The analysis of serum response factor expression in bone and soft tissue prostate cancer metastases. Issue 3 (February 2014)
- Record Type:
- Journal Article
- Title:
- The analysis of serum response factor expression in bone and soft tissue prostate cancer metastases. Issue 3 (February 2014)
- Main Title:
- The analysis of serum response factor expression in bone and soft tissue prostate cancer metastases
- Authors:
- O'Hurley, Gillian
Prencipe, Maria
Lundon, Dara
O'Neill, Amanda
Boyce, Susie
O'Grady, Anthony
Gallagher, William M.
Morrissey, Colm
Kay, Elaine W.
Watson, R. William G. - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="pros22752-sec-0001" sec-type="section"> <title>BACKGROUND</title> <p>Castration‐resistant prostate cancer (CRPC) represents a challenge to treat with no effective treatment options available. We recently identified serum response factor (SRF) as a key transcription factor in an in vitro model of castration resistance where we showed that SRF inhibition resulted in reduced cellular proliferation. We also demonstrated an association between SRF protein expression and CRPC in a cohort of castrate‐resistant transurethral resections of the prostate (TURPS). The mechanisms regulating the growth of CRPC bone and visceral metastases have not been explored in depth due to the paucity of patient‐related material available for analysis. In this study, we aim to evaluate SRF protein expression in prostate cancer (PCa) metastases, which has not previously been reported.</p> </sec> <sec id="pros22752-sec-0002" sec-type="section"> <title>METHODS AND RESULTS</title> <p>We evaluated the nuclear tissue expression profile of SRF by immunohistochemistry in 151 metastatic sites from 42 patients who died of advanced PCa. No relationship between SRF nuclear expression and the site of metastasis was observed (<italic>P</italic> = 0.824). However, a negative association between SRF nuclear expression in bone metastases and survival from (a) diagnosis with PCa (<italic>P</italic> = 0.005) and (b) diagnosis with CRPC<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="pros22752-sec-0001" sec-type="section"> <title>BACKGROUND</title> <p>Castration‐resistant prostate cancer (CRPC) represents a challenge to treat with no effective treatment options available. We recently identified serum response factor (SRF) as a key transcription factor in an in vitro model of castration resistance where we showed that SRF inhibition resulted in reduced cellular proliferation. We also demonstrated an association between SRF protein expression and CRPC in a cohort of castrate‐resistant transurethral resections of the prostate (TURPS). The mechanisms regulating the growth of CRPC bone and visceral metastases have not been explored in depth due to the paucity of patient‐related material available for analysis. In this study, we aim to evaluate SRF protein expression in prostate cancer (PCa) metastases, which has not previously been reported.</p> </sec> <sec id="pros22752-sec-0002" sec-type="section"> <title>METHODS AND RESULTS</title> <p>We evaluated the nuclear tissue expression profile of SRF by immunohistochemistry in 151 metastatic sites from 42 patients who died of advanced PCa. No relationship between SRF nuclear expression and the site of metastasis was observed (<italic>P</italic> = 0.824). However, a negative association between SRF nuclear expression in bone metastases and survival from (a) diagnosis with PCa (<italic>P</italic> = 0.005) and (b) diagnosis with CRPC (<italic>P</italic> = 0.029) was seen. These results demonstrate that SRF nuclear expression in bone metastases is associated with survival, with patients with the shortest survival showing high SRF nuclear expression and patients with the longest survival having low SRF nuclear expression.</p> </sec> <sec id="pros22752-sec-0003" sec-type="section"> <title>CONCLUSION</title> <p>Our study indicates that SRF is a key factor determining patients' survival in metastatic CRPC and therefore may represent a promising target for future therapies. <italic>Prostate 74:306–313, 2014</italic>. © 2013 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Prostate. Volume 74:Issue 3(2014)
- Journal:
- Prostate
- Issue:
- Volume 74:Issue 3(2014)
- Issue Display:
- Volume 74, Issue 3 (2014)
- Year:
- 2014
- Volume:
- 74
- Issue:
- 3
- Issue Sort Value:
- 2014-0074-0003-0000
- Page Start:
- 306
- Page End:
- 313
- Publication Date:
- 2014-02
- Subjects:
- Prostate -- Diseases -- Periodicals
616 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-0045 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pros.22752 ↗
- Languages:
- English
- ISSNs:
- 0270-4137
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6935.194000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3077.xml