Suppr超能文献

胃泌素通过 CCK2 受体增加胃肠道癌细胞自身的合成。

Gastrin increases its own synthesis in gastrointestinal cancer cells via the CCK2 receptor.

机构信息

The University of Melbourne, Department of Surgery, Austin Health, Heidelberg, Victoria, Australia.

出版信息

FEBS Lett. 2010 Nov 5;584(21):4413-8. doi: 10.1016/j.febslet.2010.09.046. Epub 2010 Oct 8.

Abstract

The involvement of the gastrointestinal hormone gastrin in the development of gastrointestinal cancer is highly controversial. Here we demonstrate a positive-feedback loop whereby gastrin, acting via the CCK2 receptor, increases its own expression. Such an autocrine loop has not previously been reported for any other gastrointestinal hormone. Gastrin promoter activation was dependent on the MAP kinase pathway and did not involve Sp1 binding sites or epidermal growth factor receptor transactivation. As the treatment of gastrointestinal cancer cells with amidated gastrin led to increased expression of non-amidated gastrins, the positive-feedback loop may contribute to the sustained increase in circulating gastrins observed in colorectal cancer patients.

摘要

胃肠道激素胃泌素在胃肠道癌症发展中的作用存在很大争议。在这里,我们证明了一个正反馈回路,即胃泌素通过 CCK2 受体作用,增加自身的表达。这种自分泌回路以前尚未在任何其他胃肠道激素中报道过。胃泌素启动子的激活依赖于 MAP 激酶途径,不涉及 Sp1 结合位点或表皮生长因子受体的反式激活。由于用酰胺化胃泌素处理胃肠道癌细胞会导致非酰胺化胃泌素的表达增加,因此正反馈回路可能有助于解释在结直肠癌患者中观察到的循环胃泌素的持续增加。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验