K-ras mutation, HPV infection and smoking or alcohol abuse positively correlate with esophageal squamous carcinoma

Pathol Oncol Res. 2008 Sep;14(3):267-73. doi: 10.1007/s12253-008-9032-1. Epub 2008 Jul 1.

Abstract

The Ras/Raf/MEK/ERK (MAPK) signal transduction cascade is an important mediator of a number of cellular fates including growth, survival and apoptosis. The aim of this study was to determine the incidence of B-raf, Kirsten-ras (K-ras) and Neuroblastoma-ras (N-ras) gene mutations in esophageal squamous cell carcinoma (ESCC) in the Greek population. DNA was extracted from 30 ESCC and 32 normal esophageal specimens and screened for V600E B-raf, and K-ras/N-ras codon 12 mutations, by PCR-RFLP based analysis. Among the genes tested, only the heterozygous K-ras mutation was detected in 5 out of the 30 ESCC specimens (16%), whereas no mutation was found in the normal esophageal tissue (P < 0.022). The normal samples were screened negative for N-ras and V600E B-raf mutations. The increased risk of esophageal cancer was correlated with tobacco use (OR = 3.5, P < 0.023) and alcohol abuse (OR = 7.22, P < 0.001), accompanied with the high incidence of the k-ras codon 12 mutation (22%, OR = 1.77 and 21%, OR = 1.52), respectively. A similar positive association was seen in human papilloma virus (HPV)-infected patients (OR = 5.66, P < 0.003). Our overall findings demonstrate that the mutational activation of the K-ras gene, HPV infection and tobacco or alcohol abuse, can be considered independently or in combination as high risk factors for ESCC development.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alcoholism*
  • Carcinoma, Squamous Cell / epidemiology
  • Carcinoma, Squamous Cell / ethnology
  • Carcinoma, Squamous Cell / genetics
  • Case-Control Studies
  • Esophageal Neoplasms / epidemiology*
  • Esophageal Neoplasms / ethnology
  • Esophageal Neoplasms / genetics*
  • Female
  • Genes, ras / genetics*
  • Greece
  • Humans
  • Male
  • Mediterranean Region
  • Middle Aged
  • Mutation / genetics*
  • Papillomavirus Infections*
  • Proto-Oncogene Proteins B-raf / genetics
  • Retrospective Studies
  • Risk Factors
  • Smoking*

Substances

  • Proto-Oncogene Proteins B-raf