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Meta-analysis of the association between APC promoter methylation and colorectal cancer

Previous studies investigating the association between adenomatous polyposis coli (APC) gene promoter methylation and colorectal cancer (CRC) have yielded conflicting results. The aim of this study was to comprehensively evaluate the potential application of the detection of APC promoter methylation...

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Autores principales: Ding, Zhenyu, Jiang, Tong, Piao, Ying, Han, Tao, Han, Yaling, Xie, Xiaodong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4304602/
https://www.ncbi.nlm.nih.gov/pubmed/25632237
http://dx.doi.org/10.2147/OTT.S75827
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author Ding, Zhenyu
Jiang, Tong
Piao, Ying
Han, Tao
Han, Yaling
Xie, Xiaodong
author_facet Ding, Zhenyu
Jiang, Tong
Piao, Ying
Han, Tao
Han, Yaling
Xie, Xiaodong
author_sort Ding, Zhenyu
collection PubMed
description Previous studies investigating the association between adenomatous polyposis coli (APC) gene promoter methylation and colorectal cancer (CRC) have yielded conflicting results. The aim of this study was to comprehensively evaluate the potential application of the detection of APC promoter methylation to the prevention and treatment of CRC. PubMed, Embase, and MEDLINE (results updated to October 2014) were searched for relevant studies. The effect size was defined as the weighted odds ratio (OR), which was calculated using either the fixed-effects or random-effects model. Prespecified subgroup and sensitivity analyses were conducted to evaluate potential heterogeneity among the included studies. Nineteen studies comprising 2,426 participants were selected for our meta-analysis. The pooled results of nine studies comprising a total of 740 subjects indicated that APC promoter methylation was significantly associated with CRC risk (pooled OR 5.53; 95% confidence interval [CI] 3.50–8.76; P<0.01). Eleven studies with a total of 1,219 patients evaluated the association between APC promoter methylation and the presence of CRC metastasis, and the pooled OR was 0.80 (95% CI 0.44–1.46; P=0.47). A meta-analysis conducted with four studies with a total of 467 patients found no significant correlation between APC promoter methylation and the presence of colorectal adenoma (pooled OR 1.85; 95% CI 0.67–5.10; P=0.23). No significant correlation between APC promoter methylation and patients’ Dukes’ stage, TNM stage, differentiation grade, age, or sex was identified. In conclusion, APC promoter methylation was found to be significantly associated with a higher risk of developing CRC. The findings indicate that APC promoter methylation may be a potential biomarker for the carcinogenesis of CRC.
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spelling pubmed-43046022015-01-28 Meta-analysis of the association between APC promoter methylation and colorectal cancer Ding, Zhenyu Jiang, Tong Piao, Ying Han, Tao Han, Yaling Xie, Xiaodong Onco Targets Ther Original Research Previous studies investigating the association between adenomatous polyposis coli (APC) gene promoter methylation and colorectal cancer (CRC) have yielded conflicting results. The aim of this study was to comprehensively evaluate the potential application of the detection of APC promoter methylation to the prevention and treatment of CRC. PubMed, Embase, and MEDLINE (results updated to October 2014) were searched for relevant studies. The effect size was defined as the weighted odds ratio (OR), which was calculated using either the fixed-effects or random-effects model. Prespecified subgroup and sensitivity analyses were conducted to evaluate potential heterogeneity among the included studies. Nineteen studies comprising 2,426 participants were selected for our meta-analysis. The pooled results of nine studies comprising a total of 740 subjects indicated that APC promoter methylation was significantly associated with CRC risk (pooled OR 5.53; 95% confidence interval [CI] 3.50–8.76; P<0.01). Eleven studies with a total of 1,219 patients evaluated the association between APC promoter methylation and the presence of CRC metastasis, and the pooled OR was 0.80 (95% CI 0.44–1.46; P=0.47). A meta-analysis conducted with four studies with a total of 467 patients found no significant correlation between APC promoter methylation and the presence of colorectal adenoma (pooled OR 1.85; 95% CI 0.67–5.10; P=0.23). No significant correlation between APC promoter methylation and patients’ Dukes’ stage, TNM stage, differentiation grade, age, or sex was identified. In conclusion, APC promoter methylation was found to be significantly associated with a higher risk of developing CRC. The findings indicate that APC promoter methylation may be a potential biomarker for the carcinogenesis of CRC. Dove Medical Press 2015-01-19 /pmc/articles/PMC4304602/ /pubmed/25632237 http://dx.doi.org/10.2147/OTT.S75827 Text en © 2015 Ding et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Ding, Zhenyu
Jiang, Tong
Piao, Ying
Han, Tao
Han, Yaling
Xie, Xiaodong
Meta-analysis of the association between APC promoter methylation and colorectal cancer
title Meta-analysis of the association between APC promoter methylation and colorectal cancer
title_full Meta-analysis of the association between APC promoter methylation and colorectal cancer
title_fullStr Meta-analysis of the association between APC promoter methylation and colorectal cancer
title_full_unstemmed Meta-analysis of the association between APC promoter methylation and colorectal cancer
title_short Meta-analysis of the association between APC promoter methylation and colorectal cancer
title_sort meta-analysis of the association between apc promoter methylation and colorectal cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4304602/
https://www.ncbi.nlm.nih.gov/pubmed/25632237
http://dx.doi.org/10.2147/OTT.S75827
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