Biochemical Research Methods Biochemistry & Molecular Biology Life Sciences & Biomedicine Science & Technology
PurposeHepatocellular carcinoma (HCC) is a primary cancer of the liver that is predominantly the result of infection with a hepatotropic virus such as hepatitis B virus or hepatitis C virus. As liver cancer is often asymptomatic, the development of sensitive noninvasive biomarkers is needed for early detection and improved survival.
Experimental designWe have previously identified alterations in the N-linked glycosylation of serum proteins with the development of HCC and identified many of the proteins that contained the altered glycosylation. In the current study, we compared the ability of the identified proteins to diagnose HCC with the total serum glycan analysis.
ResultsSurprisingly, glycan analysis of total serum had the greatest ability to distinguish HCC from cirrhosis with an AUROC of 0.851, a sensitivity of 73% at a specificity of 88%. When total glycan sequencing was combined with alpha-fetoprotein (AFP), the sensitivity increased to 95% at a specificity of 90%.
Conclusion and clinical relevanceChanges in glycosylation as detected in whole serum could be used to diagnose HCC with greater sensitivity and specificity than that observed through the analysis of specific protein glycoforms or protein levels. Such an assay could have value in the management of those at risk for the development of HCC.
Total serum glycan analysis is superior to lectin-FLISA for the early detection of hepatocellular carcinoma
Creators
Mary Ann Comunale - Drexel University
Mengjun Wang - Drexel University
Nikhil Anbarasan - Hepatitis B Foundation
Lucy Betesh - Drexel University
Aykan Karabudak - Hepatitis B Foundation
Ethan Moritz - Hepatitis B Foundation
Karthik Devarajan - Fox Chase Cancer Center
Jorge Marrero - University of Michigan–Ann Arbor
Timothy M. Block - Drexel University
Anand Mehta - Drexel University
Publication Details
Proteomics. Clinical applications, v 7(9-10), pp 690-700
Publisher
Wiley
Number of pages
11
Grant note
R01 CA120206; U01 CA168856 / National Cancer Institute (NCI); United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Cancer Institute (NCI)
Hepatitis B Foundation
R01CA120206 / NATIONAL CANCER INSTITUTE; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Cancer Institute (NCI)
Resource Type
Journal article
Language
English
Academic Unit
Microbiology and Immunology
Web of Science ID
WOS:000325479300011
Scopus ID
2-s2.0-84885938288
Other Identifier
991019168703404721
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