Identification of somatic mutations of the RNF6 gene in human esophageal squamous cell carcinoma

Cancer Res. 2002 Aug 1;62(15):4191-3.

Abstract

We mapped a tumor suppressor gene locus to an 800-kb interval on human chromosome 13q12.11 for esophageal squamous cell carcinoma (ESCC). Two genes, ML-1 and RNF6, are located within this 800-kb interval. We analyzed both genes for the presence of mutations in 24 ESCC primary tumors and 16 tumor cell lines by directly sequencing the PCR products that were amplified from each exon. No mutation was detected in ML-1. In contrast, three somatic mutations in the RNF6 gene were detected in the ESCC primary tumors, and one mutation was also found in a tumor cell line. Identification of multiple somatic mutations in RNF6 suggests that RNF6 is a potential tumor suppressor gene involved in the pathogenesis of ESCC.

MeSH terms

  • Carcinoma, Squamous Cell / genetics*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 13 / genetics
  • Cytokines / genetics
  • DNA Mutational Analysis
  • DNA-Binding Proteins / genetics*
  • Esophageal Neoplasms / genetics*
  • Genes, Tumor Suppressor
  • Humans
  • Interleukin-17*
  • Mutation*
  • Tumor Cells, Cultured

Substances

  • Cytokines
  • DNA-Binding Proteins
  • IL17F protein, human
  • Interleukin-17
  • RNF6 protein, human