Fukamachi Hiroshi, Ito Kosei
Department of Biological Sciences, Graduate School of Science, University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Oncogene. 2004 May 24;23(24):4330-5. doi: 10.1038/sj.onc.1207121.
RUNX3: is expressed by gastric epithelial cells throughout development. Mice whose Runx3 gene has been knocked out died soon after birth. In the knockout mouse, gastric epithelia exhibited hyperplasia and epithelial apoptosis was suppressed. Analysis using a primary culture system for the epithelial cells suggested that this is caused by the reduced sensitivity of Runx3-/- gastric epithelial cells to the growth-inhibiting and apoptosis-inducing activities of TGF-beta. In human and mouse gastric cancer cell lines, RUNX3/Runx3 was silenced due to hypermethylation of CpG islands in the promoter region. Exogenous expression of RUNX3 in the cells that do not express the endogenous gene caused an inhibition of growth both in vivo and in vitro. These observations indicate that Runx3 is a major growth regulator of gastric epithelial cells, and that it is deeply involved in gastric tumorigenesis in both humans and mice.
RUNX3:在整个发育过程中由胃上皮细胞表达。Runx3基因被敲除的小鼠在出生后不久死亡。在基因敲除小鼠中,胃上皮出现增生,上皮细胞凋亡受到抑制。使用上皮细胞原代培养系统进行的分析表明,这是由于Runx3基因敲除的胃上皮细胞对转化生长因子-β(TGF-β)的生长抑制和凋亡诱导活性的敏感性降低所致。在人和小鼠胃癌细胞系中,由于启动子区域CpG岛的高甲基化,RUNX3/Runx3被沉默。在不表达内源性基因的细胞中外源表达RUNX3导致体内和体外生长均受到抑制。这些观察结果表明,Runx3是胃上皮细胞的主要生长调节因子,并且它在人类和小鼠的胃癌发生中都有深入参与。