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The association between CDH1 promoter methylation and patients with ovarian cancer: a systematic meta-analysis

BACKGROUND: The down-regulation of E-cadherin gene (CDH1) expression has been regarded as an important event in cancer invasion and metastasis. However, the association between CDH1 promoter methylation and ovarian cancer remains unclear. A meta-analysis was conducted to evaluate the potential role...

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Autores principales: Wang, Qiang, Wang, Bing, Zhang, Yun-mei, Wang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827236/
https://www.ncbi.nlm.nih.gov/pubmed/27067410
http://dx.doi.org/10.1186/s13048-016-0231-1
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author Wang, Qiang
Wang, Bing
Zhang, Yun-mei
Wang, Wei
author_facet Wang, Qiang
Wang, Bing
Zhang, Yun-mei
Wang, Wei
author_sort Wang, Qiang
collection PubMed
description BACKGROUND: The down-regulation of E-cadherin gene (CDH1) expression has been regarded as an important event in cancer invasion and metastasis. However, the association between CDH1 promoter methylation and ovarian cancer remains unclear. A meta-analysis was conducted to evaluate the potential role of CDH1 promoter methylation in ovarian cancer. METHODS: Relevant articles were identified by searches of PubMed, EMBASE, Cochrane Library, CNKI and Wanfang databases. The pooled odds ratio (OR) and corresponding 95 % confidence interval (CI) were calculated to assess the strength of association. RESULTS: Nine studies were performed using the fixed-effects model in this study, including 485 cancer tissues and 255 nonmalignant tissues. The findings showed that CDH1 promoter methylation had an increased risk of ovarian cancer in cancer tissues (OR = 8.71, P < 0.001) in comparison with nonmalignant tissues. Subgroup analysis of the ethnicity showed that the OR value of CDH1 methylation in Asian population subgroup (OR = 13.20, P < 0.001) was higher than that in Caucasian population subgroup (OR = 3.84, P = 0.005). No significant association was found between ovarian cancer and low malignant potential (LMP) tumor (P = 0.096) among 2 studies, and between CDH1 promoter methylation and tumor stage and tumor histology (all P > 0.05). There was not any evidence of publication bias by Egger’s test (all P > 0.05). CONCLUSIONS: CDH1 promoter methylation can be a potential biomarker in ovarian cancer risk prediction, especially Asians can be more susceptible to CDH1 methylation. However, more studies are still done in the future.
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spelling pubmed-48272362016-04-12 The association between CDH1 promoter methylation and patients with ovarian cancer: a systematic meta-analysis Wang, Qiang Wang, Bing Zhang, Yun-mei Wang, Wei J Ovarian Res Research BACKGROUND: The down-regulation of E-cadherin gene (CDH1) expression has been regarded as an important event in cancer invasion and metastasis. However, the association between CDH1 promoter methylation and ovarian cancer remains unclear. A meta-analysis was conducted to evaluate the potential role of CDH1 promoter methylation in ovarian cancer. METHODS: Relevant articles were identified by searches of PubMed, EMBASE, Cochrane Library, CNKI and Wanfang databases. The pooled odds ratio (OR) and corresponding 95 % confidence interval (CI) were calculated to assess the strength of association. RESULTS: Nine studies were performed using the fixed-effects model in this study, including 485 cancer tissues and 255 nonmalignant tissues. The findings showed that CDH1 promoter methylation had an increased risk of ovarian cancer in cancer tissues (OR = 8.71, P < 0.001) in comparison with nonmalignant tissues. Subgroup analysis of the ethnicity showed that the OR value of CDH1 methylation in Asian population subgroup (OR = 13.20, P < 0.001) was higher than that in Caucasian population subgroup (OR = 3.84, P = 0.005). No significant association was found between ovarian cancer and low malignant potential (LMP) tumor (P = 0.096) among 2 studies, and between CDH1 promoter methylation and tumor stage and tumor histology (all P > 0.05). There was not any evidence of publication bias by Egger’s test (all P > 0.05). CONCLUSIONS: CDH1 promoter methylation can be a potential biomarker in ovarian cancer risk prediction, especially Asians can be more susceptible to CDH1 methylation. However, more studies are still done in the future. BioMed Central 2016-04-11 /pmc/articles/PMC4827236/ /pubmed/27067410 http://dx.doi.org/10.1186/s13048-016-0231-1 Text en © Wang et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wang, Qiang
Wang, Bing
Zhang, Yun-mei
Wang, Wei
The association between CDH1 promoter methylation and patients with ovarian cancer: a systematic meta-analysis
title The association between CDH1 promoter methylation and patients with ovarian cancer: a systematic meta-analysis
title_full The association between CDH1 promoter methylation and patients with ovarian cancer: a systematic meta-analysis
title_fullStr The association between CDH1 promoter methylation and patients with ovarian cancer: a systematic meta-analysis
title_full_unstemmed The association between CDH1 promoter methylation and patients with ovarian cancer: a systematic meta-analysis
title_short The association between CDH1 promoter methylation and patients with ovarian cancer: a systematic meta-analysis
title_sort association between cdh1 promoter methylation and patients with ovarian cancer: a systematic meta-analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827236/
https://www.ncbi.nlm.nih.gov/pubmed/27067410
http://dx.doi.org/10.1186/s13048-016-0231-1
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