Abstract
The androgen receptor (AR) is central to the initiation and progression of prostate cancer, even after castration. Its transcriptional activity has previously been studied in cell lines. A group at the University of Cambridge recently outlined the AR transcriptional program in tissue samples, with an emphasis on castration-resistant tumors. AR binding sites, gene-expression changes (in xenografts), and potential transcription factor interactions were notably different from those observed in cultured cells. These discrepancies suggest a distinct signaling network for the AR in vivo and serve as a reminder that results from in vitro models should be checked against clinical realities.
| Original language | English |
|---|---|
| Pages (from-to) | 16-18 |
| Number of pages | 3 |
| Journal | Cancer Biology and Therapy |
| Volume | 15 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jan 2014 |
Keywords
- Androgen receptor
- Binding site
- Castrationresistant prostate cancer
- Transcription factor
- Transcriptional program