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Alpha-1 antitrypsin is a potential biomarker for hepatitis B
BACKGROUND: Function exertion of specific proteins are key factors in disease progression, thus the systematical identification of those specific proteins is a prerequisite to understand various diseases. Though many proteins have been verified to impact on hepatitis, no systematical protein screeni...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120791/ https://www.ncbi.nlm.nih.gov/pubmed/21639939 http://dx.doi.org/10.1186/1743-422X-8-274 |
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author | Tan, Xu-fei Wu, Shan-shan Li, Shu-ping Chen, Zhi Chen, Feng |
author_facet | Tan, Xu-fei Wu, Shan-shan Li, Shu-ping Chen, Zhi Chen, Feng |
author_sort | Tan, Xu-fei |
collection | PubMed |
description | BACKGROUND: Function exertion of specific proteins are key factors in disease progression, thus the systematical identification of those specific proteins is a prerequisite to understand various diseases. Though many proteins have been verified to impact on hepatitis, no systematical protein screening has been documented to hepatitis B virus (HBV) induced hepatitis, hindering the comprehensive understanding to this severe disease. AIM: To identify the major proteins in the progression of HBV infection from mild stage to severe stage. METHODS: We performed an integrated strategy by combining two-dimensional electrophoresis (2-DE), peptide mass fingerprinting (PMF) analysis, and tissue microarray techniques to screen the functional proteins and detect the localization of those proteins. RESULTS: Interestingly, MS/MS identification revealed the expression level of alpha-1 antitrypsin (AAT) was significantly elevated in serum samples from patients with severe chronic hepatitis. Immunoblotting with a specific AAT antibody confirmed that AAT is highly expressed in serum samples from patients with hepatic carcinoma and severe chronic hepatitis. Furthermore, we observed that AAT is with highest expression in normal tissue and cells, but lowest in hepatic carcinoma and severe chronic hepatitis tissues and cells, suggesting the specific secretion of AAT from tissues and cells to serum. CONCLUSION: These results suggest the possibility of AAT as a potential biomarker for hepatitis B in diagnosis. |
format | Online Article Text |
id | pubmed-3120791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31207912011-06-23 Alpha-1 antitrypsin is a potential biomarker for hepatitis B Tan, Xu-fei Wu, Shan-shan Li, Shu-ping Chen, Zhi Chen, Feng Virol J Research BACKGROUND: Function exertion of specific proteins are key factors in disease progression, thus the systematical identification of those specific proteins is a prerequisite to understand various diseases. Though many proteins have been verified to impact on hepatitis, no systematical protein screening has been documented to hepatitis B virus (HBV) induced hepatitis, hindering the comprehensive understanding to this severe disease. AIM: To identify the major proteins in the progression of HBV infection from mild stage to severe stage. METHODS: We performed an integrated strategy by combining two-dimensional electrophoresis (2-DE), peptide mass fingerprinting (PMF) analysis, and tissue microarray techniques to screen the functional proteins and detect the localization of those proteins. RESULTS: Interestingly, MS/MS identification revealed the expression level of alpha-1 antitrypsin (AAT) was significantly elevated in serum samples from patients with severe chronic hepatitis. Immunoblotting with a specific AAT antibody confirmed that AAT is highly expressed in serum samples from patients with hepatic carcinoma and severe chronic hepatitis. Furthermore, we observed that AAT is with highest expression in normal tissue and cells, but lowest in hepatic carcinoma and severe chronic hepatitis tissues and cells, suggesting the specific secretion of AAT from tissues and cells to serum. CONCLUSION: These results suggest the possibility of AAT as a potential biomarker for hepatitis B in diagnosis. BioMed Central 2011-06-05 /pmc/articles/PMC3120791/ /pubmed/21639939 http://dx.doi.org/10.1186/1743-422X-8-274 Text en Copyright ©2011 Tan et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Tan, Xu-fei Wu, Shan-shan Li, Shu-ping Chen, Zhi Chen, Feng Alpha-1 antitrypsin is a potential biomarker for hepatitis B |
title | Alpha-1 antitrypsin is a potential biomarker for hepatitis B |
title_full | Alpha-1 antitrypsin is a potential biomarker for hepatitis B |
title_fullStr | Alpha-1 antitrypsin is a potential biomarker for hepatitis B |
title_full_unstemmed | Alpha-1 antitrypsin is a potential biomarker for hepatitis B |
title_short | Alpha-1 antitrypsin is a potential biomarker for hepatitis B |
title_sort | alpha-1 antitrypsin is a potential biomarker for hepatitis b |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120791/ https://www.ncbi.nlm.nih.gov/pubmed/21639939 http://dx.doi.org/10.1186/1743-422X-8-274 |
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