Testosterone-repressed prostate message-2 is an antiapoptotic gene involved in progression to androgen independence in prostate cancer

Cancer Res. 2000 Jan 1;60(1):170-6.

Abstract

Although initially reported as an androgen-repressed gene in the rat prostate, the functional role of testosterone-repressed prostate message-2 (TRPM-2) in apoptosis remains undefined. Inhibition of castration-induced apoptosis by calcium channel blocker treatment in androgen-dependent Shionogi tumors resulted in the prevention of TRPM-2 gene up-regulation, suggesting that TRPM-2 is not directly androgen-repressed, but is regulated by apoptotic stimuli. The overexpression of the TRPM-2 gene in human androgen-dependent LNCaP prostate cancer cells by stable transfection rendered them highly resistant to androgen ablation in vivo. We then tested the efficacy of antisense TRPM-2 oligodeoxynucleotide (ODN) therapy in the Shionogi tumor model and demonstrated that the systemic administration of antisense TRPM-2 ODNs in mice bearing Shionogi tumors after castration resulted in a more rapid onset of apoptosis and time to complete regression, as well as a significant delay of emergence of androgen-independent recurrent tumors compared to control ODN treatment. Collectively, these findings illustrate that TRPM-2 is an antiapoptotic rather than an androgen-repressed gene that confers resistance to androgen ablation and thereby helps accelerate the progression to androgen independence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Blotting, Northern
  • Blotting, Western
  • Calcium Channel Blockers / pharmacology
  • Clusterin
  • Disease Progression
  • Genetic Vectors
  • Glycoproteins / drug effects
  • Glycoproteins / genetics
  • Glycoproteins / metabolism*
  • Humans
  • In Situ Nick-End Labeling
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Molecular Chaperones*
  • Neoplasm Proteins / drug effects
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism*
  • Neoplasms, Hormone-Dependent / metabolism
  • Oligodeoxyribonucleotides, Antisense
  • Orchiectomy
  • Prostatic Neoplasms / metabolism*
  • RNA, Messenger / metabolism
  • Up-Regulation / drug effects

Substances

  • CLU protein, human
  • Calcium Channel Blockers
  • Clu protein, mouse
  • Clusterin
  • Glycoproteins
  • Molecular Chaperones
  • Neoplasm Proteins
  • Oligodeoxyribonucleotides, Antisense
  • RNA, Messenger