Prognostic value of ERG oncoprotein in prostate cancer recurrence and cause‐specific mortality. Issue 9 (17th January 2013)
- Record Type:
- Journal Article
- Title:
- Prognostic value of ERG oncoprotein in prostate cancer recurrence and cause‐specific mortality. Issue 9 (17th January 2013)
- Main Title:
- Prognostic value of ERG oncoprotein in prostate cancer recurrence and cause‐specific mortality
- Authors:
- Spencer, E. Sophie
Johnston, Richard B.
Gordon, Ryan R.
Lucas, Jared M.
Ussakli, Cigdem Himmetoglu
Hurtado‐Coll, Antonio
Srivastava, Shiv
Nelson, Peter S.
Porter, Christopher R. - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="abs1-1" sec-type="section"> <title>BACKGROUND</title> <p>ETS‐related gene (ERG) protein is present in 40–70% of prostate cancer and is correlated with TMPRSS2‐ERG gene rearrangements. This study evaluated ERG expression at radical prostatectomy to determine whether it was predictive of earlier relapse or prostate cancer‐specific mortality (PCSM).</p> </sec> <sec id="abs1-2" sec-type="section"> <title>METHODS</title> <p>One hundred patients who underwent radical prostatectomy at Virginia Mason in Seattle between 1991 and 1997 were identified. Recurrence was confirmed by tissue diagnosis or radiographic signs. PCSM was confirmed by death certificates. Thirty‐three patients with metastases or PCSM were matched to patients without recurrence at a 1:2 ratio. Paraffin embedded tissue was stained with two anti‐ERG monoclonal antibodies, EPR3864 and 9FY. Nuclear expression intensity was evaluated as present/absent, on a 4‐point relative intensity scale, and as a composite score (0–300).</p> </sec> <sec id="abs1-3" sec-type="section"> <title>RESULTS</title> <p>Mean follow‐up was 10.26 years. The two antibodies were highly correlated (<italic>P</italic> &lt; 0.0001). Patients with higher ERG expression intensity and composite scores were significantly more likely to develop biochemical relapse, metastases, and PCSM. Kaplan–Meier survival curve analysis for the composite score of ERG expression revealed a<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="abs1-1" sec-type="section"> <title>BACKGROUND</title> <p>ETS‐related gene (ERG) protein is present in 40–70% of prostate cancer and is correlated with TMPRSS2‐ERG gene rearrangements. This study evaluated ERG expression at radical prostatectomy to determine whether it was predictive of earlier relapse or prostate cancer‐specific mortality (PCSM).</p> </sec> <sec id="abs1-2" sec-type="section"> <title>METHODS</title> <p>One hundred patients who underwent radical prostatectomy at Virginia Mason in Seattle between 1991 and 1997 were identified. Recurrence was confirmed by tissue diagnosis or radiographic signs. PCSM was confirmed by death certificates. Thirty‐three patients with metastases or PCSM were matched to patients without recurrence at a 1:2 ratio. Paraffin embedded tissue was stained with two anti‐ERG monoclonal antibodies, EPR3864 and 9FY. Nuclear expression intensity was evaluated as present/absent, on a 4‐point relative intensity scale, and as a composite score (0–300).</p> </sec> <sec id="abs1-3" sec-type="section"> <title>RESULTS</title> <p>Mean follow‐up was 10.26 years. The two antibodies were highly correlated (<italic>P</italic> &lt; 0.0001). Patients with higher ERG expression intensity and composite scores were significantly more likely to develop biochemical relapse, metastases, and PCSM. Kaplan–Meier survival curve analysis for the composite score of ERG expression revealed a significant association between higher ERG expression (EPR3864) and shorter PCa‐specific survival (<italic>P</italic> = 0.047).</p> </sec> <sec id="abs1-4" sec-type="section"> <title>CONCLUSIONS</title> <p>While the presence of ERG expression at the time of surgery was not predictive of earlier relapse or PCSM, the relative intensity and composite score for ERG expression was prognostic for the development of biochemical relapse, metastases, and PCSM. Quantitative ERG scoring may be useful to identify patients who would benefit from adjuvant treatment or closer follow‐up, allowing more accurate individual patient treatment plans. Prostate 73: 905–912, 2013. © 2013 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Prostate. Volume 73:Issue 9(2013)
- Journal:
- Prostate
- Issue:
- Volume 73:Issue 9(2013)
- Issue Display:
- Volume 73, Issue 9 (2013)
- Year:
- 2013
- Volume:
- 73
- Issue:
- 9
- Issue Sort Value:
- 2013-0073-0009-0000
- Page Start:
- 905
- Page End:
- 912
- Publication Date:
- 2013-01-17
- 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.22636 ↗
- 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:
- 3117.xml