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Prognostic and Clinicopathological Significance of Survivin in Colorectal Cancer: A Meta-Analysis
Survivin/BIRC5 is a potentially interesting prognostic marker and therapeutic target in colorectal cancer (CRC). However, the available data on survivin expression in CRC are heterogeneous. Thus, to clarify the prognostic relevance of survivin in patients with CRC and its association with clinicopat...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670901/ https://www.ncbi.nlm.nih.gov/pubmed/23755220 http://dx.doi.org/10.1371/journal.pone.0065338 |
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author | Krieg, Andreas Werner, Thomas A. Verde, Pablo E. Stoecklein, Nikolas H. Knoefel, Wolfram T. |
author_facet | Krieg, Andreas Werner, Thomas A. Verde, Pablo E. Stoecklein, Nikolas H. Knoefel, Wolfram T. |
author_sort | Krieg, Andreas |
collection | PubMed |
description | Survivin/BIRC5 is a potentially interesting prognostic marker and therapeutic target in colorectal cancer (CRC). However, the available data on survivin expression in CRC are heterogeneous. Thus, to clarify the prognostic relevance of survivin in patients with CRC and its association with clinicopathological parameters we performed a meta-analysis. We screened PubMed and EMBASE for those studies that investigated the prognostic value of survivin and its association with clinicopathological parameters in CRC. Data from eligible studies were extracted and included into the meta-analyses using a random effects model. Electronical literature search identified 15 studies including 1934 patients with CRC mostly detecting survivin by immunohistochemistry (IHC). Pooled hazard ratios of 11 studies that performed survival analysis revealed a positive correlation between survivin expression and poor prognosis (HR 1.93; 95% CI: 1.55–2.42; P<0.00001; I(2) = 23%). Subgroup analyses with respect to the detection method, HR estimation, global quality score and the country of origin in which the study was conducted supported the stability of this observation. In addition, meta-analyses revealed a significant association between expression of survivin and the presence of lymph node metastases (OR: 0.37; 95% CI: 0.19–0.75; I(2) = 61%) or blood vessel invasion (OR: 0.50; 95% CI: 0.28–0.90; I(2) = 0%). Expression of survivin indicates poor prognosis and a pro-metastatic phenotype and may be useful in identifying a subgroup of patients that could benefit from a targeted therapy against survivin in CRC. |
format | Online Article Text |
id | pubmed-3670901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36709012013-06-10 Prognostic and Clinicopathological Significance of Survivin in Colorectal Cancer: A Meta-Analysis Krieg, Andreas Werner, Thomas A. Verde, Pablo E. Stoecklein, Nikolas H. Knoefel, Wolfram T. PLoS One Research Article Survivin/BIRC5 is a potentially interesting prognostic marker and therapeutic target in colorectal cancer (CRC). However, the available data on survivin expression in CRC are heterogeneous. Thus, to clarify the prognostic relevance of survivin in patients with CRC and its association with clinicopathological parameters we performed a meta-analysis. We screened PubMed and EMBASE for those studies that investigated the prognostic value of survivin and its association with clinicopathological parameters in CRC. Data from eligible studies were extracted and included into the meta-analyses using a random effects model. Electronical literature search identified 15 studies including 1934 patients with CRC mostly detecting survivin by immunohistochemistry (IHC). Pooled hazard ratios of 11 studies that performed survival analysis revealed a positive correlation between survivin expression and poor prognosis (HR 1.93; 95% CI: 1.55–2.42; P<0.00001; I(2) = 23%). Subgroup analyses with respect to the detection method, HR estimation, global quality score and the country of origin in which the study was conducted supported the stability of this observation. In addition, meta-analyses revealed a significant association between expression of survivin and the presence of lymph node metastases (OR: 0.37; 95% CI: 0.19–0.75; I(2) = 61%) or blood vessel invasion (OR: 0.50; 95% CI: 0.28–0.90; I(2) = 0%). Expression of survivin indicates poor prognosis and a pro-metastatic phenotype and may be useful in identifying a subgroup of patients that could benefit from a targeted therapy against survivin in CRC. Public Library of Science 2013-06-03 /pmc/articles/PMC3670901/ /pubmed/23755220 http://dx.doi.org/10.1371/journal.pone.0065338 Text en © 2013 Krieg 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 Krieg, Andreas Werner, Thomas A. Verde, Pablo E. Stoecklein, Nikolas H. Knoefel, Wolfram T. Prognostic and Clinicopathological Significance of Survivin in Colorectal Cancer: A Meta-Analysis |
title | Prognostic and Clinicopathological Significance of Survivin in Colorectal Cancer: A Meta-Analysis |
title_full | Prognostic and Clinicopathological Significance of Survivin in Colorectal Cancer: A Meta-Analysis |
title_fullStr | Prognostic and Clinicopathological Significance of Survivin in Colorectal Cancer: A Meta-Analysis |
title_full_unstemmed | Prognostic and Clinicopathological Significance of Survivin in Colorectal Cancer: A Meta-Analysis |
title_short | Prognostic and Clinicopathological Significance of Survivin in Colorectal Cancer: A Meta-Analysis |
title_sort | prognostic and clinicopathological significance of survivin in colorectal cancer: a meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670901/ https://www.ncbi.nlm.nih.gov/pubmed/23755220 http://dx.doi.org/10.1371/journal.pone.0065338 |
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