P53 expression, ploidy and progression in pT1 transitional cell carcinoma of the bladder

Br J Urol. 1994 May;73(5):533-7. doi: 10.1111/j.1464-410x.1994.tb07639.x.

Abstract

Objective: To investigate a potential role for overexpression of the p53 protein in the identification of pT1 bladder tumours destined to progress.

Patients and methods: The protein expression of the tumour suppressor gene p53, nuclear ploidy and tumour grade were studied in 25 patients with pT1 bladder tumours. Follow-up data was available for 21 tumours over a 10 year period. p53 expression was determined by immuno-histochemistry on paraffin embedded sections and flow cytometry was performed on cell suspensions derived from the same blocks.

Results: Ten of 21 (48%) tumours progressed to muscle invasive disease. Nuclear staining for the protein was seen in 16 (64%) tumours and of these nine (56%) progressed. All tumours with abnormal DNA content and all high grade tumours demonstrated overexpression of p53. Significantly more patients with high levels of p53 expression (> 10% nuclear staining) progressed compared with tumours with less than 10% of nuclei staining (P = 0.007). However, grade was the most specific predictor of progression (100%), with all grade 3 tumours progressing and grade was also the most significant prognostic indicator in terms of survival (P = 0.025).

Conclusion: Tumour grade is likely to remain as the most useful aid to management decisions in pT1 bladder tumours.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Biomarkers, Tumor / analysis*
  • Carcinoma, Transitional Cell / chemistry*
  • Carcinoma, Transitional Cell / pathology
  • DNA, Neoplasm / analysis
  • Female
  • Follow-Up Studies
  • Humans
  • Immunoenzyme Techniques
  • Male
  • Neoplasm Proteins / analysis*
  • Ploidies
  • Prognosis
  • Tumor Suppressor Protein p53 / analysis*
  • Urinary Bladder Neoplasms / chemistry*
  • Urinary Bladder Neoplasms / pathology

Substances

  • Biomarkers, Tumor
  • DNA, Neoplasm
  • Neoplasm Proteins
  • Tumor Suppressor Protein p53