H-ras mutation is an additional event of sarcomatous transformation in aerodigestive spindle cell carcinoma

Oncol Rep. 2004 Mar;11(3):597-604.

Abstract

The conversion from a carcinomatous component to a sarcomatous one in spindle cell carcinoma (SPCC) of the upper aerodigestive tract is thought to occur via a series of molecular alterations; however the detailed mechanism is still unknown. We examined mutations at the H-ras and p53 genes in 16 SPCCs of upper aerodigestive tracts using PCR-RFLP, PCR-SSCP and direct sequencing analysis. The two distinct components, sarcomatous and carcinomatous components in SPCC, were analyzed independently. p53 mutations were detected in both components of SPCC (50.0%, 8/16), and those in the sarcomatous component were completely in accordance with those in the carcinomatous one. In contrast, H-ras mutations were detected only in the sarcomatous component (12.5%, 2/16), and not in the carcinomatous one (0%, 0/16). There was a statistically significant difference in prognosis between the patients with the H-ras mutation (n=2) and those without (n=14); the former had poorer prognosis (P=0.0049). Our results seem to suggest that the H-ras mutation is a relatively uncommon event in SPCC; however, the presence of H-ras mutations may be associated with a more malignant potential in SPCC, while actually occurring during the sarcomatous change itself.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Cell Transformation, Neoplastic*
  • Codon
  • DNA / metabolism
  • DNA Mutational Analysis
  • Female
  • Genes, p53
  • Genes, ras / genetics*
  • Humans
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Mutation*
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Prognosis
  • Respiratory Tract Neoplasms / genetics*
  • Respiratory Tract Neoplasms / mortality
  • Sarcoma / genetics*
  • Sarcoma / mortality
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / mortality
  • Time Factors

Substances

  • Codon
  • DNA