4 (TLR4) by a competitive antagonist inhibited resistin-induced SDF-1 expression. Pharmacological inhibitors and small interfering RNA (siRNA) demonstrated that activation of the p38 mitogen-activated protein kinase (MAPK) pathway is critical for resistin-induced SDF-1 expression mediated by TLR4. The promoter activity and transcription factor enzyme-linked immunosorbent assay revealed that resistin induced expression of SDF-1 mediated by NF-κB in gastric cancer cells. Inhibition of p38 MARK activation blocked the SDF-1-induced expression and the SDF-1 promoter activity in the cancer gastric cells. Chromatin immunoprecipitation assay revealed that inhibition of p38 MARK activation also blocked the resistin-increased NF-κB-DNA-binding activity.ConclusionsResistin-induced SDF-1 upregulation by activation of TLR4, p38 MARK and NF-κB may explain a new role of resistin in the link of obesity and gastric cancer.
机译:背景星形细胞衍生因子1(SDF-1)(CXC趋化因子配体12)/ CXC趋化因子受体4(CXCR4)参与人类胃癌的癌变过程,它刺激血管生成并促进肿瘤细胞向远处器官的转移。 。另外,抵抗素被认为是肥胖与胃癌发展之间的重要联系。抵抗素已被确定为炎症反应的重要参与者,并已成为炎症相关癌症的介体。有限的研究已经调查了抵抗素和SDF-1与胃癌的关系。本文探讨了抵抗素影响胃癌细胞中SDF-1表达的分子机制。然后确定SDF-1的表达和分泌水平。进行实时聚合酶链反应和蛋白质印迹分析以阐明分子变化。竞争性拮抗剂对Toll样受体4(TLR4)的抑制作用抑制了抵抗素诱导的SDF-1表达。药理抑制剂和小干扰RNA(siRNA)证明,p38丝裂原活化蛋白激酶(MAPK)途径的激活对于由TLR4介导的抵抗素诱导的SDF-1表达至关重要。启动子活性和转录因子酶联免疫吸附试验表明,抵抗素诱导了NF-κB介导的胃癌细胞中SDF-1的表达。 p38 MARK激活的抑制作用阻止了癌细胞胃癌细胞中SDF-1诱导的表达和SDF-1启动子活性。染色质免疫沉淀实验表明,抑制p38 MARK的活化也阻断了抵抗素增加的NF-κB-DNA结合活性。在肥胖和胃癌的联系。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号