Advance in research on the correlation between genotypes of susceptible mutations and clinical phenotype of familial adenomatous polyposis.
10.3760/cma.j.issn.1003-9406.2017.06.031
- Author:
Shengliang HE
1
;
Jing DU
;
Fangqi LIU
Author Information
1. Department of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai 200032, China. Email: 12131230023@fudan.edu.cn.
- Publication Type:Journal Article
- MeSH:
Adenomatous Polyposis Coli;
genetics;
Axin Protein;
genetics;
DNA Glycosylases;
genetics;
Genes, APC;
Genetic Association Studies;
Genetic Predisposition to Disease;
Humans;
Mutation;
beta Catenin;
genetics
- From:
Chinese Journal of Medical Genetics
2017;34(6):919-923
- CountryChina
- Language:Chinese
-
Abstract:
Familial adenomatous polyposis (FAP) is one of the most common hereditary colorectal cancers. Its intestinal and extra-intestinal manifestations are correlated with mutation sties of the APC gene. Potential gene modulation sites in patients who have typical clinical manifestations but with unidentified APC mutations are also discussed, which included MUTYH gene, AXIN gene and certain epigenetic changes. With the generalization of Precision Medicine, to offer individualized treatment and surveillance strategy based on the genotype-phenotype correlation will be of great value for FAP patients. This review focuses on the research advance in genotype - phenotype correlation studies of FAP patients.
