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Ribosome Binding Protein 1 Correlates with Prognosis and Cell Proliferation in Bladder Cancer

INTRODUCTION: Ribosome binding protein 1 (RRBP1) is reported to be correlated with tumor formation and progression. However, the role of RRBP1 in bladder cancer is unclear. In this study, we aimed to investigate the expression of RRBP1 and its influence on cell proliferation in bladder cancer. METHO...

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Autores principales: Lv, Shuang-wu, Shi, Zhen-guo, Wang, Xiao-hui, Zheng, Peng-yi, Li, Hui-bing, Han, Qing-jiang, Li, Zhi-jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367924/
https://www.ncbi.nlm.nih.gov/pubmed/32764960
http://dx.doi.org/10.2147/OTT.S252043
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author Lv, Shuang-wu
Shi, Zhen-guo
Wang, Xiao-hui
Zheng, Peng-yi
Li, Hui-bing
Han, Qing-jiang
Li, Zhi-jun
author_facet Lv, Shuang-wu
Shi, Zhen-guo
Wang, Xiao-hui
Zheng, Peng-yi
Li, Hui-bing
Han, Qing-jiang
Li, Zhi-jun
author_sort Lv, Shuang-wu
collection PubMed
description INTRODUCTION: Ribosome binding protein 1 (RRBP1) is reported to be correlated with tumor formation and progression. However, the role of RRBP1 in bladder cancer is unclear. In this study, we aimed to investigate the expression of RRBP1 and its influence on cell proliferation in bladder cancer. METHODS: Quantification real-time polymerase chain reaction (qRT-PCR) and immunohistochemistry (IHC) were used to detect the expression levels of RRBP1 in 138 bladder cancer and matched adjacent normal bladder tissues. Then, the clinical significance of RRBP1 in bladder cancer was evaluated. The effect of RRBP1 on cell proliferation and its potential mechanism were further explored. RESULTS: Results show that the mRNA levels of RRBP1 in bladder cancer were significantly higher compared with those in normal tissues (P< 0.001). IHC results show the high-expression rate of RRBP1 in bladder cancer was 68.8%, which was significantly greater than those in normal tissues (40.6%, P< 0.001). RRBP1 high-expression was significantly associated with differentiation, T stage and lymph node metastasis in bladder cancer (P< 0.05). The overall survival time of patients with RRBP1 high-expression was significantly reduced compared to those with RRBP1 low-expression. Moreover, RRBP1 overexpression significantly promoted cell proliferation, which was correlated with Smad1/Smad3/TGF-β1 signal pathway. CONCLUSION: RRBP1 high-expression correlates with prognosis and promotes cell proliferation in bladder cancer, which could be a potential biomarker.
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spelling pubmed-73679242020-08-05 Ribosome Binding Protein 1 Correlates with Prognosis and Cell Proliferation in Bladder Cancer Lv, Shuang-wu Shi, Zhen-guo Wang, Xiao-hui Zheng, Peng-yi Li, Hui-bing Han, Qing-jiang Li, Zhi-jun Onco Targets Ther Original Research INTRODUCTION: Ribosome binding protein 1 (RRBP1) is reported to be correlated with tumor formation and progression. However, the role of RRBP1 in bladder cancer is unclear. In this study, we aimed to investigate the expression of RRBP1 and its influence on cell proliferation in bladder cancer. METHODS: Quantification real-time polymerase chain reaction (qRT-PCR) and immunohistochemistry (IHC) were used to detect the expression levels of RRBP1 in 138 bladder cancer and matched adjacent normal bladder tissues. Then, the clinical significance of RRBP1 in bladder cancer was evaluated. The effect of RRBP1 on cell proliferation and its potential mechanism were further explored. RESULTS: Results show that the mRNA levels of RRBP1 in bladder cancer were significantly higher compared with those in normal tissues (P< 0.001). IHC results show the high-expression rate of RRBP1 in bladder cancer was 68.8%, which was significantly greater than those in normal tissues (40.6%, P< 0.001). RRBP1 high-expression was significantly associated with differentiation, T stage and lymph node metastasis in bladder cancer (P< 0.05). The overall survival time of patients with RRBP1 high-expression was significantly reduced compared to those with RRBP1 low-expression. Moreover, RRBP1 overexpression significantly promoted cell proliferation, which was correlated with Smad1/Smad3/TGF-β1 signal pathway. CONCLUSION: RRBP1 high-expression correlates with prognosis and promotes cell proliferation in bladder cancer, which could be a potential biomarker. Dove 2020-07-07 /pmc/articles/PMC7367924/ /pubmed/32764960 http://dx.doi.org/10.2147/OTT.S252043 Text en © 2020 Lv 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
Lv, Shuang-wu
Shi, Zhen-guo
Wang, Xiao-hui
Zheng, Peng-yi
Li, Hui-bing
Han, Qing-jiang
Li, Zhi-jun
Ribosome Binding Protein 1 Correlates with Prognosis and Cell Proliferation in Bladder Cancer
title Ribosome Binding Protein 1 Correlates with Prognosis and Cell Proliferation in Bladder Cancer
title_full Ribosome Binding Protein 1 Correlates with Prognosis and Cell Proliferation in Bladder Cancer
title_fullStr Ribosome Binding Protein 1 Correlates with Prognosis and Cell Proliferation in Bladder Cancer
title_full_unstemmed Ribosome Binding Protein 1 Correlates with Prognosis and Cell Proliferation in Bladder Cancer
title_short Ribosome Binding Protein 1 Correlates with Prognosis and Cell Proliferation in Bladder Cancer
title_sort ribosome binding protein 1 correlates with prognosis and cell proliferation in bladder cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367924/
https://www.ncbi.nlm.nih.gov/pubmed/32764960
http://dx.doi.org/10.2147/OTT.S252043
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