Fukamachi Hiroshi, Ito Kosei, Ito Yoshiaki
Department of Biological Sciences, Graduate School of Science, University of Tokyo, Tokyo 113-0033, Japan.
Biochem Biophys Res Commun. 2004 Aug 13;321(1):58-64. doi: 10.1016/j.bbrc.2004.06.099.
We have previously reported that Runx3, a runt domain transcription factor, is a major growth regulator of gastric epithelial cells, that a lack of RUNX3 function is causally related to the genesis and progression of human gastric cancer, and that expression of RUNX3 is greatly reduced in intestinal metaplasias in human stomachs. Here we examined the differentiation of Runx3-/- mouse gastric epithelial cells and found that some cells differentiated into intestinal type cells, which expressed Cdx2, a transcription factor that has been shown to induce intestinal metaplasia in transgenic mice. Differentiation of intestinal type cells was not found in culture of Runx3+/+ gastric epithelial cells. These results suggest that gastric epithelial cells can differentiate into intestinal type cells, probably due to expression of Cdx2 in them when the function of Runx3 is impaired. The relationship between loss of function of Runx3, formation of intestinal metaplasia, and gastric cancer was discussed.
我们之前曾报道,Runx3(一种 runt 结构域转录因子)是胃上皮细胞的主要生长调节因子,RUNX3 功能的缺失与人类胃癌的发生和发展存在因果关系,并且 Runx3 在人类胃的肠化生中表达大幅降低。在此,我们检测了 Runx3 - / - 小鼠胃上皮细胞的分化情况,发现一些细胞分化为肠型细胞,这些细胞表达 Cdx2(一种已证实在转基因小鼠中可诱导肠化生的转录因子)。在 Runx3 + / + 胃上皮细胞培养物中未发现肠型细胞的分化。这些结果表明,当 Runx3 的功能受损时,胃上皮细胞可能由于其中 Cdx2 的表达而分化为肠型细胞。文中还讨论了 Runx3 功能丧失、肠化生形成与胃癌之间的关系。