Expression of fibroblast growth factor-8 in adult rat tissues and human prostate carcinoma cells

J Steroid Biochem Mol Biol. 1996 Feb;57(3-4):173-8. doi: 10.1016/0960-0760(95)00259-6.

Abstract

Androgens are essential for normal prostatic and testicular function. However, paracrine and/or autocrine actions of a number of growth factors have been implicated in the function of these tissues. A recent addition to the fibroblast growth factor family, the so called androgen-induced growth factor (AIGF) or fibroblast growth factor-8 (FGF-8), has been proposed to be under strict androgen regulation and induction in the mouse mammary carcinoma cell line SC3. FGF-8, therefore, may have a local role in the prostate, which is known to be an androgen-responsive organ. This study reports, for the first time, the presence of FGF-8 mRNA in normal adult rat tissues (heart, brain, lung, kidney, testis, prostate and ovary), using an optimised reverse transcription and nested polymerase chain reaction (RT-PCR) procedure, although androgen-dependent FGF-8 expression was not demonstrated in these adult tissues. Consistent with the oncogenic characteristics of FGF-8, the corresponding mRNA was detected in the human prostate tumour cell lines LNCaP and DU145. Because the DU145 cell line is known to be androgen-independent, and the expression of FGF-8 mRNA in cultured LNCaP cells also occurred in the absence of exogenous androgens, it can be concluded that the expression of FGF-8 mRNA in these human cell lines, in the rat prostate and in other rat tissues is not under the regulation of androgens as hitherto proposed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Androgens / physiology
  • Animals
  • Base Sequence
  • Female
  • Fibroblast Growth Factor 8
  • Fibroblast Growth Factors*
  • Gene Expression Regulation*
  • Growth Substances / biosynthesis
  • Growth Substances / genetics*
  • Humans
  • Male
  • Mice
  • Molecular Sequence Data
  • Neoplasm Proteins / biosynthesis
  • Neoplasm Proteins / genetics*
  • Organ Specificity
  • Polymerase Chain Reaction / methods
  • Prostate / metabolism*
  • Prostatic Neoplasms / metabolism*
  • RNA, Messenger / analysis*
  • Rats
  • Rats, Sprague-Dawley
  • Sequence Analysis, DNA
  • Testis / metabolism
  • Tumor Cells, Cultured

Substances

  • Androgens
  • FGF8 protein, human
  • Fgf8 protein, rat
  • Growth Substances
  • Neoplasm Proteins
  • RNA, Messenger
  • Fibroblast Growth Factor 8
  • Fibroblast Growth Factors