[Loss of heterozygosity in the 9p21 region as an inactivation mechanism of the p16 suppressor gene]

Arch Esp Urol. 2000 Sep;53(7):603-9.
[Article in Spanish]

Abstract

Objective: To determine the loss of heterozygosity (LOH) on 9p21 (locus D9S1747) in patients with renal carcinoma by analysis of microsatellite polymorphisms.

Methods: 40 patients with sporadic renal cancer were studied. LOH on 9p21 was performed by analysis of microsatellite polymorphisms.

Results: 23.7% showed LOH on 9p21. No correlation was found between this genetic alteration and tumor features.

Conclusions: LOH on 9p21 was found in 23.7% of the patients in this series. LOH was found in 26.9% of renal cell carcinomas, 25% of papillary carcinomas and 25% of Bellini duct carcinomas. LOH was not found in the other histological types.

Publication types

  • English Abstract

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Carcinoma, Papillary / genetics*
  • Carcinoma, Renal Cell / genetics*
  • Chromosomes, Human, Pair 9 / genetics*
  • Female
  • Genes, p16 / genetics*
  • Humans
  • Kidney Neoplasms / genetics*
  • Loss of Heterozygosity*
  • Male
  • Microsatellite Repeats
  • Middle Aged
  • Polymorphism, Genetic