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Shh Overexpression Is Correlated with GRP78 and AR Expression in Primary Prostate Cancer: Clinicopathological Features and Outcomes in a Chinese Cohort

INTRODUCTION: Shh plays an important role in prostate cancer progression, but its correlation with GRP78 and AR is elusive. METHODS: The study included 539 patients in total, of which 443 had primary prostate carcinoma and 96 patients had benign prostatic hyperplasia (BPH). The clinicopathologic fea...

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Autores principales: Zhang, Xiangyu, Zhang, Yanmin, Lin, Fanzhong, Shi, Xin, Xiang, Longquan, Li, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060775/
https://www.ncbi.nlm.nih.gov/pubmed/32184660
http://dx.doi.org/10.2147/CMAR.S231218
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author Zhang, Xiangyu
Zhang, Yanmin
Lin, Fanzhong
Shi, Xin
Xiang, Longquan
Li, Liang
author_facet Zhang, Xiangyu
Zhang, Yanmin
Lin, Fanzhong
Shi, Xin
Xiang, Longquan
Li, Liang
author_sort Zhang, Xiangyu
collection PubMed
description INTRODUCTION: Shh plays an important role in prostate cancer progression, but its correlation with GRP78 and AR is elusive. METHODS: The study included 539 patients in total, of which 443 had primary prostate carcinoma and 96 patients had benign prostatic hyperplasia (BPH). The clinicopathologic features, histologic scores of protein expression, and correlations between protein and disease state were studied in this cohort. Kaplan–Meier and Pearson correlation analyses were used to compare measures between groups. We performed immunohistochemistry to evaluate the expression of the Shh protein in benign prostatic hyperplasia (n=96) and prostate cancer (Gleason scores ≤6 [n=399] or ≥7 [n=44]). We quantified the expression of Shh, AR, and GRP78 using the weighted histoscore method, studied the correlation between Shh expression and AR and GRP78, and evaluated the impact of Shh protein expression on patient survival. RESULTS: Shh expression was significantly higher in prostate cancer with Gleason scores ≥7 than in cancer with lower Gleason scores or benign hyperplasia and was much higher in AR-positive cancer than in AR-negative cancer. Shh is overexpressed in high-grade prostate cancer and is positively correlated with the expression of both GRP78 and AR. CONCLUSION: Therefore, Shh may be a useful prognostic marker and therapeutic target for prostate cancer.
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spelling pubmed-70607752020-03-17 Shh Overexpression Is Correlated with GRP78 and AR Expression in Primary Prostate Cancer: Clinicopathological Features and Outcomes in a Chinese Cohort Zhang, Xiangyu Zhang, Yanmin Lin, Fanzhong Shi, Xin Xiang, Longquan Li, Liang Cancer Manag Res Original Research INTRODUCTION: Shh plays an important role in prostate cancer progression, but its correlation with GRP78 and AR is elusive. METHODS: The study included 539 patients in total, of which 443 had primary prostate carcinoma and 96 patients had benign prostatic hyperplasia (BPH). The clinicopathologic features, histologic scores of protein expression, and correlations between protein and disease state were studied in this cohort. Kaplan–Meier and Pearson correlation analyses were used to compare measures between groups. We performed immunohistochemistry to evaluate the expression of the Shh protein in benign prostatic hyperplasia (n=96) and prostate cancer (Gleason scores ≤6 [n=399] or ≥7 [n=44]). We quantified the expression of Shh, AR, and GRP78 using the weighted histoscore method, studied the correlation between Shh expression and AR and GRP78, and evaluated the impact of Shh protein expression on patient survival. RESULTS: Shh expression was significantly higher in prostate cancer with Gleason scores ≥7 than in cancer with lower Gleason scores or benign hyperplasia and was much higher in AR-positive cancer than in AR-negative cancer. Shh is overexpressed in high-grade prostate cancer and is positively correlated with the expression of both GRP78 and AR. CONCLUSION: Therefore, Shh may be a useful prognostic marker and therapeutic target for prostate cancer. Dove 2020-03-03 /pmc/articles/PMC7060775/ /pubmed/32184660 http://dx.doi.org/10.2147/CMAR.S231218 Text en © 2020 Zhang 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
Zhang, Xiangyu
Zhang, Yanmin
Lin, Fanzhong
Shi, Xin
Xiang, Longquan
Li, Liang
Shh Overexpression Is Correlated with GRP78 and AR Expression in Primary Prostate Cancer: Clinicopathological Features and Outcomes in a Chinese Cohort
title Shh Overexpression Is Correlated with GRP78 and AR Expression in Primary Prostate Cancer: Clinicopathological Features and Outcomes in a Chinese Cohort
title_full Shh Overexpression Is Correlated with GRP78 and AR Expression in Primary Prostate Cancer: Clinicopathological Features and Outcomes in a Chinese Cohort
title_fullStr Shh Overexpression Is Correlated with GRP78 and AR Expression in Primary Prostate Cancer: Clinicopathological Features and Outcomes in a Chinese Cohort
title_full_unstemmed Shh Overexpression Is Correlated with GRP78 and AR Expression in Primary Prostate Cancer: Clinicopathological Features and Outcomes in a Chinese Cohort
title_short Shh Overexpression Is Correlated with GRP78 and AR Expression in Primary Prostate Cancer: Clinicopathological Features and Outcomes in a Chinese Cohort
title_sort shh overexpression is correlated with grp78 and ar expression in primary prostate cancer: clinicopathological features and outcomes in a chinese cohort
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060775/
https://www.ncbi.nlm.nih.gov/pubmed/32184660
http://dx.doi.org/10.2147/CMAR.S231218
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