Somatic deletions and mutations of c-Ha-ras gene in human cervical cancers

Oncogene. 1988 Sep;3(3):329-33.

Abstract

The c-Ha-ras-1 locus was analysed in cervical cancers and shown to exhibit the loss of one allele in 36% of heterozygous tumours and a mutation at codon 12 in 24% of tumours at advanced stages. 40% of tumours with mutation contained also a deletion. A c-myc gene activation was found in 100% and 70% of tumours containing mutation and deletion respectively. This suggests that the two proto-oncogenes cooperate for the progression of cervical cancers. Furthermore as more than 90% of these tumours contained also human papillomavirus sequences, our data strongly suggest that multiple genetic events are involved in the genesis and progression of most cervical cancers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Carcinoma, Squamous Cell / genetics*
  • Chromosome Deletion
  • Codon
  • DNA, Neoplasm / analysis
  • Female
  • Heterozygote
  • Humans
  • Mutation
  • Neoplasm Proteins / genetics
  • Proto-Oncogene Proteins / genetics*
  • Proto-Oncogene Proteins c-myc
  • Proto-Oncogene Proteins p21(ras)
  • Proto-Oncogenes*
  • Restriction Mapping
  • Uterine Cervical Neoplasms / genetics*

Substances

  • Codon
  • DNA, Neoplasm
  • Neoplasm Proteins
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-myc
  • HRAS protein, human
  • Proto-Oncogene Proteins p21(ras)