Modeling the Effect of APC Truncation on Destruction Complex Function in Colorectal Cancer Cells

In colorectal cancer cells, APC, a tumor suppressor protein, is commonly expressed in truncated form. Truncation of APC is believed to disrupt degradation of β—catenin[Image: see text], which is regulated by a multiprotein complex called the destruction complex. The destruction complex comprises APC, Axin, β—catenin[Image: see text], serine/threonine kinases, and other proteins. The kinases [Image: see text] and [Image: see text], which are recruited by Axin, mediate phosphorylation of β—catenin[Image: see text], which initiates its ubiquitination and proteosomal degradation. The mechanism of regulation of β—catenin[Image: see text] degradation by the destruction complex and the role of truncation of APC in colorectal cancer are not entirely understood. Through formulation and analysis of a rule-based computational model, we investigated the regulation of β—catenin[Image: see text] phosphorylation and degradation by APC and the effect of APC truncation on function of the destruction complex. The model integrates available mechanistic knowledge about site-specific interactions and phosphorylation of destruction complex components and is consistent with an array of published data. We find that the phosphorylated truncated form of APC can outcompete Axin for binding to β—catenin[Image: see text], provided that Axin is limiting, and thereby sequester β—catenin[Image: see text] away from Axin and the Axin-recruited kinases [Image: see text] and [Image: see text]. Full-length APC also competes with Axin for binding to β—catenin[Image: see text]; however, full-length APC is able, through its SAMP repeats, which bind Axin and which are missing in truncated oncogenic forms of APC, to bring β—catenin[Image: see text] into indirect association with Axin and Axin-recruited kinases. Because our model indicates that the positive effects of truncated APC on β—catenin[Image: see text] levels depend on phosphorylation of APC, at the first 20-amino acid repeat, and because phosphorylation of this site is mediated by [Image: see text], we suggest that [Image: see text] is a potential target for therapeutic intervention in colorectal cancer. Specific inhibition of [Image: see text] is predicted to limit binding of β—catenin[Image: see text] to truncated APC and thereby to reverse the effect of APC truncation.