ICI 182,780-Regulated Gene Expression in DU145 Prostate Cancer Cells Is Mediated by Estrogen Receptor-β/NFκB Crosstalk

Neoplasia: An International Journal for Oncology Research

Ying Gao¹  Xiang Zhang¹  Shuk-Mei Ho¹  Yuet-Kin Leung¹  Kin-Mang Lau¹ 

[1]Department of Surgery, University of Massachusetts Medical School, Worcester, MA 01605, USA

关键词: cDNA microarray;    Spi transcription factor;    interleukins;    embryonic growth/differentiation factor (GDF-1);    RYK tyrosine kinase;   

DOI  :  10.1593/neo.05853

来源: DOAJ

【 摘 要 】

Estrogen receptor (ER)-β is the predominant ER subtype in prostate cancer (PCa). We previously demonstrated that ICI 182,780 (ICI), but not estrogens, exerted dose-dependent growth inhibition on DU145 PCa cells by an ER-β-mediated pathway. Transcriptional profiling detected a greater than three-fold upregulation of seven genes after a 12-hour exposure to 1 µM ICI. Semiquantitative reverse transcriptase polymerase chain reaction confirmed the upregulation of four genes by ICI: interleukin-12α chain, interleukin-8, embryonic growthl differentiation factor, and RYK tyrosine kinase. Treatment with an ER-β antisense oligonucleotide reduced cellular ER-β mRNA and induced loss of expression of these genes. Sequence analysis revealed the presence of consensus NFκB sites, but not estrogen-responsive elements, in promoters of all four genes. Reporter assay and chromatin immunoprecipitation experiments demonstrated that ICI-induced gene expression could be mediated by crosstalk between ER-β and the NFκB signaling pathway, denoting a novel mechanism of ERβ-mediated ICI action. Therefore, combined therapies targeting ER-β and NFκB signaling may be synergistic as treatment for PCa.

【 授权许可】

Unknown