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Association between four common microRNA polymorphisms and the risk of hepatocellular carcinoma and HBV infection
microRNAs (miR/miRNAs) have been demonstrated to function as tumor suppressors and oncogenes, and miRNA polymorphisms may have a role in cancer development. The present study aimed to investigate the association between the miR-146aG>C, miR-149C>T, miR-196a2C>T and miR-499A>G polymorphis...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4114578/ https://www.ncbi.nlm.nih.gov/pubmed/25120701 http://dx.doi.org/10.3892/ol.2014.2257 |
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author | KOU, JIAN-TAO FAN, HUA HAN, DONGDONG LI, LIXIN LI, PING ZHU, JIQIAO MA, JUN ZHANG, ZHI-HUA HE, QIANG |
author_facet | KOU, JIAN-TAO FAN, HUA HAN, DONGDONG LI, LIXIN LI, PING ZHU, JIQIAO MA, JUN ZHANG, ZHI-HUA HE, QIANG |
author_sort | KOU, JIAN-TAO |
collection | PubMed |
description | microRNAs (miR/miRNAs) have been demonstrated to function as tumor suppressors and oncogenes, and miRNA polymorphisms may have a role in cancer development. The present study aimed to investigate the association between the miR-146aG>C, miR-149C>T, miR-196a2C>T and miR-499A>G polymorphisms and the risk of hepatocellular carcinoma (HCC) and hepatitis B virus (HBV) infection. A total of 271 patients with HCC and 532 healthy control participants were enrolled in the present study. miR-146aG>C, miR-149C>T, miR-196a2C>T and miR-499A>G polymorphisms were genotyped using the polymerase chain reaction-restriction fragment length polymorphism method. A significant difference was identified in the genotype frequency of miR-196a2C>T in the patients in the case group compared with the control group (χ(2)=6.88; P=0.032). Compared with the CC genotype, the miR-196a2 TT genotype was associated with a significantly reduced risk of HCC [odds ratio (OR), 0.62; 95% confidence interval (CI), 0.38–0.99], and a significantly reduced risk was also found in the dominant (OR, 0.69; 95% CI, 0.49–0.98) and recessive (OR, 0.70; 95% CI, 0.46–1.02) models. Moreover, individuals with HBV who were carrying the miR-196a2 CT and TT genotypes had a significantly reduced risk of HCC (OR, 0.62; 95% CI, 0.41–0.95; and OR, 0.39; 95% CI, 0.20–0.73, respectively). In conclusion, the present study found that the miR-196a2C>T polymorphism has a protective effect in patients with HCC, particularly in those with HBV infection. |
format | Online Article Text |
id | pubmed-4114578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-41145782014-08-12 Association between four common microRNA polymorphisms and the risk of hepatocellular carcinoma and HBV infection KOU, JIAN-TAO FAN, HUA HAN, DONGDONG LI, LIXIN LI, PING ZHU, JIQIAO MA, JUN ZHANG, ZHI-HUA HE, QIANG Oncol Lett Articles microRNAs (miR/miRNAs) have been demonstrated to function as tumor suppressors and oncogenes, and miRNA polymorphisms may have a role in cancer development. The present study aimed to investigate the association between the miR-146aG>C, miR-149C>T, miR-196a2C>T and miR-499A>G polymorphisms and the risk of hepatocellular carcinoma (HCC) and hepatitis B virus (HBV) infection. A total of 271 patients with HCC and 532 healthy control participants were enrolled in the present study. miR-146aG>C, miR-149C>T, miR-196a2C>T and miR-499A>G polymorphisms were genotyped using the polymerase chain reaction-restriction fragment length polymorphism method. A significant difference was identified in the genotype frequency of miR-196a2C>T in the patients in the case group compared with the control group (χ(2)=6.88; P=0.032). Compared with the CC genotype, the miR-196a2 TT genotype was associated with a significantly reduced risk of HCC [odds ratio (OR), 0.62; 95% confidence interval (CI), 0.38–0.99], and a significantly reduced risk was also found in the dominant (OR, 0.69; 95% CI, 0.49–0.98) and recessive (OR, 0.70; 95% CI, 0.46–1.02) models. Moreover, individuals with HBV who were carrying the miR-196a2 CT and TT genotypes had a significantly reduced risk of HCC (OR, 0.62; 95% CI, 0.41–0.95; and OR, 0.39; 95% CI, 0.20–0.73, respectively). In conclusion, the present study found that the miR-196a2C>T polymorphism has a protective effect in patients with HCC, particularly in those with HBV infection. D.A. Spandidos 2014-09 2014-06-16 /pmc/articles/PMC4114578/ /pubmed/25120701 http://dx.doi.org/10.3892/ol.2014.2257 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles KOU, JIAN-TAO FAN, HUA HAN, DONGDONG LI, LIXIN LI, PING ZHU, JIQIAO MA, JUN ZHANG, ZHI-HUA HE, QIANG Association between four common microRNA polymorphisms and the risk of hepatocellular carcinoma and HBV infection |
title | Association between four common microRNA polymorphisms and the risk of hepatocellular carcinoma and HBV infection |
title_full | Association between four common microRNA polymorphisms and the risk of hepatocellular carcinoma and HBV infection |
title_fullStr | Association between four common microRNA polymorphisms and the risk of hepatocellular carcinoma and HBV infection |
title_full_unstemmed | Association between four common microRNA polymorphisms and the risk of hepatocellular carcinoma and HBV infection |
title_short | Association between four common microRNA polymorphisms and the risk of hepatocellular carcinoma and HBV infection |
title_sort | association between four common microrna polymorphisms and the risk of hepatocellular carcinoma and hbv infection |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4114578/ https://www.ncbi.nlm.nih.gov/pubmed/25120701 http://dx.doi.org/10.3892/ol.2014.2257 |
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