Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Familial adenomatous polyposis (FAP) is an autosomal dominant inherited disease characterized by the presence of adenomatous polyps in the colon and rectum, with inevitable development of colorectal cancer if left untreated. FAP is caused by germline mutations in the adenomatous polyposis coli (APC) gene. Somatic mutations in the APC gene are an early event in colorectal tumorigenesis, and can be detected in the majority of colorectal tumours. The APC gene encodes a large protein with multiple cellular functions and interactions, including roles in signal transduction in the wnt-signalling pathway, mediation of intercellular adhesion, stabilization of the cytoskeleton and possibly regulation of the cell cycle and apoptosis. The fact that APC is an integral part of so many different pathways makes it an ideal target for mutation in carcinogenesis. This review deals with our understanding to date of how mutations in the APC gene translate into changes at the protein level, which in turn contribute to the role of APC in tumorigenesis.

Type

Journal article

Journal

Hum Mol Genet

Publication Date

04/2001

Volume

10

Pages

721 - 733

Keywords

Adenomatous Polyposis Coli, Adenomatous Polyposis Coli Protein, Apoptosis, Binding Sites, Colorectal Neoplasms, Cytoskeletal Proteins, DNA Methylation, Genotype, Germ-Line Mutation, Humans, Models, Genetic, Mutation, Mutation, Missense, Phenotype, Promoter Regions, Genetic, Protein Structure, Tertiary, Signal Transduction