Ebp1 expression in benign and malignant prostate

<p>Abstract</p> <p>Background</p> <p>ErbB3-binding protein 1 (Ebp1) is a member of the <it>PA2G4 </it>family of proliferation-regulated proteins that is expressed in multiple malignant and non-malignant cells. ErbB3 and other members of the EGFR family have...

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Main Authors: Mes-Masson Anne-Marie, Karakiewicz Pierre I, Le Page Cécile, Koumakpayi Ismaël, Gannon Philippe O, Saad Fred
Format: Article
Language:English
Published: BMC 2008-11-01
Series:Cancer Cell International
Online Access:http://www.cancerci.com/content/8/1/18
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spelling doaj-405682459b604cb28049ca39ef16dddd2020-11-25T00:43:22ZengBMCCancer Cell International1475-28672008-11-01811810.1186/1475-2867-8-18Ebp1 expression in benign and malignant prostateMes-Masson Anne-MarieKarakiewicz Pierre ILe Page CécileKoumakpayi IsmaëlGannon Philippe OSaad Fred<p>Abstract</p> <p>Background</p> <p>ErbB3-binding protein 1 (Ebp1) is a member of the <it>PA2G4 </it>family of proliferation-regulated proteins that is expressed in multiple malignant and non-malignant cells. ErbB3 and other members of the EGFR family have been implicated in cancer progression, it however remains unknown whether Ebp1 participate in prostate cancer progression <it>in vivo</it>. Therefore, the present study examines Ebp1 expression in cancerous and non-cancerous prostates tissues. Ebp1 expression was also correlated to known Ebp1 regulated proteins (Androgen receptor (AR), Cyclin D1 & ErbB3) and the proliferation marker Ki67. Furthermore we evaluated whether Ebp1 expression correlated with biochemical recurrence (BCR) following radical prostatectomy.</p> <p>Methods</p> <p>The expression of Ebp1, AR, Cyclin D1, ErbB3 and Ki67 were evaluated by immunohistochemistry using three separate tissue micro-arrays containing normal prostate tissues, non-cancerous tissue adjacent to the primary tumor, hormone-sensitive and hormone-refractory cancerous tissues. Multivariate COX regression analysis was performed with four clinical parameters in order to correlate Ebp1 expression with PCa progression.</p> <p>Results</p> <p>The expression of Ebp1 significantly increased with the progression from normal to hormone sensitive and to hormone refractory PCa. Furthermore, we observed strong correlation between Ebp1 expression and the nuclear expression of AR, Cyclin D1 and ErbB3 in both normal adjacent and cancer tissues. The expression of AR, Cyclin D1 and ErbB3 in normal adjacent tissues correlated with PSA relapse, whereas Ebp1 on its own did not significantly predict PSA relapse. Finally, in a multivariate analysis with a base clinical model (Gleason, Pre-op PSA, surgical margins and P-stage) we identified the multi-marker combination of Ebp1+/Cyclin D1- as an independent predictor of PSA relapse with a hazard ratio of 4.79.</p> <p>Conclusion</p> <p>Although not related to disease recurrence, this is the first <it>in vivo </it>study to report that Ebp1 expression correlates with PCa progression.</p> http://www.cancerci.com/content/8/1/18
collection DOAJ
language English
format Article
sources DOAJ
author Mes-Masson Anne-Marie
Karakiewicz Pierre I
Le Page Cécile
Koumakpayi Ismaël
Gannon Philippe O
Saad Fred
spellingShingle Mes-Masson Anne-Marie
Karakiewicz Pierre I
Le Page Cécile
Koumakpayi Ismaël
Gannon Philippe O
Saad Fred
Ebp1 expression in benign and malignant prostate
Cancer Cell International
author_facet Mes-Masson Anne-Marie
Karakiewicz Pierre I
Le Page Cécile
Koumakpayi Ismaël
Gannon Philippe O
Saad Fred
author_sort Mes-Masson Anne-Marie
title Ebp1 expression in benign and malignant prostate
title_short Ebp1 expression in benign and malignant prostate
title_full Ebp1 expression in benign and malignant prostate
title_fullStr Ebp1 expression in benign and malignant prostate
title_full_unstemmed Ebp1 expression in benign and malignant prostate
title_sort ebp1 expression in benign and malignant prostate
publisher BMC
series Cancer Cell International
issn 1475-2867
publishDate 2008-11-01
description <p>Abstract</p> <p>Background</p> <p>ErbB3-binding protein 1 (Ebp1) is a member of the <it>PA2G4 </it>family of proliferation-regulated proteins that is expressed in multiple malignant and non-malignant cells. ErbB3 and other members of the EGFR family have been implicated in cancer progression, it however remains unknown whether Ebp1 participate in prostate cancer progression <it>in vivo</it>. Therefore, the present study examines Ebp1 expression in cancerous and non-cancerous prostates tissues. Ebp1 expression was also correlated to known Ebp1 regulated proteins (Androgen receptor (AR), Cyclin D1 & ErbB3) and the proliferation marker Ki67. Furthermore we evaluated whether Ebp1 expression correlated with biochemical recurrence (BCR) following radical prostatectomy.</p> <p>Methods</p> <p>The expression of Ebp1, AR, Cyclin D1, ErbB3 and Ki67 were evaluated by immunohistochemistry using three separate tissue micro-arrays containing normal prostate tissues, non-cancerous tissue adjacent to the primary tumor, hormone-sensitive and hormone-refractory cancerous tissues. Multivariate COX regression analysis was performed with four clinical parameters in order to correlate Ebp1 expression with PCa progression.</p> <p>Results</p> <p>The expression of Ebp1 significantly increased with the progression from normal to hormone sensitive and to hormone refractory PCa. Furthermore, we observed strong correlation between Ebp1 expression and the nuclear expression of AR, Cyclin D1 and ErbB3 in both normal adjacent and cancer tissues. The expression of AR, Cyclin D1 and ErbB3 in normal adjacent tissues correlated with PSA relapse, whereas Ebp1 on its own did not significantly predict PSA relapse. Finally, in a multivariate analysis with a base clinical model (Gleason, Pre-op PSA, surgical margins and P-stage) we identified the multi-marker combination of Ebp1+/Cyclin D1- as an independent predictor of PSA relapse with a hazard ratio of 4.79.</p> <p>Conclusion</p> <p>Although not related to disease recurrence, this is the first <it>in vivo </it>study to report that Ebp1 expression correlates with PCa progression.</p>
url http://www.cancerci.com/content/8/1/18
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