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Does hypermethylation of CpG island in the promoter region of the E‐cadherin gene increase the risk of lung cancer? A meta‐analysis

BACKGROUND: Hypermethylation of the CpG island in the promoter regions of tumor suppressor genes is common in the cancer tissue of non‐small cell lung cancer (NSCLC) patients. Epithelial cadherin (E‐cadherin) is a classic tumor suppressor gene of the cadherin superfamily and its promoter region is u...

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Autores principales: Sun, Zhenfeng, Liu, Gongzhe, Xu, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312839/
https://www.ncbi.nlm.nih.gov/pubmed/30390382
http://dx.doi.org/10.1111/1759-7714.12900
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author Sun, Zhenfeng
Liu, Gongzhe
Xu, Ning
author_facet Sun, Zhenfeng
Liu, Gongzhe
Xu, Ning
author_sort Sun, Zhenfeng
collection PubMed
description BACKGROUND: Hypermethylation of the CpG island in the promoter regions of tumor suppressor genes is common in the cancer tissue of non‐small cell lung cancer (NSCLC) patients. Epithelial cadherin (E‐cadherin) is a classic tumor suppressor gene of the cadherin superfamily and its promoter region is usually hypermethylated in malignant carcinomas. However, whether hypermethylation of the CpG island in the promoter region of E‐cadherin increases the risk of lung cancer is unknown. We conducted a meta‐analysis of E‐cadherin gene promoter methylation status in cancer tissue (CT) and autologous controls (AC). METHODS: Electronic databases were searched for E‐cadherin gene promoter methylation and NSCLC. The hypermethylation status between CT and AC of NSCLC patients were compared and pooled by random or fixed effect models according to statistical heterogeneity across the included studies. RESULTS: Eleven publications relevant to E‐cadherin gene promoter hypermethylation and lung cancer risk were identified and included. E‐cadherin gene promoter hypermethylation frequency in CT and AC was 0.32 (95% confidence interval [CI] 0.22–0.41) and 0.12 (95% CI 0.04–0.20), respectively, with statistical difference (P < 0.05). Significant statistical heterogeneity was found across the 11 studies (I(2) = 54.5, P < 0.05). The data was pooled through a random effect model with an odds ratio of 4.21 (95% CI 2.33–7.58) in CT compared to AC. CONCLUSION: The frequency of E‐cadherin promoter hypermethylation in CT is significantly higher than in AC, indicating that promoter hypermethylation of E‐cadherin plays an important role in NSCLC carcinogenesis.
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spelling pubmed-63128392019-01-07 Does hypermethylation of CpG island in the promoter region of the E‐cadherin gene increase the risk of lung cancer? A meta‐analysis Sun, Zhenfeng Liu, Gongzhe Xu, Ning Thorac Cancer Original Articles BACKGROUND: Hypermethylation of the CpG island in the promoter regions of tumor suppressor genes is common in the cancer tissue of non‐small cell lung cancer (NSCLC) patients. Epithelial cadherin (E‐cadherin) is a classic tumor suppressor gene of the cadherin superfamily and its promoter region is usually hypermethylated in malignant carcinomas. However, whether hypermethylation of the CpG island in the promoter region of E‐cadherin increases the risk of lung cancer is unknown. We conducted a meta‐analysis of E‐cadherin gene promoter methylation status in cancer tissue (CT) and autologous controls (AC). METHODS: Electronic databases were searched for E‐cadherin gene promoter methylation and NSCLC. The hypermethylation status between CT and AC of NSCLC patients were compared and pooled by random or fixed effect models according to statistical heterogeneity across the included studies. RESULTS: Eleven publications relevant to E‐cadherin gene promoter hypermethylation and lung cancer risk were identified and included. E‐cadherin gene promoter hypermethylation frequency in CT and AC was 0.32 (95% confidence interval [CI] 0.22–0.41) and 0.12 (95% CI 0.04–0.20), respectively, with statistical difference (P < 0.05). Significant statistical heterogeneity was found across the 11 studies (I(2) = 54.5, P < 0.05). The data was pooled through a random effect model with an odds ratio of 4.21 (95% CI 2.33–7.58) in CT compared to AC. CONCLUSION: The frequency of E‐cadherin promoter hypermethylation in CT is significantly higher than in AC, indicating that promoter hypermethylation of E‐cadherin plays an important role in NSCLC carcinogenesis. John Wiley & Sons Australia, Ltd 2018-11-03 2019-01 /pmc/articles/PMC6312839/ /pubmed/30390382 http://dx.doi.org/10.1111/1759-7714.12900 Text en © 2018 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Sun, Zhenfeng
Liu, Gongzhe
Xu, Ning
Does hypermethylation of CpG island in the promoter region of the E‐cadherin gene increase the risk of lung cancer? A meta‐analysis
title Does hypermethylation of CpG island in the promoter region of the E‐cadherin gene increase the risk of lung cancer? A meta‐analysis
title_full Does hypermethylation of CpG island in the promoter region of the E‐cadherin gene increase the risk of lung cancer? A meta‐analysis
title_fullStr Does hypermethylation of CpG island in the promoter region of the E‐cadherin gene increase the risk of lung cancer? A meta‐analysis
title_full_unstemmed Does hypermethylation of CpG island in the promoter region of the E‐cadherin gene increase the risk of lung cancer? A meta‐analysis
title_short Does hypermethylation of CpG island in the promoter region of the E‐cadherin gene increase the risk of lung cancer? A meta‐analysis
title_sort does hypermethylation of cpg island in the promoter region of the e‐cadherin gene increase the risk of lung cancer? a meta‐analysis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312839/
https://www.ncbi.nlm.nih.gov/pubmed/30390382
http://dx.doi.org/10.1111/1759-7714.12900
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