| Literature DB >> 9727977 |
T C He1, A B Sparks, C Rago, H Hermeking, L Zawel, L T da Costa, P J Morin, B Vogelstein, K W Kinzler.
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.Entities:
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Year: 1998 PMID: 9727977 DOI: 10.1126/science.281.5382.1509
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728