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Human leukocyte antigen gene polymorphisms are associated with systemic inflammation in hepatitis B virus-related hepatocellular carcinoma

BACKGROUND: Systemic inflammation (SI) is associated with tumor progression and overall survival (OS) in patients with hepatocellular carcinoma (HCC). The presence of some single nucleotide polymorphisms (SNPs) in the human leukocyte antigen (HLA) region can influence the prognosis of patients with...

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Autores principales: Wu, Xiao-long, Li, Zhi-yu, Bi, Xin-yu, Zhao, Hong, Zhao, Jian-jun, Zhou, Jian-guo, Han, Yue, Huang, Zhen, Zhang, Ye-fan, Cai, Jian-qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074760/
https://www.ncbi.nlm.nih.gov/pubmed/30104900
http://dx.doi.org/10.2147/CMAR.S167574
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author Wu, Xiao-long
Li, Zhi-yu
Bi, Xin-yu
Zhao, Hong
Zhao, Jian-jun
Zhou, Jian-guo
Han, Yue
Huang, Zhen
Zhang, Ye-fan
Cai, Jian-qiang
author_facet Wu, Xiao-long
Li, Zhi-yu
Bi, Xin-yu
Zhao, Hong
Zhao, Jian-jun
Zhou, Jian-guo
Han, Yue
Huang, Zhen
Zhang, Ye-fan
Cai, Jian-qiang
author_sort Wu, Xiao-long
collection PubMed
description BACKGROUND: Systemic inflammation (SI) is associated with tumor progression and overall survival (OS) in patients with hepatocellular carcinoma (HCC). The presence of some single nucleotide polymorphisms (SNPs) in the human leukocyte antigen (HLA) region can influence the prognosis of patients with hepatitis B virus (HBV)-related HCC, although the mechanism remains unknown. This study aimed to analyze the correlations between HLA gene polymorphisms and SI. PATIENTS AND METHODS: This study included 330 patients with HCC. The clinical parameters were reviewed, and five SNPs, namely rs2647073, rs3997872, rs3077, rs7453920, and rs7768538, were genotyped using the MassARRAY system. RESULTS: The rs3997872, rs7453920, and rs7768538 genotypes were found to be significantly associated with OS (P<0.05). The rs7453920 genotype was significantly associated with the neutrophil/lymphocyte ratio (NLR; P=0.001), which was used as an SI index with a threshold determined by receiver operating characteristic analysis. An elevated NLR was also an independent predictor of OS according to univariate and multivariate analyses (P<0.001). CONCLUSION: Our data show that HLA gene polymorphisms are associated with SI in patients with HBV-related HCC, and the absence of minor allele A (rs7453920) promotes SI and shortens OS.
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spelling pubmed-60747602018-08-13 Human leukocyte antigen gene polymorphisms are associated with systemic inflammation in hepatitis B virus-related hepatocellular carcinoma Wu, Xiao-long Li, Zhi-yu Bi, Xin-yu Zhao, Hong Zhao, Jian-jun Zhou, Jian-guo Han, Yue Huang, Zhen Zhang, Ye-fan Cai, Jian-qiang Cancer Manag Res Original Research BACKGROUND: Systemic inflammation (SI) is associated with tumor progression and overall survival (OS) in patients with hepatocellular carcinoma (HCC). The presence of some single nucleotide polymorphisms (SNPs) in the human leukocyte antigen (HLA) region can influence the prognosis of patients with hepatitis B virus (HBV)-related HCC, although the mechanism remains unknown. This study aimed to analyze the correlations between HLA gene polymorphisms and SI. PATIENTS AND METHODS: This study included 330 patients with HCC. The clinical parameters were reviewed, and five SNPs, namely rs2647073, rs3997872, rs3077, rs7453920, and rs7768538, were genotyped using the MassARRAY system. RESULTS: The rs3997872, rs7453920, and rs7768538 genotypes were found to be significantly associated with OS (P<0.05). The rs7453920 genotype was significantly associated with the neutrophil/lymphocyte ratio (NLR; P=0.001), which was used as an SI index with a threshold determined by receiver operating characteristic analysis. An elevated NLR was also an independent predictor of OS according to univariate and multivariate analyses (P<0.001). CONCLUSION: Our data show that HLA gene polymorphisms are associated with SI in patients with HBV-related HCC, and the absence of minor allele A (rs7453920) promotes SI and shortens OS. Dove Medical Press 2018-07-31 /pmc/articles/PMC6074760/ /pubmed/30104900 http://dx.doi.org/10.2147/CMAR.S167574 Text en © 2018 Wu et al. 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.
spellingShingle Original Research
Wu, Xiao-long
Li, Zhi-yu
Bi, Xin-yu
Zhao, Hong
Zhao, Jian-jun
Zhou, Jian-guo
Han, Yue
Huang, Zhen
Zhang, Ye-fan
Cai, Jian-qiang
Human leukocyte antigen gene polymorphisms are associated with systemic inflammation in hepatitis B virus-related hepatocellular carcinoma
title Human leukocyte antigen gene polymorphisms are associated with systemic inflammation in hepatitis B virus-related hepatocellular carcinoma
title_full Human leukocyte antigen gene polymorphisms are associated with systemic inflammation in hepatitis B virus-related hepatocellular carcinoma
title_fullStr Human leukocyte antigen gene polymorphisms are associated with systemic inflammation in hepatitis B virus-related hepatocellular carcinoma
title_full_unstemmed Human leukocyte antigen gene polymorphisms are associated with systemic inflammation in hepatitis B virus-related hepatocellular carcinoma
title_short Human leukocyte antigen gene polymorphisms are associated with systemic inflammation in hepatitis B virus-related hepatocellular carcinoma
title_sort human leukocyte antigen gene polymorphisms are associated with systemic inflammation in hepatitis b virus-related hepatocellular carcinoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074760/
https://www.ncbi.nlm.nih.gov/pubmed/30104900
http://dx.doi.org/10.2147/CMAR.S167574
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