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Prognostic Significance of MET Amplification and Expression in Gastric Cancer: A Systematic Review with Meta-Analysis

BACKGROUND AND AIMS: MET, the hepatocyte growth factor receptor, is a receptor tyrosine kinase overexpressed and activated in a subset of gastric cancer. Several studies investigated the relationship between MET amplification and expression with the clinical outcome in patients with gastric cancer,...

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Autores principales: Peng, Zhi, Zhu, Yan, Wang, Qianqian, Gao, Jing, Li, Yilin, Li, Yanyan, Ge, Sai, Shen, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885582/
https://www.ncbi.nlm.nih.gov/pubmed/24416238
http://dx.doi.org/10.1371/journal.pone.0084502
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author Peng, Zhi
Zhu, Yan
Wang, Qianqian
Gao, Jing
Li, Yilin
Li, Yanyan
Ge, Sai
Shen, Lin
author_facet Peng, Zhi
Zhu, Yan
Wang, Qianqian
Gao, Jing
Li, Yilin
Li, Yanyan
Ge, Sai
Shen, Lin
author_sort Peng, Zhi
collection PubMed
description BACKGROUND AND AIMS: MET, the hepatocyte growth factor receptor, is a receptor tyrosine kinase overexpressed and activated in a subset of gastric cancer. Several studies investigated the relationship between MET amplification and expression with the clinical outcome in patients with gastric cancer, but yielded conflicting results. We performed a systematic review and meta-analysis to determine the influence of MET amplification and expression on prognosis in gastric cancer. METHODS: MEDLINE and EMBASE were searched for studies that explored the association between MET amplification and expression with survival in patients with gastric cancer up to 1 April, 2013. Data of individual hazard ratios (HRs) and 95% confidence intervals (CIs) for meta-analyses were extracted from the publications and combined in pooled HRs. RESULTS: Fourteen studies involving 2,258 patients with gastric cancer were included. It was suggested that MET overexpression had an unfavorable impact on survival of patients with gastric cancer, with HRs (95% CIs) of 2.57 (95% CI: 1.97–3.35) overall, 2.82 (95% CI: 1.86–4.27) among studies using amplification for measure scale of MET and 2.42 (95% CI: 1.66–3.54) for expression. The magnitude of association was reduced whereas remained statistically significant in high quality studies or in larger sample size studies and corresponding HRs were 2.18(1.76, 2.70) and 2.35(1.93, 2.87), respectively, without significant heterogeneity. CONCLUSION: The findings from present study indicated that higher MET gene amplification and expression in gastric cancer was an indicator of poor prognosis.
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spelling pubmed-38855822014-01-10 Prognostic Significance of MET Amplification and Expression in Gastric Cancer: A Systematic Review with Meta-Analysis Peng, Zhi Zhu, Yan Wang, Qianqian Gao, Jing Li, Yilin Li, Yanyan Ge, Sai Shen, Lin PLoS One Research Article BACKGROUND AND AIMS: MET, the hepatocyte growth factor receptor, is a receptor tyrosine kinase overexpressed and activated in a subset of gastric cancer. Several studies investigated the relationship between MET amplification and expression with the clinical outcome in patients with gastric cancer, but yielded conflicting results. We performed a systematic review and meta-analysis to determine the influence of MET amplification and expression on prognosis in gastric cancer. METHODS: MEDLINE and EMBASE were searched for studies that explored the association between MET amplification and expression with survival in patients with gastric cancer up to 1 April, 2013. Data of individual hazard ratios (HRs) and 95% confidence intervals (CIs) for meta-analyses were extracted from the publications and combined in pooled HRs. RESULTS: Fourteen studies involving 2,258 patients with gastric cancer were included. It was suggested that MET overexpression had an unfavorable impact on survival of patients with gastric cancer, with HRs (95% CIs) of 2.57 (95% CI: 1.97–3.35) overall, 2.82 (95% CI: 1.86–4.27) among studies using amplification for measure scale of MET and 2.42 (95% CI: 1.66–3.54) for expression. The magnitude of association was reduced whereas remained statistically significant in high quality studies or in larger sample size studies and corresponding HRs were 2.18(1.76, 2.70) and 2.35(1.93, 2.87), respectively, without significant heterogeneity. CONCLUSION: The findings from present study indicated that higher MET gene amplification and expression in gastric cancer was an indicator of poor prognosis. Public Library of Science 2014-01-08 /pmc/articles/PMC3885582/ /pubmed/24416238 http://dx.doi.org/10.1371/journal.pone.0084502 Text en © 2014 Peng et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Peng, Zhi
Zhu, Yan
Wang, Qianqian
Gao, Jing
Li, Yilin
Li, Yanyan
Ge, Sai
Shen, Lin
Prognostic Significance of MET Amplification and Expression in Gastric Cancer: A Systematic Review with Meta-Analysis
title Prognostic Significance of MET Amplification and Expression in Gastric Cancer: A Systematic Review with Meta-Analysis
title_full Prognostic Significance of MET Amplification and Expression in Gastric Cancer: A Systematic Review with Meta-Analysis
title_fullStr Prognostic Significance of MET Amplification and Expression in Gastric Cancer: A Systematic Review with Meta-Analysis
title_full_unstemmed Prognostic Significance of MET Amplification and Expression in Gastric Cancer: A Systematic Review with Meta-Analysis
title_short Prognostic Significance of MET Amplification and Expression in Gastric Cancer: A Systematic Review with Meta-Analysis
title_sort prognostic significance of met amplification and expression in gastric cancer: a systematic review with meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885582/
https://www.ncbi.nlm.nih.gov/pubmed/24416238
http://dx.doi.org/10.1371/journal.pone.0084502
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