Absence of microsatellite instability in transitional cell carcinoma of the bladder

Urology. 2000 Feb;55(2):287-91. doi: 10.1016/s0090-4295(99)00399-4.

Abstract

Objectives: To investigate the prevalence of the microsatellite instability related to mismatch repair (MMR) gene defects using a panel of six microsatellite markers, as recommended by a recent workshop on microsatellite instability in colon cancer, because it is still unclear whether abnormalities in DNA MMR genes are involved in transitional cell carcinoma (TCC) of the bladder.

Methods: Three mononucleotide repeats (BAT26, TGFbetaRII, and BAX) were studied in 33 TCC samples and in four bladder cancer cell lines. Three dinucleotide repeats (D2S123, D5S346, and D17S250) were studied in 21 of these 33 TCC samples.

Results: No alteration was detected either in the 33 TCC samples analyzed or in the four bladder cancer cell lines (T24, J82, 647V, and 1207) studied. A difference between normal and tumor DNA was observed in only 1 of 21 tumor samples for D17S250.

Conclusions: These data indicate that microsatellite instability is very uncommon in TCC of the bladder.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Carcinoma, Transitional Cell / genetics*
  • Female
  • Humans
  • Loss of Heterozygosity
  • Male
  • Microsatellite Repeats*
  • Middle Aged
  • Polymerase Chain Reaction
  • Tumor Cells, Cultured
  • Urinary Bladder Neoplasms / genetics*