C-erbB-2 in bladder cancer: molecular biology, correlation with epidermal growth factor receptors and prognostic value

J Urol. 1996 Jan;155(1):321-6. doi: 10.1016/s0022-5347(01)66653-9.

Abstract

Purpose: To study the c-erbB-2 oncogene in primary transitional cell bladder cancer.

Materials and methods: Ninety-five patients with known clinical follow-up and epidermal growth factor receptor (EGFr) status were studied for expression of c-erbB-2 by immunostaining. Possible mechanisms underlying increased staining for c-erbB-2 protein were investigated by analyzing DNA and RNA encoding c-erbB-2.

Results: Strong positive staining for c-erbB-2 was detected in 20 (21%) tumors, with weaker staining in a further 13 (14%). There was no correlation between increased staining for c-erbB-2 and tumor stage, grade, or EGFr status. There was a low rate of amplification of the c-erbB-2 gene (1 of 24) on Southern blotting with a higher rate of elevated c-erbB-2 mRNA (4 of 44) with dot blot hybridization. For pT1 tumors, the rate of recurrence was higher for those tumors which were positive for c-erbB-2.

Conclusions: c-erbB-2 oncoprotein is expressed by a significant proportion of transitional cell tumors of the bladder. In this study, the prognostic significance of c-erbB-2 expression appears limited.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Southern
  • Carcinoma, Transitional Cell / chemistry
  • Carcinoma, Transitional Cell / genetics*
  • Carcinoma, Transitional Cell / mortality
  • DNA, Neoplasm / genetics
  • ErbB Receptors / analysis*
  • Gene Expression
  • Genes, erbB-2*
  • Humans
  • Immunoblotting
  • Neoplasm Recurrence, Local / genetics*
  • Oncogene Proteins v-erbB / biosynthesis*
  • Oncogene Proteins v-erbB / genetics
  • Prognosis
  • RNA, Messenger / genetics
  • RNA, Neoplasm / genetics
  • Urinary Bladder / chemistry
  • Urinary Bladder Neoplasms / chemistry
  • Urinary Bladder Neoplasms / genetics*
  • Urinary Bladder Neoplasms / mortality

Substances

  • DNA, Neoplasm
  • Oncogene Proteins v-erbB
  • RNA, Messenger
  • RNA, Neoplasm
  • ErbB Receptors