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Androgen receptor mRNA expression is a predictor for recurrence-free survival in non-muscle invasive bladder cancer

BACKGROUND: Non-muscular invasive bladder cancer (NMIBC) has a high risk of recurrence. As androgen receptor (AR) reportedly affects bladder cancer, we assessed the correlation between NMIBC recurrence and tumor AR expression in Japanese patients. METHODS: We retrospectively reviewed 53 specimens of...

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Autores principales: Yasui, Masato, Kawahara, Takashi, Izumi, Koji, Yao, Masahiro, Ishiguro, Yukari, Ishiguro, Hitoshi, Uemura, Hiroji, Miyoshi, Yasuhide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454612/
https://www.ncbi.nlm.nih.gov/pubmed/30961575
http://dx.doi.org/10.1186/s12885-019-5512-9
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author Yasui, Masato
Kawahara, Takashi
Izumi, Koji
Yao, Masahiro
Ishiguro, Yukari
Ishiguro, Hitoshi
Uemura, Hiroji
Miyoshi, Yasuhide
author_facet Yasui, Masato
Kawahara, Takashi
Izumi, Koji
Yao, Masahiro
Ishiguro, Yukari
Ishiguro, Hitoshi
Uemura, Hiroji
Miyoshi, Yasuhide
author_sort Yasui, Masato
collection PubMed
description BACKGROUND: Non-muscular invasive bladder cancer (NMIBC) has a high risk of recurrence. As androgen receptor (AR) reportedly affects bladder cancer, we assessed the correlation between NMIBC recurrence and tumor AR expression in Japanese patients. METHODS: We retrospectively reviewed 53 specimens of non-metastatic NMIBC, with recurrence-free survival (RFS) as the primary endpoint. We used real-time quantitative polymerase chain reaction to quantify AR mRNA expression. Kaplan–Meier product-limit estimators were used to assess RFS distribution, log-rank tests to analyze differences in RFS between high- and low-risk groups; and multivariate analyses of AR mRNA expression and other clinicopathological factors to predict independent factors for RFS. RESULTS: The high AR mRNA-expressing group (n = 43) tended to have a longer median RFS (not reached) than did the low-AR group (n = 10; 9.04 months; P = 0.112). Multivariate analysis showed female sex (hazard ratio [HR]: 7.360, 95% CI: 1.649–32.856, P = 0.009), tumor size ≥3 cm (HR: 23.697, 95% CI: 4.383–128.117, P < 0.001) and low AR mRNA expression (HR: 0.202, 95% CI: 0.048–0.841, P = 0.028) to be independent predictors of shorter RFS. CONCLUSION: Our study showed that low AR mRNA expression level is an independent risk factor for RFS in Japanese patients with NMIBC. Further studies are necessary but AR expression might be a new indicator of recurrence of NMIBC.
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spelling pubmed-64546122019-04-19 Androgen receptor mRNA expression is a predictor for recurrence-free survival in non-muscle invasive bladder cancer Yasui, Masato Kawahara, Takashi Izumi, Koji Yao, Masahiro Ishiguro, Yukari Ishiguro, Hitoshi Uemura, Hiroji Miyoshi, Yasuhide BMC Cancer Research Article BACKGROUND: Non-muscular invasive bladder cancer (NMIBC) has a high risk of recurrence. As androgen receptor (AR) reportedly affects bladder cancer, we assessed the correlation between NMIBC recurrence and tumor AR expression in Japanese patients. METHODS: We retrospectively reviewed 53 specimens of non-metastatic NMIBC, with recurrence-free survival (RFS) as the primary endpoint. We used real-time quantitative polymerase chain reaction to quantify AR mRNA expression. Kaplan–Meier product-limit estimators were used to assess RFS distribution, log-rank tests to analyze differences in RFS between high- and low-risk groups; and multivariate analyses of AR mRNA expression and other clinicopathological factors to predict independent factors for RFS. RESULTS: The high AR mRNA-expressing group (n = 43) tended to have a longer median RFS (not reached) than did the low-AR group (n = 10; 9.04 months; P = 0.112). Multivariate analysis showed female sex (hazard ratio [HR]: 7.360, 95% CI: 1.649–32.856, P = 0.009), tumor size ≥3 cm (HR: 23.697, 95% CI: 4.383–128.117, P < 0.001) and low AR mRNA expression (HR: 0.202, 95% CI: 0.048–0.841, P = 0.028) to be independent predictors of shorter RFS. CONCLUSION: Our study showed that low AR mRNA expression level is an independent risk factor for RFS in Japanese patients with NMIBC. Further studies are necessary but AR expression might be a new indicator of recurrence of NMIBC. BioMed Central 2019-04-08 /pmc/articles/PMC6454612/ /pubmed/30961575 http://dx.doi.org/10.1186/s12885-019-5512-9 Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Yasui, Masato
Kawahara, Takashi
Izumi, Koji
Yao, Masahiro
Ishiguro, Yukari
Ishiguro, Hitoshi
Uemura, Hiroji
Miyoshi, Yasuhide
Androgen receptor mRNA expression is a predictor for recurrence-free survival in non-muscle invasive bladder cancer
title Androgen receptor mRNA expression is a predictor for recurrence-free survival in non-muscle invasive bladder cancer
title_full Androgen receptor mRNA expression is a predictor for recurrence-free survival in non-muscle invasive bladder cancer
title_fullStr Androgen receptor mRNA expression is a predictor for recurrence-free survival in non-muscle invasive bladder cancer
title_full_unstemmed Androgen receptor mRNA expression is a predictor for recurrence-free survival in non-muscle invasive bladder cancer
title_short Androgen receptor mRNA expression is a predictor for recurrence-free survival in non-muscle invasive bladder cancer
title_sort androgen receptor mrna expression is a predictor for recurrence-free survival in non-muscle invasive bladder cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454612/
https://www.ncbi.nlm.nih.gov/pubmed/30961575
http://dx.doi.org/10.1186/s12885-019-5512-9
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