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The clinicopathological and prognostic value of CD44 expression in bladder cancer: a study based on meta-analysis and TCGA data

CD44 is reported to be involved in tumor invasion and metastasis. However, the role of cancer stem cell marker CD44 in bladder cancer still remains controversial. Hence, the correlations between CD44 expression and the clinicopathological features and the prognosis of bladder cancer were investigate...

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Autores principales: Hu, Yu, Zhang, Yongrui, Gao, Jialin, Lian, Xin, Wang, Yuantao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250188/
https://www.ncbi.nlm.nih.gov/pubmed/32434417
http://dx.doi.org/10.1080/21655979.2020.1765500
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author Hu, Yu
Zhang, Yongrui
Gao, Jialin
Lian, Xin
Wang, Yuantao
author_facet Hu, Yu
Zhang, Yongrui
Gao, Jialin
Lian, Xin
Wang, Yuantao
author_sort Hu, Yu
collection PubMed
description CD44 is reported to be involved in tumor invasion and metastasis. However, the role of cancer stem cell marker CD44 in bladder cancer still remains controversial. Hence, the correlations between CD44 expression and the clinicopathological features and the prognosis of bladder cancer were investigated. Publications using immunohistochemical methods were identified. The Cancer Genome Atlas (TCGA) data were also analyzed. The odds ratios (ORs) or hazard ratios (HRs) with their 95% confidence intervals (95% CIs) were calculated. 14 studies involving 1107 tissue samples were included. CD44 expression in bladder cancer was lower than in non-tumor tissue samples (OR = 0.14, P = 0.005), which was consistent with TCGA data. CD44 expression was correlated with advanced T stage (OR = 1.76, P = 0.029) and lymph node metastasis (OR = 4.09, P < 0.001). Multivariate survival analysis showed that CD44 expression was not linked to tumor-specific survival, overall survival, and recurrence/relapse-free survival, but was associated with disease failure (HR = 2.912, 95% CI = 1.51–5.61). No relationships of CD44 expression with the clinicopathological features and overall survival were found from TCGA data. Our finding suggested that CD44 expression may be correlated with progression, metastasis, and disease failure of bladder cancer. However, further large-scale studies are needed. Abbreviations: CD44: Cluster of Differentiation 44; CIs: Confidence Intervals; CSCs: Cancer Stem Cells; EMT: Epithelial-mesenchymal Transition; HRs: Hazard Ratios; ORs: Odds Ratios; TCGA: The Cancer Genome Atlas
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spelling pubmed-72501882021-05-20 The clinicopathological and prognostic value of CD44 expression in bladder cancer: a study based on meta-analysis and TCGA data Hu, Yu Zhang, Yongrui Gao, Jialin Lian, Xin Wang, Yuantao Bioengineered Research Paper CD44 is reported to be involved in tumor invasion and metastasis. However, the role of cancer stem cell marker CD44 in bladder cancer still remains controversial. Hence, the correlations between CD44 expression and the clinicopathological features and the prognosis of bladder cancer were investigated. Publications using immunohistochemical methods were identified. The Cancer Genome Atlas (TCGA) data were also analyzed. The odds ratios (ORs) or hazard ratios (HRs) with their 95% confidence intervals (95% CIs) were calculated. 14 studies involving 1107 tissue samples were included. CD44 expression in bladder cancer was lower than in non-tumor tissue samples (OR = 0.14, P = 0.005), which was consistent with TCGA data. CD44 expression was correlated with advanced T stage (OR = 1.76, P = 0.029) and lymph node metastasis (OR = 4.09, P < 0.001). Multivariate survival analysis showed that CD44 expression was not linked to tumor-specific survival, overall survival, and recurrence/relapse-free survival, but was associated with disease failure (HR = 2.912, 95% CI = 1.51–5.61). No relationships of CD44 expression with the clinicopathological features and overall survival were found from TCGA data. Our finding suggested that CD44 expression may be correlated with progression, metastasis, and disease failure of bladder cancer. However, further large-scale studies are needed. Abbreviations: CD44: Cluster of Differentiation 44; CIs: Confidence Intervals; CSCs: Cancer Stem Cells; EMT: Epithelial-mesenchymal Transition; HRs: Hazard Ratios; ORs: Odds Ratios; TCGA: The Cancer Genome Atlas Taylor & Francis 2020-05-20 /pmc/articles/PMC7250188/ /pubmed/32434417 http://dx.doi.org/10.1080/21655979.2020.1765500 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://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/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Hu, Yu
Zhang, Yongrui
Gao, Jialin
Lian, Xin
Wang, Yuantao
The clinicopathological and prognostic value of CD44 expression in bladder cancer: a study based on meta-analysis and TCGA data
title The clinicopathological and prognostic value of CD44 expression in bladder cancer: a study based on meta-analysis and TCGA data
title_full The clinicopathological and prognostic value of CD44 expression in bladder cancer: a study based on meta-analysis and TCGA data
title_fullStr The clinicopathological and prognostic value of CD44 expression in bladder cancer: a study based on meta-analysis and TCGA data
title_full_unstemmed The clinicopathological and prognostic value of CD44 expression in bladder cancer: a study based on meta-analysis and TCGA data
title_short The clinicopathological and prognostic value of CD44 expression in bladder cancer: a study based on meta-analysis and TCGA data
title_sort clinicopathological and prognostic value of cd44 expression in bladder cancer: a study based on meta-analysis and tcga data
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250188/
https://www.ncbi.nlm.nih.gov/pubmed/32434417
http://dx.doi.org/10.1080/21655979.2020.1765500
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