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Higher expression of FOXOs correlates to better prognosis of bladder cancer

BACKGROUND: We aimed to explore the expression of forkhead box class O (FOXO) and relations between expressions of FOXOs and clinicopathological characteristics and prognosis of bladder cancer. METHODS: We enrolled a cohort of 276 patients with bladder cancer in our study. Expressions of FOXOs in bl...

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Detalles Bibliográficos
Autores principales: Zhang, Ying, Jia, Linpei, Ji, Wei, Li, Hai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707102/
https://www.ncbi.nlm.nih.gov/pubmed/29221208
http://dx.doi.org/10.18632/oncotarget.22029
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author Zhang, Ying
Jia, Linpei
Zhang, Ying
Ji, Wei
Li, Hai
author_facet Zhang, Ying
Jia, Linpei
Zhang, Ying
Ji, Wei
Li, Hai
author_sort Zhang, Ying
collection PubMed
description BACKGROUND: We aimed to explore the expression of forkhead box class O (FOXO) and relations between expressions of FOXOs and clinicopathological characteristics and prognosis of bladder cancer. METHODS: We enrolled a cohort of 276 patients with bladder cancer in our study. Expressions of FOXOs in bladder cancer tissue and adjacent tissue were measured by quantitative real-time polymerase chain reaction (qRT-PCR) and immunohistochemistry (IHC). Correlations between expression of FOXOs and clinicopathological characteristics and prognosis were analyzed. The relationship between expression of FOXOs and survival time of patients with bladder cancer was analyzed by the Kaplan-Meier survival analysis and the Log-rank test; individual variables which may affect the prognosis of bladder cancer were detected by the Cox proportional hazard regression model. RESULTS: Compared with bladder cancer tissue, a higher expression of FOXOs was detected in paracancerous tissue. We found significant associations between histological grade and the expressions of FOXOs, clinical stage and the expressions of FOXOs, and lymph node metastasis and the expressions of FOXOs (all P < 0.05). When used for diagnosing bladder cancer, the mRNA expression of FOXO1/3/4 produced cut off values of 1.475, 1.305, and 1.295, respectively, exhibiting relatively high specificity and sensitivity. The Kaplan-Meier curves indicated that patients with a higher expression of FOXOs tended to have a longer overall survival than those with lower expression. The Cox regression analysis revealed that lymph node metastasis, high clinical stage, and low expression of FOXOs were independent risk factors for bladder cancer prognosis. CONCLUSION: Our results indicate that the expression of FOXOs is closely correlated with clinicopathological characteristics and prognosis of bladder cancer.
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spelling pubmed-57071022017-12-07 Higher expression of FOXOs correlates to better prognosis of bladder cancer Zhang, Ying Jia, Linpei Zhang, Ying Ji, Wei Li, Hai Oncotarget Research Paper BACKGROUND: We aimed to explore the expression of forkhead box class O (FOXO) and relations between expressions of FOXOs and clinicopathological characteristics and prognosis of bladder cancer. METHODS: We enrolled a cohort of 276 patients with bladder cancer in our study. Expressions of FOXOs in bladder cancer tissue and adjacent tissue were measured by quantitative real-time polymerase chain reaction (qRT-PCR) and immunohistochemistry (IHC). Correlations between expression of FOXOs and clinicopathological characteristics and prognosis were analyzed. The relationship between expression of FOXOs and survival time of patients with bladder cancer was analyzed by the Kaplan-Meier survival analysis and the Log-rank test; individual variables which may affect the prognosis of bladder cancer were detected by the Cox proportional hazard regression model. RESULTS: Compared with bladder cancer tissue, a higher expression of FOXOs was detected in paracancerous tissue. We found significant associations between histological grade and the expressions of FOXOs, clinical stage and the expressions of FOXOs, and lymph node metastasis and the expressions of FOXOs (all P < 0.05). When used for diagnosing bladder cancer, the mRNA expression of FOXO1/3/4 produced cut off values of 1.475, 1.305, and 1.295, respectively, exhibiting relatively high specificity and sensitivity. The Kaplan-Meier curves indicated that patients with a higher expression of FOXOs tended to have a longer overall survival than those with lower expression. The Cox regression analysis revealed that lymph node metastasis, high clinical stage, and low expression of FOXOs were independent risk factors for bladder cancer prognosis. CONCLUSION: Our results indicate that the expression of FOXOs is closely correlated with clinicopathological characteristics and prognosis of bladder cancer. Impact Journals LLC 2017-10-24 /pmc/articles/PMC5707102/ /pubmed/29221208 http://dx.doi.org/10.18632/oncotarget.22029 Text en Copyright: © 2017 Zhang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Zhang, Ying
Jia, Linpei
Zhang, Ying
Ji, Wei
Li, Hai
Higher expression of FOXOs correlates to better prognosis of bladder cancer
title Higher expression of FOXOs correlates to better prognosis of bladder cancer
title_full Higher expression of FOXOs correlates to better prognosis of bladder cancer
title_fullStr Higher expression of FOXOs correlates to better prognosis of bladder cancer
title_full_unstemmed Higher expression of FOXOs correlates to better prognosis of bladder cancer
title_short Higher expression of FOXOs correlates to better prognosis of bladder cancer
title_sort higher expression of foxos correlates to better prognosis of bladder cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707102/
https://www.ncbi.nlm.nih.gov/pubmed/29221208
http://dx.doi.org/10.18632/oncotarget.22029
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