Hsieh Yung-Yu, Shen Chien-Heng, Huang Wen-Shih, Chin Chih-Chien, Kuo Yi-Hung, Hsieh Meng Chiao, Yu Hong-Ren, Chang Te-Sheng, Lin Tseng-Hsi, Chiu Yung-Wei, Chen Cheng-Nan, Kuo Hsing-Chun, Tung Shui-Yi
Department of Hepato-Gastroenterology, Chang Gung Memorial Hospital, Chiayi, Taiwan.
J Biomed Sci. 2014 Jun 14;21(1):59. doi: 10.1186/1423-0127-21-59.
Stromal 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.
Human 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.
Resistin-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.
基质细胞衍生因子-1(SDF-1)(CXC趋化因子配体-12)/CXC趋化因子受体4(CXCR4)参与人类胃癌的致癌过程,它可刺激血管生成并促进肿瘤细胞向远处器官转移。此外,抵抗素被认为是肥胖与胃癌发生之间的重要联系。抵抗素已被确定为炎症反应中的重要参与者,并成为炎症相关癌症的介质。少数研究调查了抵抗素和SDF-1与胃癌的关联。在此,我们研究了抵抗素影响胃癌细胞中SDF-1表达的分子机制。
将人胃癌细胞系暴露于不同剂量的抵抗素;然后测定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。用竞争性拮抗剂抑制Toll样受体4(TLR4)可抑制抵抗素诱导的SDF-1表达。药理学抑制剂和小干扰RNA(siRNA)表明,p38丝裂原活化蛋白激酶(MAPK)途径的激活对于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测定显示,抵抗素诱导胃癌细胞中由核因子κB(NF-κB)介导的SDF-1表达。抑制p38 MAPK激活可阻断胃癌细胞中SDF-1诱导的表达和SDF-1启动子活性。染色质免疫沉淀测定显示,抑制p38 MAPK激活也可阻断抵抗素增加的NF-κB-DNA结合活性。
抵抗素通过激活TLR4、p38 MAPK和NF-κB诱导SDF-1上调,这可能解释了抵抗素在肥胖与胃癌联系中的新作用。