Comparative analysis of epidermal growth factor receptor gene expression and protein product in benign, premalignant, and malignant prostate tissue

Prostate. 1994 Oct;25(4):199-205. doi: 10.1002/pros.2990250405.

Abstract

In order to more clearly define the status of epidermal growth factor receptor (EGFR) in prostate cancer, expression of EGFR transcript and protein was analyzed in paired samples of benign and malignant tissues from 30 radical prostatectomy specimens. Prostate tumors and high grade prostatic intraepithelial neoplasias (PINs) expressed significantly less EGFR protein than benign tissues or low grade PINs (P < 0.001). Expression of EGFR mRNA was analyzed in a subset of the same samples, and was higher in more prostate tumors than benign specimens (P < 0.05). However, differences in mean mRNA expression between malignant and benign tissues were not significant. EGFR mRNA was expressed at moderate or low levels in equivalent numbers of PIN lesions. These results suggest that, although EGFR mRNA expression is somewhat elevated in prostate tumors, EGFR protein expression may be down-regulated in the same malignant tissues. Furthermore, our data demonstrate phenotypic similarity between prostate tumors and high grade PIN at the level of EGFR protein expression.

Publication types

  • Comparative Study

MeSH terms

  • Aged
  • Atrophy
  • Carcinoma in Situ / chemistry
  • Carcinoma in Situ / pathology
  • Epidermal Growth Factor / analysis
  • ErbB Receptors / analysis*
  • ErbB Receptors / genetics
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • Male
  • Middle Aged
  • Precancerous Conditions / pathology*
  • Prostate / chemistry*
  • Prostate / pathology
  • Prostatic Hyperplasia / pathology*
  • Prostatic Neoplasms / chemistry
  • Prostatic Neoplasms / pathology*
  • RNA, Messenger / analysis
  • Transforming Growth Factor alpha / analysis

Substances

  • RNA, Messenger
  • Transforming Growth Factor alpha
  • Epidermal Growth Factor
  • ErbB Receptors