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Variants of MIR137HG Genes are Associated with Liver Cancer Risk in Chinese Li Population

BACKGROUND: Liver cancer (LC) is the sixth most common cancer and the second leading cause of cancer mortality worldwide, and its incidence rate is high in China. METHODS: In this study, we aimed to investigate the contribution of MIR137HG (MIR137 Host Gene) polymorphisms to LC risk in a case–contro...

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Autores principales: Wang, Chaoying, Zhuang, Xiaohong, Xu, Junnv, Dai, Zhisheng, Wu, Weixiong, Zhang, Chengsheng, Lin, Shu, Chen, Sehong, Lin, Haifeng, Tang, Wenjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7053808/
https://www.ncbi.nlm.nih.gov/pubmed/32184616
http://dx.doi.org/10.2147/OTT.S225669
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author Wang, Chaoying
Zhuang, Xiaohong
Xu, Junnv
Dai, Zhisheng
Wu, Weixiong
Zhang, Chengsheng
Lin, Shu
Chen, Sehong
Lin, Haifeng
Tang, Wenjun
author_facet Wang, Chaoying
Zhuang, Xiaohong
Xu, Junnv
Dai, Zhisheng
Wu, Weixiong
Zhang, Chengsheng
Lin, Shu
Chen, Sehong
Lin, Haifeng
Tang, Wenjun
author_sort Wang, Chaoying
collection PubMed
description BACKGROUND: Liver cancer (LC) is the sixth most common cancer and the second leading cause of cancer mortality worldwide, and its incidence rate is high in China. METHODS: In this study, we aimed to investigate the contribution of MIR137HG (MIR137 Host Gene) polymorphisms to LC risk in a case–control study with 432 LC patients and 430 healthy controls. A logistic recession model was used to evaluate the effects of candidate single nucleotide polymorphisms (SNPs) on LC risk. HaploReg v 4.1 database was conducted to predict the potential functionality of SNPs. RESULTS: The results revealed that rs17371457 and rs7554283 in the MIR137HG gene were correlated with an enhanced LC risk under the allele (P = 0.001 and P = 0.043, respectively) and genetic models (P < 0.05). When the sample was stratified by gender and age, statistically significant associations were found. Rs9440302, rs17371457 and rs7554283 were associated with an increased the risk of LC among individuals aged >55 years (P < 0.05); rs17371457 was related to higher LC risk in males (P < 0.05). Similarly, the haplotype AG constituted by rs12333983 and rs3735451 significantly increased LC risk in Chinese Li population (P = 0.043). Six SNPs distributed in MIR137HG were successfully predicted as regulatory SNPs with different biological functions. CONCLUSION: Our research firstly showed that MIR137HG gene polymorphisms were implicated in LC susceptibility among Chinese Li population.
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spelling pubmed-70538082020-03-17 Variants of MIR137HG Genes are Associated with Liver Cancer Risk in Chinese Li Population Wang, Chaoying Zhuang, Xiaohong Xu, Junnv Dai, Zhisheng Wu, Weixiong Zhang, Chengsheng Lin, Shu Chen, Sehong Lin, Haifeng Tang, Wenjun Onco Targets Ther Original Research BACKGROUND: Liver cancer (LC) is the sixth most common cancer and the second leading cause of cancer mortality worldwide, and its incidence rate is high in China. METHODS: In this study, we aimed to investigate the contribution of MIR137HG (MIR137 Host Gene) polymorphisms to LC risk in a case–control study with 432 LC patients and 430 healthy controls. A logistic recession model was used to evaluate the effects of candidate single nucleotide polymorphisms (SNPs) on LC risk. HaploReg v 4.1 database was conducted to predict the potential functionality of SNPs. RESULTS: The results revealed that rs17371457 and rs7554283 in the MIR137HG gene were correlated with an enhanced LC risk under the allele (P = 0.001 and P = 0.043, respectively) and genetic models (P < 0.05). When the sample was stratified by gender and age, statistically significant associations were found. Rs9440302, rs17371457 and rs7554283 were associated with an increased the risk of LC among individuals aged >55 years (P < 0.05); rs17371457 was related to higher LC risk in males (P < 0.05). Similarly, the haplotype AG constituted by rs12333983 and rs3735451 significantly increased LC risk in Chinese Li population (P = 0.043). Six SNPs distributed in MIR137HG were successfully predicted as regulatory SNPs with different biological functions. CONCLUSION: Our research firstly showed that MIR137HG gene polymorphisms were implicated in LC susceptibility among Chinese Li population. Dove 2020-02-28 /pmc/articles/PMC7053808/ /pubmed/32184616 http://dx.doi.org/10.2147/OTT.S225669 Text en © 2020 Wang et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Wang, Chaoying
Zhuang, Xiaohong
Xu, Junnv
Dai, Zhisheng
Wu, Weixiong
Zhang, Chengsheng
Lin, Shu
Chen, Sehong
Lin, Haifeng
Tang, Wenjun
Variants of MIR137HG Genes are Associated with Liver Cancer Risk in Chinese Li Population
title Variants of MIR137HG Genes are Associated with Liver Cancer Risk in Chinese Li Population
title_full Variants of MIR137HG Genes are Associated with Liver Cancer Risk in Chinese Li Population
title_fullStr Variants of MIR137HG Genes are Associated with Liver Cancer Risk in Chinese Li Population
title_full_unstemmed Variants of MIR137HG Genes are Associated with Liver Cancer Risk in Chinese Li Population
title_short Variants of MIR137HG Genes are Associated with Liver Cancer Risk in Chinese Li Population
title_sort variants of mir137hg genes are associated with liver cancer risk in chinese li population
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7053808/
https://www.ncbi.nlm.nih.gov/pubmed/32184616
http://dx.doi.org/10.2147/OTT.S225669
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