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Association between germline homeobox B13 (HOXB13) G84E allele and prostate cancer susceptibility: a meta-analysis and trial sequential analysis

Germline HOXB13 G84E mutation (rs138213197) has been described associated with prostate cancer (PCa) susceptibility but results of different studies are inconsistent. We conducted this meta-analysis to evaluate the specific role of this mutation. Relevant available studies were identified by searchi...

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Autores principales: Zhang, Jianzhong, Xiao, Li, Qin, Zhiqiang, Xu, Aiming, Zhao, Kai, Liang, Chao, Miao, Chenkui, Zhu, Jundong, Chen, Wei, Hua, Yibo, Liu, Yiyang, Zhang, Chao, Yu, Yajie, Su, Shifeng, Wang, Zengjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341860/
https://www.ncbi.nlm.nih.gov/pubmed/27626483
http://dx.doi.org/10.18632/oncotarget.11937
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author Zhang, Jianzhong
Xiao, Li
Qin, Zhiqiang
Xu, Aiming
Zhao, Kai
Liang, Chao
Miao, Chenkui
Zhu, Jundong
Chen, Wei
Hua, Yibo
Liu, Yiyang
Zhang, Chao
Yu, Yajie
Su, Shifeng
Wang, Zengjun
author_facet Zhang, Jianzhong
Xiao, Li
Qin, Zhiqiang
Xu, Aiming
Zhao, Kai
Liang, Chao
Miao, Chenkui
Zhu, Jundong
Chen, Wei
Hua, Yibo
Liu, Yiyang
Zhang, Chao
Yu, Yajie
Su, Shifeng
Wang, Zengjun
author_sort Zhang, Jianzhong
collection PubMed
description Germline HOXB13 G84E mutation (rs138213197) has been described associated with prostate cancer (PCa) susceptibility but results of different studies are inconsistent. We conducted this meta-analysis to evaluate the specific role of this mutation. Relevant available studies were identified by searching the databases Pubmed, Embase and Web of Science. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to measure the strength of the association. Subgroup analysis were performed to evaluate the specific role of rs138213197 in disease aggressiveness, diagnostic age and family history. Furthermore, trial sequential analysis (TSA) was conducted for the first time to estimate whether the evidence of the results is sufficient. Our results indicated that significant increased PCa susceptibility was associated with rs138213197 compared with non-carriers (OR = 3.38, 95% CI: 2.45–4.66). Besides, in subgroup analysis, HOXB13 G84E variant was obviously associated with early onset (OR = 2.90, 95% CI: 2.24–3.75), affected relatives (OR = 2.60, 95% CI 2.19–3.10) and highly aggressive disease (OR = 2.38, 95% CI 1.84–3.08). By TSA, the findings in the current study were based on sufficient evidence. Therefore, our results indicated that the G84E mutation in HOXB13 gene might increase susceptibility to PCa.
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spelling pubmed-53418602017-03-23 Association between germline homeobox B13 (HOXB13) G84E allele and prostate cancer susceptibility: a meta-analysis and trial sequential analysis Zhang, Jianzhong Xiao, Li Qin, Zhiqiang Xu, Aiming Zhao, Kai Liang, Chao Miao, Chenkui Zhu, Jundong Chen, Wei Hua, Yibo Liu, Yiyang Zhang, Chao Yu, Yajie Su, Shifeng Wang, Zengjun Oncotarget Research Paper Germline HOXB13 G84E mutation (rs138213197) has been described associated with prostate cancer (PCa) susceptibility but results of different studies are inconsistent. We conducted this meta-analysis to evaluate the specific role of this mutation. Relevant available studies were identified by searching the databases Pubmed, Embase and Web of Science. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to measure the strength of the association. Subgroup analysis were performed to evaluate the specific role of rs138213197 in disease aggressiveness, diagnostic age and family history. Furthermore, trial sequential analysis (TSA) was conducted for the first time to estimate whether the evidence of the results is sufficient. Our results indicated that significant increased PCa susceptibility was associated with rs138213197 compared with non-carriers (OR = 3.38, 95% CI: 2.45–4.66). Besides, in subgroup analysis, HOXB13 G84E variant was obviously associated with early onset (OR = 2.90, 95% CI: 2.24–3.75), affected relatives (OR = 2.60, 95% CI 2.19–3.10) and highly aggressive disease (OR = 2.38, 95% CI 1.84–3.08). By TSA, the findings in the current study were based on sufficient evidence. Therefore, our results indicated that the G84E mutation in HOXB13 gene might increase susceptibility to PCa. Impact Journals LLC 2016-09-10 /pmc/articles/PMC5341860/ /pubmed/27626483 http://dx.doi.org/10.18632/oncotarget.11937 Text en Copyright: © 2016 Zhang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Zhang, Jianzhong
Xiao, Li
Qin, Zhiqiang
Xu, Aiming
Zhao, Kai
Liang, Chao
Miao, Chenkui
Zhu, Jundong
Chen, Wei
Hua, Yibo
Liu, Yiyang
Zhang, Chao
Yu, Yajie
Su, Shifeng
Wang, Zengjun
Association between germline homeobox B13 (HOXB13) G84E allele and prostate cancer susceptibility: a meta-analysis and trial sequential analysis
title Association between germline homeobox B13 (HOXB13) G84E allele and prostate cancer susceptibility: a meta-analysis and trial sequential analysis
title_full Association between germline homeobox B13 (HOXB13) G84E allele and prostate cancer susceptibility: a meta-analysis and trial sequential analysis
title_fullStr Association between germline homeobox B13 (HOXB13) G84E allele and prostate cancer susceptibility: a meta-analysis and trial sequential analysis
title_full_unstemmed Association between germline homeobox B13 (HOXB13) G84E allele and prostate cancer susceptibility: a meta-analysis and trial sequential analysis
title_short Association between germline homeobox B13 (HOXB13) G84E allele and prostate cancer susceptibility: a meta-analysis and trial sequential analysis
title_sort association between germline homeobox b13 (hoxb13) g84e allele and prostate cancer susceptibility: a meta-analysis and trial sequential analysis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341860/
https://www.ncbi.nlm.nih.gov/pubmed/27626483
http://dx.doi.org/10.18632/oncotarget.11937
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