Suppr超能文献

鉴定c-MYC为APC通路的一个靶点。

Identification of c-MYC as a target of the APC pathway.

作者信息

He T C, Sparks A B, Rago C, Hermeking H, Zawel L, da Costa L T, Morin P J, Vogelstein B, Kinzler K W

机构信息

Howard Hughes Medical Institute and Johns Hopkins Oncology Center, 424 North Bond Street, Baltimore, MD 21231, USA.

出版信息

Science. 1998 Sep 4;281(5382):1509-12. doi: 10.1126/science.281.5382.1509.

Abstract

The adenomatous polyposis coli gene (APC) is a tumor suppressor gene that is inactivated in most colorectal cancers. Mutations of APC cause aberrant accumulation of beta-catenin, which then binds T cell factor-4 (Tcf-4), causing increased transcriptional activation of unknown genes. Here, the c-MYC oncogene is identified as a target gene in this signaling pathway. Expression of c-MYC was shown to be repressed by wild-type APC and activated by beta-catenin, and these effects were mediated through Tcf-4 binding sites in the c-MYC promoter. These results provide a molecular framework for understanding the previously enigmatic overexpression of c-MYC in colorectal cancers.

摘要

腺瘤性结肠息肉病基因(APC)是一种肿瘤抑制基因,在大多数结直肠癌中失活。APC突变导致β-连环蛋白异常积累,β-连环蛋白随后与T细胞因子4(Tcf-4)结合,导致未知基因的转录激活增加。在此,c-MYC癌基因被确定为该信号通路中的一个靶基因。结果表明,野生型APC可抑制c-MYC的表达,β-连环蛋白可激活c-MYC的表达,且这些效应是通过c-MYC启动子中的Tcf-4结合位点介导的。这些结果为理解结直肠癌中c-MYC此前难以解释的过表达提供了一个分子框架。

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