Androgen-induced expression of endoplasmic reticulum (ER) stress response genes in prostate cancer cells.

Published

Journal Article

Evaluations of androgen regulated gene (ARG) repertoire provide new insights into the androgen receptor (AR) mediated signaling at the transcriptional level. Definition of ARGs having critical functions in the biology of normal and malignant prostate should aid in identifying new bio-markers and therapeutic targets for prostate cancer (CaP). Using Affymetrix HuGene FL oligonucleotide arrays, temporal expression profiles of ARGs in widely used hormone responsive LNCaP cells, were analysed by hierarchical clustering methods and functional classification. ARGs in response to different androgen concentrations showed temporal co-regulation of genes involved in specific biochemical pathways. This study focuses on our new observations of the coordinated androgen induction of genes (NDRG1, PDIR, HERPUD1, ORP150) involved in the endoplasmic reticulum (ER) stress response pathway. Expression analysis of the two selected ER stress responsive genes, NDRG1 and HERPUD1 in primary CaPs revealed a significantly reduced tumor associated expression. Intriguing linkage of the androgen signaling to ER stress responsive genes, a protective response to protein unfolding or protein damage resulting from cellular stress signals, suggests that androgens may induce such stress signals in CaP cells. Decreased CaP associated expression of two ER stress responsive genes also suggests that possible abrogation of this pathway in prostate tumorigenesis.

Full Text

Duke Authors

Cited Authors

  • Segawa, T; Nau, ME; Xu, LL; Chilukuri, RN; Makarem, M; Zhang, W; Petrovics, G; Sesterhenn, IA; McLeod, DG; Moul, JW; Vahey, M; Srivastava, S

Published Date

  • December 2002

Published In

Volume / Issue

  • 21 / 57

Start / End Page

  • 8749 - 8758

PubMed ID

  • 12483528

Pubmed Central ID

  • 12483528

Electronic International Standard Serial Number (EISSN)

  • 1476-5594

International Standard Serial Number (ISSN)

  • 0950-9232

Digital Object Identifier (DOI)

  • 10.1038/sj.onc.1205992

Language

  • eng