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ERG Protein Expression Is of Limited Prognostic Value in Men with Localized Prostate Cancer

Background. The prognostic significance of ERG expression in prostate cancer (PCA) has generated mixed results. We sought to investigate the prognostic significance of ERG expression in a localized cohort of men with PCA. Material and Methods. We investigated ERG protein expression in a cohort of 19...

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Autores principales: Teng, Liang Hong, Wang, Cheng, Dolph, Michael, Donnelly, Bryan, Bismar, Tarek A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762160/
https://www.ncbi.nlm.nih.gov/pubmed/24027643
http://dx.doi.org/10.1155/2013/786545
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author Teng, Liang Hong
Wang, Cheng
Dolph, Michael
Donnelly, Bryan
Bismar, Tarek A.
author_facet Teng, Liang Hong
Wang, Cheng
Dolph, Michael
Donnelly, Bryan
Bismar, Tarek A.
author_sort Teng, Liang Hong
collection PubMed
description Background. The prognostic significance of ERG expression in prostate cancer (PCA) has generated mixed results. We sought to investigate the prognostic significance of ERG expression in a localized cohort of men with PCA. Material and Methods. We investigated ERG protein expression in a cohort of 198 men with localized PCA. ERG expression was correlated with patients' clinical outcome and several pathological parameters, including Gleason score (GS), pathological stage, surgical margin, and extra-capsular extension. Results. ERG expression was detected in 86/198 (43.4%) patients exclusively in neoplastic epithelium. Overall, ERG mean expression intensity was 1.01 ± 1.27 versus 0.37 ± 0.83 in acinar PCA compared to foamy type PCA (P < 0.001). In HGPIN, ERG intensity levels were comparable to those in foamy type PCA (0.13 ± 0.56) but significantly lower than those in acinar PCA (P < 0.001). ERG expression was significantly associated with extra-prostatic extension and higher pathological stage and showed a trend toward seminal vesicle invasion. Herein, ERG expression was documented in 50/131 (38.1%) patients with pT2 versus 30/55 (54.5%) patients with pT3 (P = 0.04). ERG association with higher pathological stage was more pronounced in patients with GS > 7. Grouping patients into those with GS ≤ 7 versus >7, there was no significant association between ERG expression and GS. Similarly, no association was present in relation to either surgical margins or postsurgical serum PSA levels. Conclusion. We report significant association between ERG protein levels and extra-prostatic extension and higher pathological stage. ERG expression is not associated with adverse clinical outcome and is of limited prognostic value in localized PCA.
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spelling pubmed-37621602013-09-11 ERG Protein Expression Is of Limited Prognostic Value in Men with Localized Prostate Cancer Teng, Liang Hong Wang, Cheng Dolph, Michael Donnelly, Bryan Bismar, Tarek A. ISRN Urol Research Article Background. The prognostic significance of ERG expression in prostate cancer (PCA) has generated mixed results. We sought to investigate the prognostic significance of ERG expression in a localized cohort of men with PCA. Material and Methods. We investigated ERG protein expression in a cohort of 198 men with localized PCA. ERG expression was correlated with patients' clinical outcome and several pathological parameters, including Gleason score (GS), pathological stage, surgical margin, and extra-capsular extension. Results. ERG expression was detected in 86/198 (43.4%) patients exclusively in neoplastic epithelium. Overall, ERG mean expression intensity was 1.01 ± 1.27 versus 0.37 ± 0.83 in acinar PCA compared to foamy type PCA (P < 0.001). In HGPIN, ERG intensity levels were comparable to those in foamy type PCA (0.13 ± 0.56) but significantly lower than those in acinar PCA (P < 0.001). ERG expression was significantly associated with extra-prostatic extension and higher pathological stage and showed a trend toward seminal vesicle invasion. Herein, ERG expression was documented in 50/131 (38.1%) patients with pT2 versus 30/55 (54.5%) patients with pT3 (P = 0.04). ERG association with higher pathological stage was more pronounced in patients with GS > 7. Grouping patients into those with GS ≤ 7 versus >7, there was no significant association between ERG expression and GS. Similarly, no association was present in relation to either surgical margins or postsurgical serum PSA levels. Conclusion. We report significant association between ERG protein levels and extra-prostatic extension and higher pathological stage. ERG expression is not associated with adverse clinical outcome and is of limited prognostic value in localized PCA. Hindawi Publishing Corporation 2013-08-19 /pmc/articles/PMC3762160/ /pubmed/24027643 http://dx.doi.org/10.1155/2013/786545 Text en Copyright © 2013 Liang Hong Teng et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Teng, Liang Hong
Wang, Cheng
Dolph, Michael
Donnelly, Bryan
Bismar, Tarek A.
ERG Protein Expression Is of Limited Prognostic Value in Men with Localized Prostate Cancer
title ERG Protein Expression Is of Limited Prognostic Value in Men with Localized Prostate Cancer
title_full ERG Protein Expression Is of Limited Prognostic Value in Men with Localized Prostate Cancer
title_fullStr ERG Protein Expression Is of Limited Prognostic Value in Men with Localized Prostate Cancer
title_full_unstemmed ERG Protein Expression Is of Limited Prognostic Value in Men with Localized Prostate Cancer
title_short ERG Protein Expression Is of Limited Prognostic Value in Men with Localized Prostate Cancer
title_sort erg protein expression is of limited prognostic value in men with localized prostate cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762160/
https://www.ncbi.nlm.nih.gov/pubmed/24027643
http://dx.doi.org/10.1155/2013/786545
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