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Oncogenic ras induces gastrin/CCKB receptor gene expression in human colon cancer cell lines LoVo and Colo320HSR

机译:肿瘤内ras诱导人结肠癌细胞系Lovo和colo320hsr中的胃泌素/ cckb受体基因表达

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摘要

Gastrin has the ability to stimulate cell growth in some colorectal cancer cells and some of these cells also express gastrin/CCKB receptors, suggesting that gastrin and its autocrine loop are involved in their proliferation. We previously reported that oncogenic ras induced gastrin gene expression in colon cancer cells. The aim of this study was to investigate whether oncogenic ras also induces gastrin/CCKB receptor gene expression. A transiently transfected activated ras vector stimulated gastrin/CCKB receptor transcriptional activities in both Colo320HSR and LoVo cells, but these ras-increased activities were inhibited by a specific MEK inhibitor, PD98059. An RPA demonstrated that activated ras increased endogenous gastrin/CCKB receptor mRNA levels and PD98059 decreased them in LoVo cells. These findings suggest that oncogenic ras induces gastrin/CCKB receptor gene expression through some intracellular signaling pathways, including MEK, in colon cancer cell lines.
机译:胃泌素具有刺激某些结肠直肠癌细胞生长的能力,其中一些细胞还表达胃泌素/ CCKB受体,表明胃泌素及其自分泌环参与其增殖。我们先前曾报道致癌性ras诱导结肠癌细胞中胃泌素基因表达。这项研究的目的是调查致癌性ras是否还诱导胃泌素/ CCKB受体基因表达。瞬时转染的活化ras载体在Colo320HSR和LoVo细胞中均刺激了胃泌素/ CCKB受体的转录活性,但是这些ras增强的活性被特定的MEK抑制剂PD98059抑制。 RPA表明,活化的ras增加了LoVo细胞的内源性胃泌素/ CCKB受体mRNA水平,而PD98059降低了它们。这些发现表明,致癌性ras通过结肠癌细胞系中的一些细胞内信号传导途径,包括MEK,诱导胃泌素/ CCKB受体基因表达。

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