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Correlation of DAPK1 methylation and the risk of gastrointestinal cancer: A systematic review and meta-analysis

OBJECTIVE: One of the critical mechanisms of gastrointestinal cancer pathogenesis is the silencing of death associated protein kinase 1 (DAPK1), which could be caused by aberrant methylation of the promoter. However, the relationship between DAPK1 methylation and the risk of gastrointestinal cancer...

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Autores principales: Yuan, Wenzheng, Chen, Jinhuang, Shu, Yan, Liu, Sanguang, Wu, Liang, Ji, Jintong, Liu, Zhengyi, Tang, Qiang, Zhou, Zili, Cheng, Yifeng, Jiang, Bin, Shu, Xiaogang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608298/
https://www.ncbi.nlm.nih.gov/pubmed/28934284
http://dx.doi.org/10.1371/journal.pone.0184959
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author Yuan, Wenzheng
Chen, Jinhuang
Shu, Yan
Liu, Sanguang
Wu, Liang
Ji, Jintong
Liu, Zhengyi
Tang, Qiang
Zhou, Zili
Cheng, Yifeng
Jiang, Bin
Shu, Xiaogang
author_facet Yuan, Wenzheng
Chen, Jinhuang
Shu, Yan
Liu, Sanguang
Wu, Liang
Ji, Jintong
Liu, Zhengyi
Tang, Qiang
Zhou, Zili
Cheng, Yifeng
Jiang, Bin
Shu, Xiaogang
author_sort Yuan, Wenzheng
collection PubMed
description OBJECTIVE: One of the critical mechanisms of gastrointestinal cancer pathogenesis is the silencing of death associated protein kinase 1 (DAPK1), which could be caused by aberrant methylation of the promoter. However, the relationship between DAPK1 methylation and the risk of gastrointestinal cancer is still controversial. Hence, we conducted this study to determine the potential correlation. METHODS: Eligible publications were searched in the Pubmed, Embase, and Cochrane Library through November 2016 according to the inclusion criteria and exclusion criteria. Revman 5.3 and Stata 12.0 software were used to analyze the relevant data regarding the association between the frequency of DAPK1 methylation and gastrointestinal cancer. RESULTS: A total of 22 studies with 2406 patients were included in this meta analysis. Methylation of DAPK1 was positively related with the risk of gastrointestinal cancer (odds ratio [OR] = 5.35, 95% confidence interval [CI]: 2.76–10.38, P<0.00001, random effects model). The source of heterogeneity was analyzed by sensitivity analysis and subgroup analysis. After omitting one heterogeneous study, the I(2) decreased and the OR increased in pooled analysis. Also, the heterogeneity decreased most significantly in the subgroup of studies that had a sample size of less than 60 cases. Then, the correlations between DAPK1 methylation and clinicopathological features of gastrointestinal cancer were assessed. DAPK1 methylation was positively correlated with the lymph node (N) stage (positive vs. negative, OR = 1.45, 95%CI: 1.01–2.06, P = 0.04, fixed effects model) and poor differentiation (OR = 1.55, 95%CI: 1.02–2.35, P = 0.04, fixed effects model) in gastric cancer, and the association was significant among Asian patients. However, among cases of gastrointestinal cancer, the association between DAPK1 methylation and tumor (T) stage, N stage, distant metastasis (M) stage, and cancer differentiation were not statistically significant. CONCLUSIONS: DAPK1 methylation is a potential biomarker for the early diagnosis of gastrointestinal cancer. Further analysis of the clinicopathological features indicated that aberrant methylation of DAPK1 is positively associated with the tumorigenesis of gastrointestinal cancer, and metastasis of gastric cancer.
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spelling pubmed-56082982017-10-09 Correlation of DAPK1 methylation and the risk of gastrointestinal cancer: A systematic review and meta-analysis Yuan, Wenzheng Chen, Jinhuang Shu, Yan Liu, Sanguang Wu, Liang Ji, Jintong Liu, Zhengyi Tang, Qiang Zhou, Zili Cheng, Yifeng Jiang, Bin Shu, Xiaogang PLoS One Research Article OBJECTIVE: One of the critical mechanisms of gastrointestinal cancer pathogenesis is the silencing of death associated protein kinase 1 (DAPK1), which could be caused by aberrant methylation of the promoter. However, the relationship between DAPK1 methylation and the risk of gastrointestinal cancer is still controversial. Hence, we conducted this study to determine the potential correlation. METHODS: Eligible publications were searched in the Pubmed, Embase, and Cochrane Library through November 2016 according to the inclusion criteria and exclusion criteria. Revman 5.3 and Stata 12.0 software were used to analyze the relevant data regarding the association between the frequency of DAPK1 methylation and gastrointestinal cancer. RESULTS: A total of 22 studies with 2406 patients were included in this meta analysis. Methylation of DAPK1 was positively related with the risk of gastrointestinal cancer (odds ratio [OR] = 5.35, 95% confidence interval [CI]: 2.76–10.38, P<0.00001, random effects model). The source of heterogeneity was analyzed by sensitivity analysis and subgroup analysis. After omitting one heterogeneous study, the I(2) decreased and the OR increased in pooled analysis. Also, the heterogeneity decreased most significantly in the subgroup of studies that had a sample size of less than 60 cases. Then, the correlations between DAPK1 methylation and clinicopathological features of gastrointestinal cancer were assessed. DAPK1 methylation was positively correlated with the lymph node (N) stage (positive vs. negative, OR = 1.45, 95%CI: 1.01–2.06, P = 0.04, fixed effects model) and poor differentiation (OR = 1.55, 95%CI: 1.02–2.35, P = 0.04, fixed effects model) in gastric cancer, and the association was significant among Asian patients. However, among cases of gastrointestinal cancer, the association between DAPK1 methylation and tumor (T) stage, N stage, distant metastasis (M) stage, and cancer differentiation were not statistically significant. CONCLUSIONS: DAPK1 methylation is a potential biomarker for the early diagnosis of gastrointestinal cancer. Further analysis of the clinicopathological features indicated that aberrant methylation of DAPK1 is positively associated with the tumorigenesis of gastrointestinal cancer, and metastasis of gastric cancer. Public Library of Science 2017-09-21 /pmc/articles/PMC5608298/ /pubmed/28934284 http://dx.doi.org/10.1371/journal.pone.0184959 Text en © 2017 Yuan 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Yuan, Wenzheng
Chen, Jinhuang
Shu, Yan
Liu, Sanguang
Wu, Liang
Ji, Jintong
Liu, Zhengyi
Tang, Qiang
Zhou, Zili
Cheng, Yifeng
Jiang, Bin
Shu, Xiaogang
Correlation of DAPK1 methylation and the risk of gastrointestinal cancer: A systematic review and meta-analysis
title Correlation of DAPK1 methylation and the risk of gastrointestinal cancer: A systematic review and meta-analysis
title_full Correlation of DAPK1 methylation and the risk of gastrointestinal cancer: A systematic review and meta-analysis
title_fullStr Correlation of DAPK1 methylation and the risk of gastrointestinal cancer: A systematic review and meta-analysis
title_full_unstemmed Correlation of DAPK1 methylation and the risk of gastrointestinal cancer: A systematic review and meta-analysis
title_short Correlation of DAPK1 methylation and the risk of gastrointestinal cancer: A systematic review and meta-analysis
title_sort correlation of dapk1 methylation and the risk of gastrointestinal cancer: a systematic review and meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608298/
https://www.ncbi.nlm.nih.gov/pubmed/28934284
http://dx.doi.org/10.1371/journal.pone.0184959
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