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Clinicopathological impacts of c-Met overexpression in bladder cancer: evidence from 1,336 cases
Background: The clinicopathological impacts of c-Met overexpression in bladder cancer have been investigated in several studies with conflicting results. We performed this systematic review and meta-analysis to assess the pathologic and prognostic roles of c-Met status in bladder cancer patients. Me...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497828/ https://www.ncbi.nlm.nih.gov/pubmed/31114223 http://dx.doi.org/10.2147/OTT.S197540 |
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author | Xu, Xin Zhang, Guanjun He, Liujia Zhu, Yi |
author_facet | Xu, Xin Zhang, Guanjun He, Liujia Zhu, Yi |
author_sort | Xu, Xin |
collection | PubMed |
description | Background: The clinicopathological impacts of c-Met overexpression in bladder cancer have been investigated in several studies with conflicting results. We performed this systematic review and meta-analysis to assess the pathologic and prognostic roles of c-Met status in bladder cancer patients. Methods: Eligible studies were searched and identified from the PubMed and China National Knowledge Infrastructure (CNKI) databases (up until October 4, 2018). The DerSimonian-Laird random-effects model was used to calculate the pooled risk estimates. Results: Eight studies including 1,336 bladder cancer cases were eventually included in this meta-analysis. We detected a significantly increased risk of poor overall survival (OS) associated with the high expression of c-Met (HR=2.42, 95% CI 1.36–4.32). There was no association between c-Met status and nuclear grade (OR=0.82, 95% CI 0.29–2.31) or tumor stage (OR=1.42, 95% CI 0.41–4.89). Conclusion: This study shows that the overexpression of c-Met in primary cancer tissues is associated with a worse OS in human bladder cancer. However, larger studies using standardized methods and criteria are warranted to verify these findings. |
format | Online Article Text |
id | pubmed-6497828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-64978282019-05-21 Clinicopathological impacts of c-Met overexpression in bladder cancer: evidence from 1,336 cases Xu, Xin Zhang, Guanjun He, Liujia Zhu, Yi Onco Targets Ther Original Research Background: The clinicopathological impacts of c-Met overexpression in bladder cancer have been investigated in several studies with conflicting results. We performed this systematic review and meta-analysis to assess the pathologic and prognostic roles of c-Met status in bladder cancer patients. Methods: Eligible studies were searched and identified from the PubMed and China National Knowledge Infrastructure (CNKI) databases (up until October 4, 2018). The DerSimonian-Laird random-effects model was used to calculate the pooled risk estimates. Results: Eight studies including 1,336 bladder cancer cases were eventually included in this meta-analysis. We detected a significantly increased risk of poor overall survival (OS) associated with the high expression of c-Met (HR=2.42, 95% CI 1.36–4.32). There was no association between c-Met status and nuclear grade (OR=0.82, 95% CI 0.29–2.31) or tumor stage (OR=1.42, 95% CI 0.41–4.89). Conclusion: This study shows that the overexpression of c-Met in primary cancer tissues is associated with a worse OS in human bladder cancer. However, larger studies using standardized methods and criteria are warranted to verify these findings. Dove 2019-04-10 /pmc/articles/PMC6497828/ /pubmed/31114223 http://dx.doi.org/10.2147/OTT.S197540 Text en © 2019 Xu 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 Xu, Xin Zhang, Guanjun He, Liujia Zhu, Yi Clinicopathological impacts of c-Met overexpression in bladder cancer: evidence from 1,336 cases |
title | Clinicopathological impacts of c-Met overexpression in bladder cancer: evidence from 1,336 cases |
title_full | Clinicopathological impacts of c-Met overexpression in bladder cancer: evidence from 1,336 cases |
title_fullStr | Clinicopathological impacts of c-Met overexpression in bladder cancer: evidence from 1,336 cases |
title_full_unstemmed | Clinicopathological impacts of c-Met overexpression in bladder cancer: evidence from 1,336 cases |
title_short | Clinicopathological impacts of c-Met overexpression in bladder cancer: evidence from 1,336 cases |
title_sort | clinicopathological impacts of c-met overexpression in bladder cancer: evidence from 1,336 cases |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497828/ https://www.ncbi.nlm.nih.gov/pubmed/31114223 http://dx.doi.org/10.2147/OTT.S197540 |
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