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Meta-analysis of association between rs1447295 polymorphism and prostate cancer susceptibility

AIMS: A number of studies have found that the single nucleotide polymorphisms (SNPs) within the 8q24 region of genome were associated with the susceptibility of prostate cancer. Association between 8q24 SNP variant rs1447295 and higher risk of prostate cancer had been investigated, but those studies...

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Autores principales: Zhou, Juan, Yu, Yang, Zhu, Anyou, Wang, Fengchao, Kang, Shuxia, Pei, Yunfeng, Cao, Chunping, Ding, Chen, Wang, Duping, Sun, Li, Niu, Guoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5620154/
https://www.ncbi.nlm.nih.gov/pubmed/28978014
http://dx.doi.org/10.18632/oncotarget.17627
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author Zhou, Juan
Yu, Yang
Zhu, Anyou
Wang, Fengchao
Kang, Shuxia
Pei, Yunfeng
Cao, Chunping
Ding, Chen
Wang, Duping
Sun, Li
Niu, Guoping
author_facet Zhou, Juan
Yu, Yang
Zhu, Anyou
Wang, Fengchao
Kang, Shuxia
Pei, Yunfeng
Cao, Chunping
Ding, Chen
Wang, Duping
Sun, Li
Niu, Guoping
author_sort Zhou, Juan
collection PubMed
description AIMS: A number of studies have found that the single nucleotide polymorphisms (SNPs) within the 8q24 region of genome were associated with the susceptibility of prostate cancer. Association between 8q24 SNP variant rs1447295 and higher risk of prostate cancer had been investigated, but those studies were incomplete and the conclusions were obscure. METHODS: To better elucidate the relationship between rs1447295 polymorphism and the susceptibility of prostate cancer, we performed a more comprehensive meta-analysis about the association between rs1447295 polymorphism and prostate cancer susceptibility by collecting relevant articles published up to November, 2016 and excluding many replicated cohort data existing in previous reports, which made the conclusion more reliant and objective. RESULTS: The results showed that there was a significant prostate cancer risk associated with rs1447295 polymorphism not only in the total groups, but also in American, European and Asian descent subgroups. Meanwhile, a comprehensive analysis about the association between rs1447295 polymorphism and prostate cancer risk were conducted by using different clinical characteristic stratifications including Gleason score, tumor stage and PSA level. The result showed that rs1447295 polymorphism was correlated with different stages of prostate cancer CONCLUSIONS: There are strong association between rs1447295 polymorphism and prostate cancer susceptibility in different ethnic groups and different prostate cancer stage, suggesting that rs1447295 might serve as a reliable biomarker for prostate cancer diagnosis.
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spelling pubmed-56201542017-10-03 Meta-analysis of association between rs1447295 polymorphism and prostate cancer susceptibility Zhou, Juan Yu, Yang Zhu, Anyou Wang, Fengchao Kang, Shuxia Pei, Yunfeng Cao, Chunping Ding, Chen Wang, Duping Sun, Li Niu, Guoping Oncotarget Research Paper AIMS: A number of studies have found that the single nucleotide polymorphisms (SNPs) within the 8q24 region of genome were associated with the susceptibility of prostate cancer. Association between 8q24 SNP variant rs1447295 and higher risk of prostate cancer had been investigated, but those studies were incomplete and the conclusions were obscure. METHODS: To better elucidate the relationship between rs1447295 polymorphism and the susceptibility of prostate cancer, we performed a more comprehensive meta-analysis about the association between rs1447295 polymorphism and prostate cancer susceptibility by collecting relevant articles published up to November, 2016 and excluding many replicated cohort data existing in previous reports, which made the conclusion more reliant and objective. RESULTS: The results showed that there was a significant prostate cancer risk associated with rs1447295 polymorphism not only in the total groups, but also in American, European and Asian descent subgroups. Meanwhile, a comprehensive analysis about the association between rs1447295 polymorphism and prostate cancer risk were conducted by using different clinical characteristic stratifications including Gleason score, tumor stage and PSA level. The result showed that rs1447295 polymorphism was correlated with different stages of prostate cancer CONCLUSIONS: There are strong association between rs1447295 polymorphism and prostate cancer susceptibility in different ethnic groups and different prostate cancer stage, suggesting that rs1447295 might serve as a reliable biomarker for prostate cancer diagnosis. Impact Journals LLC 2017-05-05 /pmc/articles/PMC5620154/ /pubmed/28978014 http://dx.doi.org/10.18632/oncotarget.17627 Text en Copyright: © 2017 Zhou et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Zhou, Juan
Yu, Yang
Zhu, Anyou
Wang, Fengchao
Kang, Shuxia
Pei, Yunfeng
Cao, Chunping
Ding, Chen
Wang, Duping
Sun, Li
Niu, Guoping
Meta-analysis of association between rs1447295 polymorphism and prostate cancer susceptibility
title Meta-analysis of association between rs1447295 polymorphism and prostate cancer susceptibility
title_full Meta-analysis of association between rs1447295 polymorphism and prostate cancer susceptibility
title_fullStr Meta-analysis of association between rs1447295 polymorphism and prostate cancer susceptibility
title_full_unstemmed Meta-analysis of association between rs1447295 polymorphism and prostate cancer susceptibility
title_short Meta-analysis of association between rs1447295 polymorphism and prostate cancer susceptibility
title_sort meta-analysis of association between rs1447295 polymorphism and prostate cancer susceptibility
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5620154/
https://www.ncbi.nlm.nih.gov/pubmed/28978014
http://dx.doi.org/10.18632/oncotarget.17627
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