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Identification of the Level of Exosomal Protein by Parallel Reaction Monitoring Technology in HCC Patients
PURPOSE: Reliable biomarkers for the diagnosis and differential diagnosis of various stages of liver cancer are lacking. In this study, we aim to detect the levels of differentially expressed proteins (DEPs) in serum exosomes of patients with different liver diseases using a sensitive method. PATIEN...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578473/ https://www.ncbi.nlm.nih.gov/pubmed/36267426 http://dx.doi.org/10.2147/IJGM.S384140 |
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author | Huang, Hui Zhang, Qiqi Zhang, Yong Sun, Xueying Liu, Chunyan Wang, Qi Huang, Yushuang Li, Qingwei Wu, Zepan Pu, Chunwen Sun, Aijun |
author_facet | Huang, Hui Zhang, Qiqi Zhang, Yong Sun, Xueying Liu, Chunyan Wang, Qi Huang, Yushuang Li, Qingwei Wu, Zepan Pu, Chunwen Sun, Aijun |
author_sort | Huang, Hui |
collection | PubMed |
description | PURPOSE: Reliable biomarkers for the diagnosis and differential diagnosis of various stages of liver cancer are lacking. In this study, we aim to detect the levels of differentially expressed proteins (DEPs) in serum exosomes of patients with different liver diseases using a sensitive method. PATIENTS AND METHODS: Exosomes were purified and validated. The expression of DEPs in exosomes from patients with chronic hepatitis B (CHB), liver cirrhosis (LC) and hepatocellular carcinoma (HCC) was validated by parallel reaction monitoring (PRM) technology and Western blotting, and the biological functions were analyzed by bioinformatics analysis. RESULTS: A total of 11 DEPs were identified by PRM technology. Significantly higher level of haptoglobin (Hp) was detected in HCC patients as compared to LC and CHB patients. HCC patients had a significantly lower level of transthyretin (TTR) in the patients with CHB. Among the patients with HCC who undertaken surgery, the postoperative levels of CRP, SERPINA3 and Heparin cofactor 2 (SERPIND1) were significantly reduced compared to their respective preoperative levels. CONCLUSION: Hp and TTR may be potential markers for early diagnosis of HCC. CRP, SERPINA3 and SERPIND1 may serve as potential prognostic indicators for HCC patients undertaken surgery. |
format | Online Article Text |
id | pubmed-9578473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-95784732022-10-19 Identification of the Level of Exosomal Protein by Parallel Reaction Monitoring Technology in HCC Patients Huang, Hui Zhang, Qiqi Zhang, Yong Sun, Xueying Liu, Chunyan Wang, Qi Huang, Yushuang Li, Qingwei Wu, Zepan Pu, Chunwen Sun, Aijun Int J Gen Med Original Research PURPOSE: Reliable biomarkers for the diagnosis and differential diagnosis of various stages of liver cancer are lacking. In this study, we aim to detect the levels of differentially expressed proteins (DEPs) in serum exosomes of patients with different liver diseases using a sensitive method. PATIENTS AND METHODS: Exosomes were purified and validated. The expression of DEPs in exosomes from patients with chronic hepatitis B (CHB), liver cirrhosis (LC) and hepatocellular carcinoma (HCC) was validated by parallel reaction monitoring (PRM) technology and Western blotting, and the biological functions were analyzed by bioinformatics analysis. RESULTS: A total of 11 DEPs were identified by PRM technology. Significantly higher level of haptoglobin (Hp) was detected in HCC patients as compared to LC and CHB patients. HCC patients had a significantly lower level of transthyretin (TTR) in the patients with CHB. Among the patients with HCC who undertaken surgery, the postoperative levels of CRP, SERPINA3 and Heparin cofactor 2 (SERPIND1) were significantly reduced compared to their respective preoperative levels. CONCLUSION: Hp and TTR may be potential markers for early diagnosis of HCC. CRP, SERPINA3 and SERPIND1 may serve as potential prognostic indicators for HCC patients undertaken surgery. Dove 2022-10-14 /pmc/articles/PMC9578473/ /pubmed/36267426 http://dx.doi.org/10.2147/IJGM.S384140 Text en © 2022 Huang et al. https://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/ (https://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 Huang, Hui Zhang, Qiqi Zhang, Yong Sun, Xueying Liu, Chunyan Wang, Qi Huang, Yushuang Li, Qingwei Wu, Zepan Pu, Chunwen Sun, Aijun Identification of the Level of Exosomal Protein by Parallel Reaction Monitoring Technology in HCC Patients |
title | Identification of the Level of Exosomal Protein by Parallel Reaction Monitoring Technology in HCC Patients |
title_full | Identification of the Level of Exosomal Protein by Parallel Reaction Monitoring Technology in HCC Patients |
title_fullStr | Identification of the Level of Exosomal Protein by Parallel Reaction Monitoring Technology in HCC Patients |
title_full_unstemmed | Identification of the Level of Exosomal Protein by Parallel Reaction Monitoring Technology in HCC Patients |
title_short | Identification of the Level of Exosomal Protein by Parallel Reaction Monitoring Technology in HCC Patients |
title_sort | identification of the level of exosomal protein by parallel reaction monitoring technology in hcc patients |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578473/ https://www.ncbi.nlm.nih.gov/pubmed/36267426 http://dx.doi.org/10.2147/IJGM.S384140 |
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