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Human α2β1HI CD133+VE Epithelial Prostate Stem Cells Express Low Levels of Active Androgen Receptor

Lookup NU author(s): Dr Stuart Williamson, Dr Anastasia Hepburn, Laura WilsonORCiD, Dr Kelly Coffey, Claudia Ryan-Munden, Dr Deepali Pal, Professor Craig Robson, Professor Rakesh Heer



Stem cells are thought to be the cell of origin in malignant transformation in many tissues, but their role in human prostate carcinogenesis continues to be debated. One of the conflicts with this model is that cancer stem cells have been described to lack androgen receptor (AR) expression, which is of established importance in prostate cancer initiation and progression. We re-examined the expression patterns of AR within adult prostate epithelial differentiation using an optimised sensitive and specific approach examining transcript, protein and AR regulated gene expression. Highly enriched populations were isolated consisting of stem (alpha(2)beta(HI)(1) CD133(+VE)), transiently amplifying (alpha(2)beta(HI)(1) CD133(-VE)) and terminally differentiated (alpha(2)beta(LOW)(1) CD133(-VE)) cells. AR transcript and protein expression was confirmed in alpha(2)beta(HI)(1) CD133(+VE) and CD133(-VE) progenitor cells. Flow cytometry confirmed that median (+/- SD) fraction of cells expressing AR were 77% (+/- 66%) in alpha(2)beta(HI)(1) CD133(+VE) stem cells and 68% (+/- 12%) in alpha(2)beta(HI)(1) CD133(-VE) transiently amplifying cells. However, 3-fold lower levels of total AR protein expression (peak and median immunofluorescence) were present in alpha(2)beta(HI)(1) CD133(+VE) stem cells compared with differentiated cells. This finding was confirmed with dual immunostaining of prostate sections for AR and CD133, which again demonstrated low levels of AR within basal CD133(+VE) cells. Activity of the AR was confirmed in prostate progenitor cells by the expression of low levels of the AR regulated genes PSA, KLK2 and TMPRSS2. The confirmation of AR expression in prostate progenitor cells allows integration of the cancer stem cell theory with the established models of prostate cancer initiation based on a functional AR. Further study of specific AR functions in prostate stem and differentiated cells may highlight novel mechanisms of prostate homeostasis and insights into tumourigenesis.

Publication metadata

Author(s): Williamson SC, Hepburn AC, Wilson L, Coffey K, Ryan-Munden CA, Pal D, Leung HY, Robson CN, Heer R

Publication type: Article

Publication status: Published

Journal: PLoS One

Year: 2012

Volume: 7

Issue: 11

Print publication date: 07/11/2012

Date deposited: 27/02/2013

ISSN (electronic): 1932-6203

Publisher: Public Library of Science


DOI: 10.1371/journal.pone.0048944


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