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Meta-analysis of the likelihood of FOXC2 expression in early- and late-stage tumors
BACKGROUND: Aberrations in the expression of the transcription factor forkhead box C2 (FOXC2) have been linked to a number of malignancies. Here, we characterized the relationship between FOXC2 and cancer progression by conducting a meta-analysis of studies that reported the frequency of FOXC2 expre...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161797/ https://www.ncbi.nlm.nih.gov/pubmed/30279969 http://dx.doi.org/10.18632/oncotarget.26087 |
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author | Kume, Tsutomu Shackour, Tarek |
author_facet | Kume, Tsutomu Shackour, Tarek |
author_sort | Kume, Tsutomu |
collection | PubMed |
description | BACKGROUND: Aberrations in the expression of the transcription factor forkhead box C2 (FOXC2) have been linked to a number of malignancies. Here, we characterized the relationship between FOXC2 and cancer progression by conducting a meta-analysis of studies that reported the frequency of FOXC2 expression in tumors of different stages (T1, T2, T3, T4). METHODS: Relevant articles were retrieved from the Medline database by searching for the terms “FOXC2” and “cancer”; then, the retrieved articles were reviewed individually, and studies that were of multivariate cohort design, evaluated FOXC2 expression via immunohistochemical staining, and assessed the relationship between FOXC2 expression and cancer T-stage were included in our meta-analysis. RESULTS: Our search terms identified 139 studies, 9 of which met all inclusion criteria. A total of 1433 tumor samples were evaluated in the 9 studies; 596 samples were from early-stage (T1-T2) tumors, and 838 were from late-stage (T3-T4) tumors. FOXC2 was expressed in 46.0% of all samples, in 32.4% of early-stage tumor samples, and in 55.6% of late-stage tumor samples. When calculated relative to early-stage samples, the pooled risk for FOXC2 expression in late-stage samples was 1.367 (95% CI = 1.103–1.695, p = 0.004). CONCLUSION: The results from our meta-analysis of 9 studies indicate that FOXC2 is 36.7% more likely to be expressed in late-stage tumors than in early-stage tumors. |
format | Online Article Text |
id | pubmed-6161797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-61617972018-10-02 Meta-analysis of the likelihood of FOXC2 expression in early- and late-stage tumors Kume, Tsutomu Shackour, Tarek Oncotarget Meta-Analysis BACKGROUND: Aberrations in the expression of the transcription factor forkhead box C2 (FOXC2) have been linked to a number of malignancies. Here, we characterized the relationship between FOXC2 and cancer progression by conducting a meta-analysis of studies that reported the frequency of FOXC2 expression in tumors of different stages (T1, T2, T3, T4). METHODS: Relevant articles were retrieved from the Medline database by searching for the terms “FOXC2” and “cancer”; then, the retrieved articles were reviewed individually, and studies that were of multivariate cohort design, evaluated FOXC2 expression via immunohistochemical staining, and assessed the relationship between FOXC2 expression and cancer T-stage were included in our meta-analysis. RESULTS: Our search terms identified 139 studies, 9 of which met all inclusion criteria. A total of 1433 tumor samples were evaluated in the 9 studies; 596 samples were from early-stage (T1-T2) tumors, and 838 were from late-stage (T3-T4) tumors. FOXC2 was expressed in 46.0% of all samples, in 32.4% of early-stage tumor samples, and in 55.6% of late-stage tumor samples. When calculated relative to early-stage samples, the pooled risk for FOXC2 expression in late-stage samples was 1.367 (95% CI = 1.103–1.695, p = 0.004). CONCLUSION: The results from our meta-analysis of 9 studies indicate that FOXC2 is 36.7% more likely to be expressed in late-stage tumors than in early-stage tumors. Impact Journals LLC 2018-09-07 /pmc/articles/PMC6161797/ /pubmed/30279969 http://dx.doi.org/10.18632/oncotarget.26087 Text en Copyright: © 2018 Kume and Shackour http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Meta-Analysis Kume, Tsutomu Shackour, Tarek Meta-analysis of the likelihood of FOXC2 expression in early- and late-stage tumors |
title | Meta-analysis of the likelihood of FOXC2 expression in early- and late-stage tumors |
title_full | Meta-analysis of the likelihood of FOXC2 expression in early- and late-stage tumors |
title_fullStr | Meta-analysis of the likelihood of FOXC2 expression in early- and late-stage tumors |
title_full_unstemmed | Meta-analysis of the likelihood of FOXC2 expression in early- and late-stage tumors |
title_short | Meta-analysis of the likelihood of FOXC2 expression in early- and late-stage tumors |
title_sort | meta-analysis of the likelihood of foxc2 expression in early- and late-stage tumors |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161797/ https://www.ncbi.nlm.nih.gov/pubmed/30279969 http://dx.doi.org/10.18632/oncotarget.26087 |
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