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Characterization of the androgen receptor in a benign prostate tissue-derived human prostate epithelial cell line: RC-165N/human telomerase reverse transcriptase.

Authors :
Kim, K.-H.
Dobi, A.
Shaheduzzaman, S.
Gao, C. L.
Masuda, K.
Li, H.
Drukier, A.
Gu, Y.
Srikantan, V.
Rhim, J. S.
Srivastava, S.
Source :
Prostate Cancer & Prostatic Diseases. 2007, Vol. 10 Issue 1, p30-38. 9p. 2 Charts, 4 Graphs.
Publication Year :
2007

Abstract

The majority of prostate epithelial cell lines stably expressing wild-type (wt) or mutant (mt) androgen receptor (AR) are derived from metastatic prostate cancers. Therefore, the wt AR-expressing RC-165N/human telomerase reverse transcriptase (hTERT) cell line derived from the benign prostate tissue of an African-American patient provides a unique opportunity to assess the functional status of AR in a cellular context not studied before. Although androgen-induced expression of known androgen responsive genes such as PMEPA1, and NDRG1 was observed in RC-165N/hTERT, this cell line expresses prostate-specific antigen (PSA) at significantly lower levels. Chromatin immunoprecipitation assay revealed androgen-dependent binding of AR to androgen response elements of PSA, PMEPA1 and NDRG1 genes. Similarities, as well as differences were noted in the expression of androgen responsive genes between RC-165N/hTERT and LNCaP cells. Comprehensive evaluations of AR functions in RC-165N/hTERT cells suggest that whereas some features of known AR functions are maintained in this benign prostatic tissue-derived cell line, other AR functions are not retained. Objective evaluations of similar cell lines will lead to the understanding of AR functions in prostate growth and differentiation.Prostate Cancer and Prostatic Diseases (2007) 10, 30–38. doi:10.1038/sj.pcan.4500915; published online 31 October 2006 [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13657852
Volume :
10
Issue :
1
Database :
Academic Search Index
Journal :
Prostate Cancer & Prostatic Diseases
Publication Type :
Academic Journal
Accession number :
24197707
Full Text :
https://doi.org/10.1038/sj.pcan.4500915