Metallothionein isoform 3 expression in the human prostate and cancer-derived cell lines

Prostate. 1999 Nov 1;41(3):196-202. doi: 10.1002/(sici)1097-0045(19991101)41:3<196::aid-pros7>3.0.co;2-u.

Abstract

Background: Expression of metallothionein isoform 3 (MT-3) was initially reported to be confined to neural tissues. However, it was recently demonstrated that MT-3 is expressed in epithelial cells of the human kidney. This motivated the current examination of the expression of MT-3 in the human prostate.

Methods: Immunohistochemistry (IHC) was used to localize the expression of MT-3, RT-PCR to determine the expression of MT-3 mRNA, and Western blot analysis to determine the level of MT-3 protein.

Results: Selected epithelial and stromal cells of the normal human prostate were shown to have low levels of MT-3 expression. MT-3 was increased in prostatic intraepithelial neoplasia (PIN) lesions and further increased in a highly variable fashion in prostatic adenocarcinoma. In some adenocarcinomas, MT-3 expression exceeded that of nerve. Three cell culture models of prostate cancer were also shown to variably express MT-3. Restriction enzyme analysis confirmed the expression of MT-3 in the cells and tissues.

Conclusions: MT-3 is expressed in the normal human prostate, and expression is enhanced and highly variable in PIN lesions and primary prostate cancer cells. The variable nature of MT-3 expression was also noted in commonly utilized prostate cancer cell lines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Epithelial Cells / physiology
  • Gene Expression Regulation, Neoplastic*
  • Growth Inhibitors / biosynthesis*
  • Growth Inhibitors / genetics
  • Humans
  • Immunohistochemistry
  • Male
  • Metallothionein 3
  • Molecular Sequence Data
  • Nerve Tissue Proteins / biosynthesis*
  • Nerve Tissue Proteins / genetics
  • Prostatic Neoplasms / genetics*
  • RNA, Messenger / analysis
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Cells, Cultured

Substances

  • Growth Inhibitors
  • Metallothionein 3
  • Nerve Tissue Proteins
  • RNA, Messenger