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Meta-Analysis of the Prognostic Value of Smad4 Immunohistochemistry in Various Cancers

BACKGROUND: Accumulating evidence indicates that Smad4 (DPC4) plays a fundamental role in the development and prognosis of several types of cancer. The objective of this study was to conduct a meta-analysis to evaluate whether the loss of Smad4 staining could serve as a prognostic marker. METHODS: A...

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Autores principales: Du, Yiping, Zhou, Xin, Huang, Zebo, Qiu, Tianzhu, Wang, Jian, Zhu, Wei, Wang, Tongshan, Liu, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4198206/
https://www.ncbi.nlm.nih.gov/pubmed/25333693
http://dx.doi.org/10.1371/journal.pone.0110182
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author Du, Yiping
Zhou, Xin
Huang, Zebo
Qiu, Tianzhu
Wang, Jian
Zhu, Wei
Wang, Tongshan
Liu, Ping
author_facet Du, Yiping
Zhou, Xin
Huang, Zebo
Qiu, Tianzhu
Wang, Jian
Zhu, Wei
Wang, Tongshan
Liu, Ping
author_sort Du, Yiping
collection PubMed
description BACKGROUND: Accumulating evidence indicates that Smad4 (DPC4) plays a fundamental role in the development and prognosis of several types of cancer. The objective of this study was to conduct a meta-analysis to evaluate whether the loss of Smad4 staining could serve as a prognostic marker. METHODS: A comprehensive meta-analysis was conducted using major useful databases to determine the relationship between the immunohistochemical detection of Smad4 and the survival of patients with various cancers. We used hazard ratios (HRs) with 95% confidence interval (CIs) as the effect estimation to evaluate the association of Smad4 with overall survival (OS), cancer-specific survival (CSS) or recurrence-free survival (RFS). The relationship between the clinical characteristics of patients and Smad4 was also evaluated using the odds ratio (OR). RESULTS: A total of 7570 patients from 26 studies were included in the analysis. The pooled results showed that loss of Smad4 staining was a negative predictor of OS with an HR of 1.97 (95% CI: 1.55–2.51; P(heterogeneity)<0.001) and CSS/RFS (HR = 1.81; 95% CI: 1.30–2.54; P(heterogeneity)<0.001). In addition, loss of Smad4 staining was more likely to be found in older (OR = 1.69, 95% CI: 1.09–2.61; P(heterogeneity) = 0.648) colorectal cancer patients with a late tumor stage (OR = 2.31, 95% CI: 1.71–3.10; P(heterogeneity) = 0.218) and in gastric cancer patients with lymph node metastasis (OR = 2.11, 95% CI: 1.03–4.34; P(heterogeneity) = 0.038). CONCLUSION: Based on these results, our meta-analysis provided evidence that loss of Smad4 staining could act as an unfavorable biomarker in the prognosis of various cancers and should be used as a powerful tool in future clinical trials.
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spelling pubmed-41982062014-10-21 Meta-Analysis of the Prognostic Value of Smad4 Immunohistochemistry in Various Cancers Du, Yiping Zhou, Xin Huang, Zebo Qiu, Tianzhu Wang, Jian Zhu, Wei Wang, Tongshan Liu, Ping PLoS One Research Article BACKGROUND: Accumulating evidence indicates that Smad4 (DPC4) plays a fundamental role in the development and prognosis of several types of cancer. The objective of this study was to conduct a meta-analysis to evaluate whether the loss of Smad4 staining could serve as a prognostic marker. METHODS: A comprehensive meta-analysis was conducted using major useful databases to determine the relationship between the immunohistochemical detection of Smad4 and the survival of patients with various cancers. We used hazard ratios (HRs) with 95% confidence interval (CIs) as the effect estimation to evaluate the association of Smad4 with overall survival (OS), cancer-specific survival (CSS) or recurrence-free survival (RFS). The relationship between the clinical characteristics of patients and Smad4 was also evaluated using the odds ratio (OR). RESULTS: A total of 7570 patients from 26 studies were included in the analysis. The pooled results showed that loss of Smad4 staining was a negative predictor of OS with an HR of 1.97 (95% CI: 1.55–2.51; P(heterogeneity)<0.001) and CSS/RFS (HR = 1.81; 95% CI: 1.30–2.54; P(heterogeneity)<0.001). In addition, loss of Smad4 staining was more likely to be found in older (OR = 1.69, 95% CI: 1.09–2.61; P(heterogeneity) = 0.648) colorectal cancer patients with a late tumor stage (OR = 2.31, 95% CI: 1.71–3.10; P(heterogeneity) = 0.218) and in gastric cancer patients with lymph node metastasis (OR = 2.11, 95% CI: 1.03–4.34; P(heterogeneity) = 0.038). CONCLUSION: Based on these results, our meta-analysis provided evidence that loss of Smad4 staining could act as an unfavorable biomarker in the prognosis of various cancers and should be used as a powerful tool in future clinical trials. Public Library of Science 2014-10-15 /pmc/articles/PMC4198206/ /pubmed/25333693 http://dx.doi.org/10.1371/journal.pone.0110182 Text en © 2014 Du 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
Du, Yiping
Zhou, Xin
Huang, Zebo
Qiu, Tianzhu
Wang, Jian
Zhu, Wei
Wang, Tongshan
Liu, Ping
Meta-Analysis of the Prognostic Value of Smad4 Immunohistochemistry in Various Cancers
title Meta-Analysis of the Prognostic Value of Smad4 Immunohistochemistry in Various Cancers
title_full Meta-Analysis of the Prognostic Value of Smad4 Immunohistochemistry in Various Cancers
title_fullStr Meta-Analysis of the Prognostic Value of Smad4 Immunohistochemistry in Various Cancers
title_full_unstemmed Meta-Analysis of the Prognostic Value of Smad4 Immunohistochemistry in Various Cancers
title_short Meta-Analysis of the Prognostic Value of Smad4 Immunohistochemistry in Various Cancers
title_sort meta-analysis of the prognostic value of smad4 immunohistochemistry in various cancers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4198206/
https://www.ncbi.nlm.nih.gov/pubmed/25333693
http://dx.doi.org/10.1371/journal.pone.0110182
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