Oncogenic activation of androgen receptor

Hsing Jien Kung, Christopher P. Evans

Research output: Contribution to journalReview article

38 Citations (Scopus)

Abstract

Background: There is considerable evidence implicating the aberrant activation or "reactivation" of androgen receptor in the course of androgen-ablation therapy as a potential cause for the development of castration-resistant prostate cancer. Several non-mutually exclusive mechanisms including the inappropriate activation of androgen receptor (AR) by non-steroids have been postulated. The present work is aimed to understand the role of neuropeptides released by neuroendocrine transdifferentiated prostate cancer cells in the aberrant activation of AR. Objectives: The study was designed to study how neuropeptides such as gastrin-releasing peptide activate AR and to define the crucial signal pathways involved, in the hope to identify therapeutic targets. Methods and Materials: Androgen-dependent LNCaP cell line was used to study the effects of bombesin/gastrin-releasing peptide on the growth of the cell line and the transactivation of AR. The neuropeptide was either added to the media or introduced as a transgene in LNCaP cells to study its paracrine or autocrine effect on LNCaP growth under androgen-deprived conditions. The activation of AR was monitored by reporter assay, chromatin immunoprecipitation (ChIP) of AR, translocation into the nucleus and cDNA microarray of the AR response genes. Results: Bombesin/gastrin releasing peptides induce androgen-independent growth of LNCaP in vitro and in vivo. It does so by activating AR, which is accompanied by the activation of Src tyrosine kinase and its target c-myc oncogene. The bombesin or Src-activated AR induces an overlapping set of AR response genes as androgen, but they also a unique set of genes. Intriguingly, the Src-activated and androgen-bound ARs differ in their binding specificity toward AR response elements, indicating the receptors activated by these 2 mechanisms are not conformationally identical. Finally, Src inhibitor was shown to effectively block the activation of AR and the growth effects induced by bombesin. Conclusion: The results showed that AR can be activated by neuropeptide, a ligand for G-protein coupled receptor, in the absence of androgen. The activation goes through Src-tyrosine kinase pathway, and tyrosine kinase inhibitor is a potentially useful adjunctive therapy during androgen ablation.

Original languageEnglish
Pages (from-to)48-52
Number of pages5
JournalUrologic Oncology: Seminars and Original Investigations
Volume27
Issue number1
DOIs
Publication statusPublished - Jan 1 2009
Externally publishedYes

Fingerprint

Androgen Receptors
Androgens
Bombesin
Gastrin-Releasing Peptide
Neuropeptides
src-Family Kinases
Growth
Prostatic Neoplasms
Genes
Cell Line
myc Genes
Chromatin Immunoprecipitation
Castration
Response Elements
G-Protein-Coupled Receptors
Oligonucleotide Array Sequence Analysis
Transgenes
Protein-Tyrosine Kinases
Transcriptional Activation
Signal Transduction

Keywords

  • Androgen receptor activation
  • Hormone refractory prostate cancers
  • Neuroendocrine differentiation
  • Neuropeptides
  • Src tyrosine kinase
  • Tyrosine kinase inhibitor

ASJC Scopus subject areas

  • Oncology
  • Urology

Cite this

Oncogenic activation of androgen receptor. / Kung, Hsing Jien; Evans, Christopher P.

In: Urologic Oncology: Seminars and Original Investigations, Vol. 27, No. 1, 01.01.2009, p. 48-52.

Research output: Contribution to journalReview article

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