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Microarray coupled to quantitative RT-PCR analysis of androgen-regulated genes in human LNCaP prostate cancer cells.

Abstract
The androgen receptor (AR) mediates the growth-stimulatory effects of androgens in prostate cancer cells. Identification of androgen-regulated genes in prostate cancer cells is therefore of considerable importance for defining the mechanisms of prostate-cancer development and progression. Although several studies have used microarrays to identify AR-regulated genes in prostate cancer cell lines and in prostate tumours, we present here the results of gene expression microarray profiling of the androgen-responsive LNCaP prostate-cancer cell line treated with R1881 for the identification of androgen-regulated genes. We show that the expression of 319 genes is stimulated by 24 h after R1881 addition, with a similar number (300) of genes being significantly repressed. Expression of the upregulated genes, as well as of 60 of the most robustly downregulated genes, was carried out using quantitative RT-PCR (Q-RT-PCR) over a time-course of R1881 treatment from 0 to 72 h. Q-RT-PCR was also carried out following treatment with other AR agonists (dihydrotestosterone, estradiol and medroxyprogesterone) and antagonists (cyproterone acetate, hydroxyflutamide and bicalutamide). This study provides a comprehensive analysis of androgen-regulated gene expression in the LNCaP prostate cancer cell line, and identifies a number of androgen-regulated genes, not described previously, as candidates for mediating androgen responses in prostate cancer cells.
AuthorsS Ngan, E A Stronach, A Photiou, J Waxman, S Ali, L Buluwela
JournalOncogene (Oncogene) Vol. 28 Issue 19 Pg. 2051-63 (May 14 2009) ISSN: 1476-5594 [Electronic] England
PMID19363526 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • AR protein, human
  • Androgens
  • Receptors, Androgen
  • Metribolone
Topics
  • Androgens (metabolism)
  • Cell Line, Tumor
  • Gene Expression Profiling
  • Humans
  • Male
  • Metribolone (pharmacology)
  • Oligonucleotide Array Sequence Analysis
  • Prostatic Neoplasms (metabolism)
  • Receptors, Androgen (genetics)
  • Reverse Transcriptase Polymerase Chain Reaction

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