MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps

Gastroenterology. 2004 Jul;127(1):9-16. doi: 10.1053/j.gastro.2004.03.070.

Abstract

Background & aims: MYH-associated polyposis is a recently described disease that is characterized by multiple colorectal adenomas and a recessive pattern of inheritance. Individuals with MYH-associated polyposis have biallelic mutations in MYH, a base excision repair gene, and are negative for germline mutations in the APC gene. In this study, the 2 most prevalent MYH mutations in white persons, Y165C and G382D, were analyzed for their presence in 984 subjects selected from 3 groups: 400 undergoing screening colonoscopy and found to have 0-3 polyps, 444 with colorectal cancer (CRC), and 140 referred for APC mutation analysis in which a germline mutation was not identified.

Methods: Genotyping for Y165C and G382D was performed by Pyrosequencing.

Results: Biallelic mutations for Y165C and/or G382D were not found in any of those undergoing screening colonoscopy with 0-3 polyps (n = 400), in those APC-negative patients with <20 adenomatous polyps (n = 26), or in those with CRC who were older than 50 years (n = 328). Furthermore, these 2 MYH mutations were not found among patients whose tumors showed the presence of defective DNA mismatch repair (n = 62). However, the presence of biallelic germline MYH mutations correlated with the presence of >or=20 adenomatous polyps. Interestingly, 2 of the 116 individuals with CRC diagnosed at 50 years of age or younger also presented with biallelic germline mutations in MYH.

Conclusions: These data suggest that screening of MYH should be considered not only in patients with multiple polyps but also in patients with early-onset CRC.

MeSH terms

  • Adenomatous Polyposis Coli / genetics*
  • Adult
  • Aged
  • Colorectal Neoplasms, Hereditary Nonpolyposis / genetics*
  • DNA Glycosylases / genetics*
  • Genes, APC / physiology
  • Genetic Predisposition to Disease
  • Genotype
  • Germ-Line Mutation / genetics
  • Humans
  • Middle Aged
  • Sequence Analysis, DNA

Substances

  • DNA Glycosylases
  • mutY adenine glycosylase