Direct molecular analysis of a deletion of 3p in tumors from patients with sporadic renal cell carcinoma

Cancer Genet Cytogenet. 1988 Jun;32(2):281-5. doi: 10.1016/0165-4608(88)90292-0.

Abstract

Normal and tumorous nephrectomy specimens from seven renal cell carcinoma patients were subjected to a Southern analysis using chromosome #3-specific polymorphic probes. Three patients were not informative because of homozygosity at all loci studied. One patient showing heterozygosity at 3q in normal tissue had a tumor that remained heterozygous. In three patients the tumor showed loss of heterozygosity for a short arm market at 3p21. In one of them heterozygosity for a second short arm marker was also lost. Another of these three patients retained heterozygosity for this second short arm marker, as well as for a long arm marker, suggesting a chromosomal breakpoint between the loci for the two short arm markers. Our results demonstrate that the known involvement of a short arm region of chromosome #3 in the development of renal cell carcinoma can readily be further evaluated by direct molecular methods.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Carcinoma, Renal Cell / genetics*
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 3*
  • DNA Restriction Enzymes
  • DNA, Neoplasm / genetics
  • Deoxyribonuclease HindIII
  • Genetic Markers
  • Heterozygote
  • Humans
  • Kidney Neoplasms / genetics*
  • Nucleic Acid Hybridization

Substances

  • DNA, Neoplasm
  • Genetic Markers
  • DNA Restriction Enzymes
  • Deoxyribonuclease HindIII