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A Quantitative Proteomic Approach for Identification of Potential Biomarkers in Hepatocellular Carcinoma

Published on Oct 3, 2008in Journal of Proteome Research3.78
· DOI :10.1021/pr800197z
Raghothama Chaerkady33
Estimated H-index: 33
,
H. C. Harsha5
Estimated H-index: 5
(Johns Hopkins University)
+ 10 AuthorsPaul J. Thuluvath31
Estimated H-index: 31
(Johns Hopkins University)
Abstract
Hepatocellular carcinoma (HCC) is the fifth most common cancer worldwide. In this study, our objective was to identify differentially regulated proteins in HCC through a quantitative proteomic approach using iTRAQ. More than 600 proteins were quantitated of which 59 proteins were overexpressed and 92 proteins were underexpressed in HCC as compared to adjacent normal tissue. Several differentially expressed proteins were not implicated previously in HCC. A subset of these proteins (six each from upregulated and downregulated groups) was further validated using immunoblotting and immunohistochemical labeling. Some of the overexpressed proteins with no previous description in the context of HCC include fibroleukin, interferon induced 56 kDa protein, milk fat globule-EGF factor 8, and myeloidassociated differentiation marker. Interestingly, all the enzymes of urea metabolic pathway were dramatically downregulated. Immunohistochemical labeling confirmed differential expression of fibroleukin, myeloid associated differentiation marker and ornithine carbamoyl transferase in majority of HCC samples analyzed. Our results demonstrate quantitative proteomics as a robust discovery tool for the identification of differentially regulated proteins in cancers.
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