Abstract | OBJECTIVE: PATIENTS AND METHODS: We retrospectively analyzed the data of patients who were treated in our hospitals. iTRAQ coupled with mass spectrometry was used to identify candidate serum proteins in a discovery set (n = 36) including AFP-negative HCC and LC patients. After Western blot detection, potential serum biomarkers were confirmed using ELISA in a validation set (n = 90). The diagnostic performance of the selected proteins was assessed using receiver operating characteristic (ROC). RESULTS: PON1 and ATIII were selected as target proteins and were significantly higher in LC than those in AFP-negative HCC patients as validated by Western blot and ELISA, which was consistent with the result of iTRAQ. The AUC was 0.848 as PON1 and ATIII were combined (sensitivity: 80.0%; specificity: 73.3%), and performed much better than that of a single biomarker. CONCLUSION: These findings suggest that PON1 and ATIII have the potential to serve as effective biomarkers for distinguishing AFP-negative HCC from cirrhosis.
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Authors | Xinyi Cao, Zhao Cao, Chao Ou, Lei Zhang, Yanhua Chen, Yanqiu Li, Bo Zhu, Hong Shu |
Journal | Clinics and research in hepatology and gastroenterology
(Clin Res Hepatol Gastroenterol)
Vol. 45
Issue 5
Pg. 101583
(09 2021)
ISSN: 2210-741X [Electronic] France |
PMID | 33756265
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2020 Elsevier Masson SAS. All rights reserved. |
Chemical References |
- Antithrombins
- Biomarkers
- alpha-Fetoproteins
- Aryldialkylphosphatase
|
Topics |
- Antithrombins
(blood)
- Aryldialkylphosphatase
(blood)
- Biomarkers
(blood)
- Carcinoma, Hepatocellular
(blood, diagnosis)
- Humans
- Liver Cirrhosis
(blood, diagnosis)
- Liver Neoplasms
(blood, diagnosis)
- Retrospective Studies
- alpha-Fetoproteins
(metabolism)
|