Silberg Debra G, Sullivan Jessica, Kang Eugene, Swain Gary P, Moffett Jennifer, Sund Newman J, Sackett Sara D, Kaestner Klaus H
Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
Gastroenterology. 2002 Mar;122(3):689-96. doi: 10.1053/gast.2002.31902.
BACKGROUND & AIMS: Intestinal-type gastric cancer is often preceded by intestinal metaplasia in humans. The genetic events responsible for the transdifferentiation that occurs in intestinal metaplasia are not well understood. Cdx2, a transcription factor whose expression is normally limited to the intestine, has been detected in gastric intestinal metaplasia. Cdx2 induces differentiation of intestinal epithelial cells in vitro; therefore, we sought to establish whether a causal relationship exists between Cdx2 activation and intestinal metaplasia.
Cdx2 expression was directed to the gastric mucosa in transgenic mice using cis-regulatory elements of Foxa3 (Hnf3gamma). Transgenic mice were analyzed for histologic and gene expression changes.
Histologic examination of the gastric mucosa of the Foxa3/Cdx2 mice revealed the presence of alcian blue-positive intestinal-type goblet cells, a hallmark of intestinal metaplasia. In addition, Cdx2 induced the expression of intestine-specific genes.
Gastric expression of Cdx2 alone was sufficient to induce intestinal metaplasia in mice. These mice represent a powerful tool to investigate the molecular mechanisms that promote intestinal metaplasia. Moreover, as gastric cancer in humans is often preceded by intestinal metaplasia, the phenotype described here strongly suggests involvement of Cdx2 in the initiation of the process leading to intestinal neoplasia of the gastric mucosa.
在人类中,肠型胃癌常由肠化生发展而来。导致肠化生过程中发生转分化的基因事件尚不清楚。Cdx2是一种转录因子,其表达通常局限于肠道,但在胃肠化生中也有发现。Cdx2在体外可诱导肠上皮细胞分化;因此,我们试图确定Cdx2激活与肠化生之间是否存在因果关系。
利用Foxa3(Hnf3γ)的顺式调控元件,将Cdx2的表达定向到转基因小鼠的胃黏膜中。对转基因小鼠进行组织学和基因表达变化分析。
对Foxa3/Cdx2小鼠胃黏膜的组织学检查发现,存在阿利新蓝阳性的肠型杯状细胞,这是肠化生的一个标志。此外,Cdx2诱导了肠道特异性基因的表达。
单独在胃中表达Cdx2足以在小鼠中诱导肠化生。这些小鼠是研究促进肠化生分子机制的有力工具。此外,由于人类胃癌常由肠化生发展而来,此处描述的表型强烈提示Cdx2参与了导致胃黏膜肠肿瘤形成过程的起始阶段。