Low somatic K-ras mutation frequency in colorectal cancer diagnosed under the age of 45 years

Eur J Cancer. 2006 Jul;42(10):1357-61. doi: 10.1016/j.ejca.2006.02.023. Epub 2006 Jun 9.

Abstract

Somatic mutation of K-ras is known to be a common event in colorectal cancer tumourigenesis however its association with age at onset has not been widely explored. In this study, we have analyzed tumours from a population-based study of colorectal cancer diagnosed before the age of 45 years, in which cases had been previously screened for germ-line mismatch repair gene mutations and for microsatellite instability. We used a micro-dissection and sequencing approach to search for somatic K-ras mutations in codons 12, 13 and 61 in 101 early-onset colorectal cancers. Six (6%) somatic K-ras mutations were detected; five in codon 12 (4 G>T transitions and 1 G>A) and one in codon 13 (G>A transition). All codon 12 mutations were identified in microsatellite stable tumours and the codon 13 mutation was identified in a MSI-high tumour. Four cases with K-ras mutations had no reported family history of colorectal cancer and two had some family history of colorectal cancer. None were known to carry a germ-line mutation in hMSH2, hMLH1, hMSH6 or hPMS2. The role of somatic K-ras mutations in early-onset colorectal cancer carcinogenesis appears to be minor, in contrast to its significant role in colorectal cancer of later age of onset.

MeSH terms

  • Adult
  • Age Factors
  • Colorectal Neoplasms / genetics*
  • Female
  • Genes, ras / genetics*
  • Humans
  • Immunohistochemistry
  • Male
  • Microsatellite Repeats
  • Mutation / genetics*