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首页> 外文期刊>World Journal of Gastroenterology >Lysophosphatidic acid transactivates both c-Met and epidermal growth factor receptor, and induces cyclooxygenase-2 expression in human colon cancer LoVo cells.
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Lysophosphatidic acid transactivates both c-Met and epidermal growth factor receptor, and induces cyclooxygenase-2 expression in human colon cancer LoVo cells.

机译:溶血磷脂酸可同时激活c-Met和表皮生长因子受体,并诱导人结肠癌LoVo细胞中环氧合酶2的表达。

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摘要

AIM: To examine whether lysophosphatidic acid (LPA) induces phosphorylation of c-Met and epidermal growth factor receptor (EGFR), both of which have been proposed as prognostic markers of colorectal cancer, and whether LPA induces cyclooxygenase-2 (COX-2) expression in human colon cancer cells. METHODS: Using a human colon cancer cell line, LoVo cells, we performed immunoprecipitation analysis, followed by Western blot analysis. We also examined whether LPA induced COX-2 expression, by Western blot analysis. RESULTS: Immunoprecipitation analysis revealed that 10 mumol/L LPA induced tyrosine phosphorylation of c-Met and EGFR in LoVo cells within a few minutes. We found that c-Met tyrosine phosphorylation induced by LPA was not attenuated by pertussis toxin or a matrix metalloproteinase inhibitor, in marked contrast to the results for EGFR. In addition, 0.2-40 mumol/L LPA induced COX-2 expression in a dose-dependent manner. CONCLUSION: Our results suggest that LPA acts upstream of various receptor tyrosine kinases (RTKs) and COX-2, and thus may act as a potent stimulator of colorectal cancer.
机译:目的:研究溶血磷脂酸(LPA)是否诱导c-Met和表皮生长因子受体(EGFR)的磷酸化,两者均被提议作为大肠癌的预后指标,LPA是否诱导环氧合酶-2(COX-2)在人类结肠癌细胞中的表达。方法:使用人结肠癌细胞系LoVo细胞,我们进行了免疫沉淀分析,然后进行蛋白质印迹分析。我们还通过蛋白质印迹分析检查了LPA是否诱导了COX-2表达。结果:免疫沉淀分析表明,在几分钟内,10μmol/ L LPA诱导LoVo细胞中c-Met和EGFR的酪氨酸磷酸化。我们发现,由LPA诱导的c-Met酪氨酸磷酸化没有被百日咳毒素或基质金属蛋白酶抑制剂减弱,这与EGFR的结果形成鲜明对比。另外,0.2-40μmol/ L LPA以剂量依赖性方式诱导COX-2表达。结论:我们的结果表明,LPA在各种受体酪氨酸激酶(RTK)和COX-2的上游起作用,因此可能是结直肠癌的有效刺激剂。

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