Expression of transforming growth factor-beta 1 in human bladder cancer

Cancer. 1995 May 15;75(10):2565-70. doi: 10.1002/1097-0142(19950515)75:10<2565::aid-cncr2820751025>3.0.co;2-m.

Abstract

Background: Elevated expression of transforming growth factor-beta 1 (TGF-beta 1) has been reported in several types of human cancer. However, the significance of TGF-beta 1 expression in clinical bladder cancer is not well known.

Methods: The levels of TGF-beta 1 expression were quantitated using a polymerase chain reaction-based method in tissue specimens obtained from 51 patients with bladder cancer.

Results: Transforming growth factor-beta 1 expression in bladder cancer was higher than that found in normal bladder epithelium (P < 0.01). Significantly higher levels of TGF-beta 1 transcripts were observed in low and intermediate grade (Grade 1 and 2) tumors than in high grade (Grade 3) tumors (P < 0.02). Superficial (pTa and pT1) tumors had higher levels of TGF-beta 1 than invasive (pT2 or higher) tumors (P < 0.05).

Conclusions: These results suggest that enhanced expression of TGF-beta 1 is specific to low grade and stage bladder cancer. Transforming growth factor-beta 1 may play an important role in the early stages of human bladder cancer development, and TGF-beta 1 expression could provide a new relevant tumor marker for determining tumor progression in patients with bladder cancer.

MeSH terms

  • Actins / genetics
  • Actins / metabolism
  • Aged
  • Carcinoma, Squamous Cell / genetics
  • Carcinoma, Squamous Cell / metabolism
  • Carcinoma, Squamous Cell / pathology
  • Carcinoma, Transitional Cell / genetics*
  • Carcinoma, Transitional Cell / metabolism
  • Carcinoma, Transitional Cell / pathology
  • Epithelium / metabolism
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Lymphotoxin-alpha / genetics*
  • Lymphotoxin-alpha / metabolism
  • Male
  • Neoplasm Invasiveness
  • Neoplasm Recurrence, Local / genetics
  • Neoplasm Recurrence, Local / metabolism
  • Neoplasm Recurrence, Local / pathology
  • Neoplasm Staging
  • Polymerase Chain Reaction
  • RNA, Neoplasm / genetics
  • RNA, Neoplasm / metabolism
  • Transcription, Genetic
  • Tumor Cells, Cultured
  • Urinary Bladder / metabolism
  • Urinary Bladder Neoplasms / genetics*
  • Urinary Bladder Neoplasms / metabolism
  • Urinary Bladder Neoplasms / pathology

Substances

  • Actins
  • Lymphotoxin-alpha
  • RNA, Neoplasm