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ERG expression in prostate cancer biopsies with and without high-grade prostatic intraepithelial neoplasia: a study in Jordanian Arab patients

Background: High-grade prostatic intraepithelial neoplasia (HGPIN) is the most likely precancerous lesion for prostatic adenocarcinoma (PCa). Recent molecular studies have shown that HGPIN can harbor TMPRSS2-ERG fusion, a genetic marker also associated with PCa, which may provide an additional risk...

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Autores principales: Aldaoud, Najla, Graboski-Bauer, Ashley, Abdo, Nour, Al Bashir, Samir, Oweis, Ashraf O, Ebwaini, Hanadi, Hasen, Yousef, Alazab, Rami, Trpkov, Kiril
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535407/
https://www.ncbi.nlm.nih.gov/pubmed/31192172
http://dx.doi.org/10.2147/RRU.S207843
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author Aldaoud, Najla
Graboski-Bauer, Ashley
Abdo, Nour
Al Bashir, Samir
Oweis, Ashraf O
Ebwaini, Hanadi
Hasen, Yousef
Alazab, Rami
Trpkov, Kiril
author_facet Aldaoud, Najla
Graboski-Bauer, Ashley
Abdo, Nour
Al Bashir, Samir
Oweis, Ashraf O
Ebwaini, Hanadi
Hasen, Yousef
Alazab, Rami
Trpkov, Kiril
author_sort Aldaoud, Najla
collection PubMed
description Background: High-grade prostatic intraepithelial neoplasia (HGPIN) is the most likely precancerous lesion for prostatic adenocarcinoma (PCa). Recent molecular studies have shown that HGPIN can harbor TMPRSS2-ERG fusion, a genetic marker also associated with PCa, which may provide an additional risk stratification tool for HGPIN, especially when present as an isolated lesion. Our aim was to assess the frequency of HGPIN and ERG expression in a cohort of prostatic needle core biopsies from Jordanian-Arab patients with PCa. Materials and methods: We studied 109 needle core biopsies from patients with PCa. Clinical data, including age and preoperative prostate specific antigen (PSA) level, were obtained from patients’ medical records. Results: HGPIN was present in 31 (28.4 %) of the 109 cases. Of the HGPIN cases, 13 (41.9%) expressed ERG immunostain. ERG expression in HGPIN was independent of patient age at presentation (P=0.4), pre-operative PSA (P=0.9), and the grade, using the novel Grade Groups (P=0.5). Conclusion: The frequency of HGPIN in our cohort appears similar to the one found in the Western patient populations and demonstrates a comparable frequency of ERG expression in these lesions.
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spelling pubmed-65354072019-06-12 ERG expression in prostate cancer biopsies with and without high-grade prostatic intraepithelial neoplasia: a study in Jordanian Arab patients Aldaoud, Najla Graboski-Bauer, Ashley Abdo, Nour Al Bashir, Samir Oweis, Ashraf O Ebwaini, Hanadi Hasen, Yousef Alazab, Rami Trpkov, Kiril Res Rep Urol Original Research Background: High-grade prostatic intraepithelial neoplasia (HGPIN) is the most likely precancerous lesion for prostatic adenocarcinoma (PCa). Recent molecular studies have shown that HGPIN can harbor TMPRSS2-ERG fusion, a genetic marker also associated with PCa, which may provide an additional risk stratification tool for HGPIN, especially when present as an isolated lesion. Our aim was to assess the frequency of HGPIN and ERG expression in a cohort of prostatic needle core biopsies from Jordanian-Arab patients with PCa. Materials and methods: We studied 109 needle core biopsies from patients with PCa. Clinical data, including age and preoperative prostate specific antigen (PSA) level, were obtained from patients’ medical records. Results: HGPIN was present in 31 (28.4 %) of the 109 cases. Of the HGPIN cases, 13 (41.9%) expressed ERG immunostain. ERG expression in HGPIN was independent of patient age at presentation (P=0.4), pre-operative PSA (P=0.9), and the grade, using the novel Grade Groups (P=0.5). Conclusion: The frequency of HGPIN in our cohort appears similar to the one found in the Western patient populations and demonstrates a comparable frequency of ERG expression in these lesions. Dove 2019-05-22 /pmc/articles/PMC6535407/ /pubmed/31192172 http://dx.doi.org/10.2147/RRU.S207843 Text en © 2019 Aldaoud et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Aldaoud, Najla
Graboski-Bauer, Ashley
Abdo, Nour
Al Bashir, Samir
Oweis, Ashraf O
Ebwaini, Hanadi
Hasen, Yousef
Alazab, Rami
Trpkov, Kiril
ERG expression in prostate cancer biopsies with and without high-grade prostatic intraepithelial neoplasia: a study in Jordanian Arab patients
title ERG expression in prostate cancer biopsies with and without high-grade prostatic intraepithelial neoplasia: a study in Jordanian Arab patients
title_full ERG expression in prostate cancer biopsies with and without high-grade prostatic intraepithelial neoplasia: a study in Jordanian Arab patients
title_fullStr ERG expression in prostate cancer biopsies with and without high-grade prostatic intraepithelial neoplasia: a study in Jordanian Arab patients
title_full_unstemmed ERG expression in prostate cancer biopsies with and without high-grade prostatic intraepithelial neoplasia: a study in Jordanian Arab patients
title_short ERG expression in prostate cancer biopsies with and without high-grade prostatic intraepithelial neoplasia: a study in Jordanian Arab patients
title_sort erg expression in prostate cancer biopsies with and without high-grade prostatic intraepithelial neoplasia: a study in jordanian arab patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535407/
https://www.ncbi.nlm.nih.gov/pubmed/31192172
http://dx.doi.org/10.2147/RRU.S207843
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