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Correlation of DEPDC5 rs1012068 and rs5998152 Polymorphisms with Risk of Hepatocellular Carcinoma: A Systematic Review and Meta-Analysis

BACKGROUND: Emerging evidence has shown that two common genetic polymorphisms within the pleckstrin domain-containing protein 5 (DEPDC5), rs1012068 and rs5998152, may be associated with the risk of hepatocellular carcinoma (HCC), especially in those individuals chronically infected with the hepatiti...

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Autores principales: Zhu, Shaoliang, Tang, Zhenyong, Zou, Mengjie, Tan, Tingting, Tang, Yi, Chen, Yuanyuan, Liang, Bin, Xie, Dongyi, Yang, Yongyu, Xie, Shaowei, Xie, Guangyuan, Dong, Xiaofeng, Liu, Tianqi, Tang, Yuntian, Yang, Jianrong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889158/
https://www.ncbi.nlm.nih.gov/pubmed/36733671
http://dx.doi.org/10.1155/2023/5957481
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author Zhu, Shaoliang
Tang, Zhenyong
Zou, Mengjie
Tan, Tingting
Tang, Yi
Chen, Yuanyuan
Liang, Bin
Xie, Dongyi
Yang, Yongyu
Xie, Shaowei
Xie, Guangyuan
Dong, Xiaofeng
Liu, Tianqi
Tang, Yuntian
Yang, Jianrong
author_facet Zhu, Shaoliang
Tang, Zhenyong
Zou, Mengjie
Tan, Tingting
Tang, Yi
Chen, Yuanyuan
Liang, Bin
Xie, Dongyi
Yang, Yongyu
Xie, Shaowei
Xie, Guangyuan
Dong, Xiaofeng
Liu, Tianqi
Tang, Yuntian
Yang, Jianrong
author_sort Zhu, Shaoliang
collection PubMed
description BACKGROUND: Emerging evidence has shown that two common genetic polymorphisms within the pleckstrin domain-containing protein 5 (DEPDC5), rs1012068 and rs5998152, may be associated with the risk of hepatocellular carcinoma (HCC), especially in those individuals chronically infected with the hepatitis C virus (HCV) or the hepatitis B virus (HBV). However, these findings have not been consistently replicated in the literature due to limited sample sizes or different etiologies of HCC. Thus, the present systematic review and meta-analysis were performed to resolve this inconsistency. METHODS: The databases PubMed, Embase, Web of Science, the China National Knowledge Infrastructure, and Scopus were searched up to December 12, 2022. Data from relevant studies were pooled, and odds ratios and 95% confidence intervals were calculated. RESULTS: A total of 11 case-control studies encompassing 2,609 cases and 8,171 controls on rs1012068 and three encompassing 411 cases and 1,448 controls on rs5998152 were included. Results indicated that the DEPDC5 rs1012068 polymorphism did not significantly increase HCC risk in the total population (allelic model (OR = 1.32, 95% CI = 1.04–1.67, P = 0.02); the recessive model (OR = 1.42, 95% CI = 0.96–2.10, P = 0.08); the dominant model (OR = 1.43, 95% CI = 1.09–1.87, P = 0.01); the homozygous model (OR = 1.61, 95% CI = 1.01–2.57, P = 0.05); the heterozygous model (OR = 1.39, 95% CI = 1.09–1.79, P = 0.009)). Subgroup analyses based on ethnicity and etiology revealed that the rs1012068 polymorphism, under all five genetic models, was associated with increased HCC risk in Asians or in individuals with chronic HBV infection but not in individuals with chronic HCV infection. A significant association was also observed between rs5998152 and HCV-related HCC risk in Asians chronically infected with HCV under allelic, dominant, and heterozygous models. CONCLUSION: Our study suggests that the DEPDC5 rs1012068 polymorphism increases HCC risk, especially in Asians with chronic HBV infection, while the rs5998152 polymorphism increases HCC risk in Asians with chronic HCV infection.
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spelling pubmed-98891582023-02-01 Correlation of DEPDC5 rs1012068 and rs5998152 Polymorphisms with Risk of Hepatocellular Carcinoma: A Systematic Review and Meta-Analysis Zhu, Shaoliang Tang, Zhenyong Zou, Mengjie Tan, Tingting Tang, Yi Chen, Yuanyuan Liang, Bin Xie, Dongyi Yang, Yongyu Xie, Shaowei Xie, Guangyuan Dong, Xiaofeng Liu, Tianqi Tang, Yuntian Yang, Jianrong J Oncol Review Article BACKGROUND: Emerging evidence has shown that two common genetic polymorphisms within the pleckstrin domain-containing protein 5 (DEPDC5), rs1012068 and rs5998152, may be associated with the risk of hepatocellular carcinoma (HCC), especially in those individuals chronically infected with the hepatitis C virus (HCV) or the hepatitis B virus (HBV). However, these findings have not been consistently replicated in the literature due to limited sample sizes or different etiologies of HCC. Thus, the present systematic review and meta-analysis were performed to resolve this inconsistency. METHODS: The databases PubMed, Embase, Web of Science, the China National Knowledge Infrastructure, and Scopus were searched up to December 12, 2022. Data from relevant studies were pooled, and odds ratios and 95% confidence intervals were calculated. RESULTS: A total of 11 case-control studies encompassing 2,609 cases and 8,171 controls on rs1012068 and three encompassing 411 cases and 1,448 controls on rs5998152 were included. Results indicated that the DEPDC5 rs1012068 polymorphism did not significantly increase HCC risk in the total population (allelic model (OR = 1.32, 95% CI = 1.04–1.67, P = 0.02); the recessive model (OR = 1.42, 95% CI = 0.96–2.10, P = 0.08); the dominant model (OR = 1.43, 95% CI = 1.09–1.87, P = 0.01); the homozygous model (OR = 1.61, 95% CI = 1.01–2.57, P = 0.05); the heterozygous model (OR = 1.39, 95% CI = 1.09–1.79, P = 0.009)). Subgroup analyses based on ethnicity and etiology revealed that the rs1012068 polymorphism, under all five genetic models, was associated with increased HCC risk in Asians or in individuals with chronic HBV infection but not in individuals with chronic HCV infection. A significant association was also observed between rs5998152 and HCV-related HCC risk in Asians chronically infected with HCV under allelic, dominant, and heterozygous models. CONCLUSION: Our study suggests that the DEPDC5 rs1012068 polymorphism increases HCC risk, especially in Asians with chronic HBV infection, while the rs5998152 polymorphism increases HCC risk in Asians with chronic HCV infection. Hindawi 2023-01-24 /pmc/articles/PMC9889158/ /pubmed/36733671 http://dx.doi.org/10.1155/2023/5957481 Text en Copyright © 2023 Shaoliang Zhu et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Zhu, Shaoliang
Tang, Zhenyong
Zou, Mengjie
Tan, Tingting
Tang, Yi
Chen, Yuanyuan
Liang, Bin
Xie, Dongyi
Yang, Yongyu
Xie, Shaowei
Xie, Guangyuan
Dong, Xiaofeng
Liu, Tianqi
Tang, Yuntian
Yang, Jianrong
Correlation of DEPDC5 rs1012068 and rs5998152 Polymorphisms with Risk of Hepatocellular Carcinoma: A Systematic Review and Meta-Analysis
title Correlation of DEPDC5 rs1012068 and rs5998152 Polymorphisms with Risk of Hepatocellular Carcinoma: A Systematic Review and Meta-Analysis
title_full Correlation of DEPDC5 rs1012068 and rs5998152 Polymorphisms with Risk of Hepatocellular Carcinoma: A Systematic Review and Meta-Analysis
title_fullStr Correlation of DEPDC5 rs1012068 and rs5998152 Polymorphisms with Risk of Hepatocellular Carcinoma: A Systematic Review and Meta-Analysis
title_full_unstemmed Correlation of DEPDC5 rs1012068 and rs5998152 Polymorphisms with Risk of Hepatocellular Carcinoma: A Systematic Review and Meta-Analysis
title_short Correlation of DEPDC5 rs1012068 and rs5998152 Polymorphisms with Risk of Hepatocellular Carcinoma: A Systematic Review and Meta-Analysis
title_sort correlation of depdc5 rs1012068 and rs5998152 polymorphisms with risk of hepatocellular carcinoma: a systematic review and meta-analysis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889158/
https://www.ncbi.nlm.nih.gov/pubmed/36733671
http://dx.doi.org/10.1155/2023/5957481
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