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Hepatitis B Virus Core Promoter Double Mutations (A1762T, G1764A) Are Associated with Lower Levels of Serum Dihydrolipoyl Dehydrogenase

OBJECTIVES: The aim of this study was to identify serum proteins with differential concentrations between hepatocellular carcinoma (HCC) patients and HBsAg asymptomatic carriers among individuals infected with hepatitis B virus (HBV) with basal core promoter (BCP) double mutations (A1762T, G1764A)....

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Autores principales: Jiang, Zhi-Hua, Chen, Qin-Yan, Harrison, Tim J., Li, Guo-Jian, Wang, Xue-Yan, Li, Hai, Hu, Li-Ping, Li, Kai-Wen, Yang, Qing-Li, Tan, Chao, Fang, Zhong-Liao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5079069/
https://www.ncbi.nlm.nih.gov/pubmed/27303803
http://dx.doi.org/10.1159/000445319
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author Jiang, Zhi-Hua
Chen, Qin-Yan
Harrison, Tim J.
Li, Guo-Jian
Wang, Xue-Yan
Li, Hai
Hu, Li-Ping
Li, Kai-Wen
Yang, Qing-Li
Tan, Chao
Fang, Zhong-Liao
author_facet Jiang, Zhi-Hua
Chen, Qin-Yan
Harrison, Tim J.
Li, Guo-Jian
Wang, Xue-Yan
Li, Hai
Hu, Li-Ping
Li, Kai-Wen
Yang, Qing-Li
Tan, Chao
Fang, Zhong-Liao
author_sort Jiang, Zhi-Hua
collection PubMed
description OBJECTIVES: The aim of this study was to identify serum proteins with differential concentrations between hepatocellular carcinoma (HCC) patients and HBsAg asymptomatic carriers among individuals infected with hepatitis B virus (HBV) with basal core promoter (BCP) double mutations (A1762T, G1764A). METHODS: iTRAQ and liquid chromatography-tandem mass spectrometry were used to identify differentially expressed protein, and an ELISA test was used for the validation test. RESULTS: The total number of proteins identified was 1,125, of which 239 showed statistically significant differences in their expression. The relative concentrations of serum dihydrolipoyl dehydrogenase (DLD), which showed the most significant correlation with liver diseases and infection, were significantly lower in HCC patients than asymptomatic HBsAg carriers and individuals negative for HBsAg. However, only the difference between HCC patients with BCP double mutations and HBsAg-negative individuals could be confirmed by ELISA. Meanwhile, we found that the concentrations of serum DLD in those infected with HBV with BCP double mutations were significantly lower than in individuals with the wild-type BCP. However, the difference in the concentrations of serum DLD between individuals with wild-type BCP and those negative for HBsAg was not significant. CONCLUSIONS: HBV with BCP double mutations are associated with lower concentrations of serum DLD.
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spelling pubmed-50790692016-10-27 Hepatitis B Virus Core Promoter Double Mutations (A1762T, G1764A) Are Associated with Lower Levels of Serum Dihydrolipoyl Dehydrogenase Jiang, Zhi-Hua Chen, Qin-Yan Harrison, Tim J. Li, Guo-Jian Wang, Xue-Yan Li, Hai Hu, Li-Ping Li, Kai-Wen Yang, Qing-Li Tan, Chao Fang, Zhong-Liao Intervirology Original Paper OBJECTIVES: The aim of this study was to identify serum proteins with differential concentrations between hepatocellular carcinoma (HCC) patients and HBsAg asymptomatic carriers among individuals infected with hepatitis B virus (HBV) with basal core promoter (BCP) double mutations (A1762T, G1764A). METHODS: iTRAQ and liquid chromatography-tandem mass spectrometry were used to identify differentially expressed protein, and an ELISA test was used for the validation test. RESULTS: The total number of proteins identified was 1,125, of which 239 showed statistically significant differences in their expression. The relative concentrations of serum dihydrolipoyl dehydrogenase (DLD), which showed the most significant correlation with liver diseases and infection, were significantly lower in HCC patients than asymptomatic HBsAg carriers and individuals negative for HBsAg. However, only the difference between HCC patients with BCP double mutations and HBsAg-negative individuals could be confirmed by ELISA. Meanwhile, we found that the concentrations of serum DLD in those infected with HBV with BCP double mutations were significantly lower than in individuals with the wild-type BCP. However, the difference in the concentrations of serum DLD between individuals with wild-type BCP and those negative for HBsAg was not significant. CONCLUSIONS: HBV with BCP double mutations are associated with lower concentrations of serum DLD. S. Karger AG 2016-09 2016-06-16 /pmc/articles/PMC5079069/ /pubmed/27303803 http://dx.doi.org/10.1159/000445319 Text en Copyright © 2016 by S. Karger AG, Basel http://creativecommons.org/licenses/by/4.0/ This article is licensed under the Creative Commons Attribution 4.0 International License (CC BY) (http://www.karger.com/Services/OpenAccessLicense). Usage, derivative works and distribution are permitted provided that proper credit is given to the author and the original publisher.
spellingShingle Original Paper
Jiang, Zhi-Hua
Chen, Qin-Yan
Harrison, Tim J.
Li, Guo-Jian
Wang, Xue-Yan
Li, Hai
Hu, Li-Ping
Li, Kai-Wen
Yang, Qing-Li
Tan, Chao
Fang, Zhong-Liao
Hepatitis B Virus Core Promoter Double Mutations (A1762T, G1764A) Are Associated with Lower Levels of Serum Dihydrolipoyl Dehydrogenase
title Hepatitis B Virus Core Promoter Double Mutations (A1762T, G1764A) Are Associated with Lower Levels of Serum Dihydrolipoyl Dehydrogenase
title_full Hepatitis B Virus Core Promoter Double Mutations (A1762T, G1764A) Are Associated with Lower Levels of Serum Dihydrolipoyl Dehydrogenase
title_fullStr Hepatitis B Virus Core Promoter Double Mutations (A1762T, G1764A) Are Associated with Lower Levels of Serum Dihydrolipoyl Dehydrogenase
title_full_unstemmed Hepatitis B Virus Core Promoter Double Mutations (A1762T, G1764A) Are Associated with Lower Levels of Serum Dihydrolipoyl Dehydrogenase
title_short Hepatitis B Virus Core Promoter Double Mutations (A1762T, G1764A) Are Associated with Lower Levels of Serum Dihydrolipoyl Dehydrogenase
title_sort hepatitis b virus core promoter double mutations (a1762t, g1764a) are associated with lower levels of serum dihydrolipoyl dehydrogenase
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5079069/
https://www.ncbi.nlm.nih.gov/pubmed/27303803
http://dx.doi.org/10.1159/000445319
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