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Increased expression of miR-222 is associated with poor prognosis in bladder cancer

BACKGROUND: MicroRNA-222 (miR-222) has been shown to play a potential oncogenic role in bladder cancer. The aim of this study was to evaluate the expression of miR-222 in bladder cancer and its potential relevance to clinicopathological characteristics and patient survival. METHODS: Surgical specime...

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Autores principales: Zhang, Dong-qing, Zhou, Chang-kuo, Jiang, Xue-wen, Chen, Jun, Shi, Ben-kang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132207/
https://www.ncbi.nlm.nih.gov/pubmed/25078265
http://dx.doi.org/10.1186/1477-7819-12-241
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author Zhang, Dong-qing
Zhou, Chang-kuo
Jiang, Xue-wen
Chen, Jun
Shi, Ben-kang
author_facet Zhang, Dong-qing
Zhou, Chang-kuo
Jiang, Xue-wen
Chen, Jun
Shi, Ben-kang
author_sort Zhang, Dong-qing
collection PubMed
description BACKGROUND: MicroRNA-222 (miR-222) has been shown to play a potential oncogenic role in bladder cancer. The aim of this study was to evaluate the expression of miR-222 in bladder cancer and its potential relevance to clinicopathological characteristics and patient survival. METHODS: Surgical specimens of cancer tissue and adjacent normal tissue were obtained from 97 patients with bladder cancer. The relative expression levels of miR-222 in the cancer and the normal adjacent tissue were measured by quantitative reverse-transcriptase PCR. We analyzed their correlation with clinicopathological parameters and prognostic value. RESULTS: The expression level of miR-222 was significantly higher in tumor tissues than in corresponding non-cancerous tissues (5.46 ± 1.45 versus 1.92 ± 0.65, P < 0.0001), and a high expression of miR-222 was found to be significantly associated with tumor grade (P = 0.003) and tumor stage (P = 0.005). The miR-222 expression level was classified as high or low in relation to the median value (cutoff value = 5.15). Kaplan-Meier analysis showed that patients with higher levels of miR-222 had significantly poorer survival than those with lower expression of this miRNA in patients, with a 5-year overall survival of 29.53% and 52.75%, respectively (P = 0.0034). In the multivariate Cox proportional hazards analysis, which included miR-222 level, tumor grade, tumor stage, and tumor number, high miR-222 expression was independently associated with poor survival (P < 0.001; hazard ratio 6.17; 95% CI 2.33 to 10.39). CONCLUSION: miR-222 overexpression is involved in the poor prognosis of bladder cancer and can be used as a biomarker for selection of cases requiring special attention.
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spelling pubmed-41322072014-08-15 Increased expression of miR-222 is associated with poor prognosis in bladder cancer Zhang, Dong-qing Zhou, Chang-kuo Jiang, Xue-wen Chen, Jun Shi, Ben-kang World J Surg Oncol Research BACKGROUND: MicroRNA-222 (miR-222) has been shown to play a potential oncogenic role in bladder cancer. The aim of this study was to evaluate the expression of miR-222 in bladder cancer and its potential relevance to clinicopathological characteristics and patient survival. METHODS: Surgical specimens of cancer tissue and adjacent normal tissue were obtained from 97 patients with bladder cancer. The relative expression levels of miR-222 in the cancer and the normal adjacent tissue were measured by quantitative reverse-transcriptase PCR. We analyzed their correlation with clinicopathological parameters and prognostic value. RESULTS: The expression level of miR-222 was significantly higher in tumor tissues than in corresponding non-cancerous tissues (5.46 ± 1.45 versus 1.92 ± 0.65, P < 0.0001), and a high expression of miR-222 was found to be significantly associated with tumor grade (P = 0.003) and tumor stage (P = 0.005). The miR-222 expression level was classified as high or low in relation to the median value (cutoff value = 5.15). Kaplan-Meier analysis showed that patients with higher levels of miR-222 had significantly poorer survival than those with lower expression of this miRNA in patients, with a 5-year overall survival of 29.53% and 52.75%, respectively (P = 0.0034). In the multivariate Cox proportional hazards analysis, which included miR-222 level, tumor grade, tumor stage, and tumor number, high miR-222 expression was independently associated with poor survival (P < 0.001; hazard ratio 6.17; 95% CI 2.33 to 10.39). CONCLUSION: miR-222 overexpression is involved in the poor prognosis of bladder cancer and can be used as a biomarker for selection of cases requiring special attention. BioMed Central 2014-07-31 /pmc/articles/PMC4132207/ /pubmed/25078265 http://dx.doi.org/10.1186/1477-7819-12-241 Text en Copyright © 2014 Zhang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Zhang, Dong-qing
Zhou, Chang-kuo
Jiang, Xue-wen
Chen, Jun
Shi, Ben-kang
Increased expression of miR-222 is associated with poor prognosis in bladder cancer
title Increased expression of miR-222 is associated with poor prognosis in bladder cancer
title_full Increased expression of miR-222 is associated with poor prognosis in bladder cancer
title_fullStr Increased expression of miR-222 is associated with poor prognosis in bladder cancer
title_full_unstemmed Increased expression of miR-222 is associated with poor prognosis in bladder cancer
title_short Increased expression of miR-222 is associated with poor prognosis in bladder cancer
title_sort increased expression of mir-222 is associated with poor prognosis in bladder cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132207/
https://www.ncbi.nlm.nih.gov/pubmed/25078265
http://dx.doi.org/10.1186/1477-7819-12-241
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