Premium
Identification of complement C3a as a candidate biomarker in human chronic hepatitis C and HCV‐related hepatocellular carcinoma using a proteomics approach
Author(s) -
Lee INeng,
Chen ChienHung,
Sheu JinChuan,
Lee HsuanShu,
Huang GuanTarn,
Chen DingShinn,
Yu ChenYin,
Wen ChuLing,
Lu FungJou,
Chow LuPing
Publication year - 2006
Publication title -
proteomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.26
H-Index - 167
eISSN - 1615-9861
pISSN - 1615-9853
DOI - 10.1002/pmic.200500488
Subject(s) - hepatocellular carcinoma , biomarker , medicine , hepatitis c virus , hepatitis c , proteomics , immunoassay , liver cancer , immunology , virus , biology , antibody , gene , biochemistry
Abstract Although the significant risk factors for hepatocellular carcinoma (HCC) are well known from epidemiological studies, diagnosis of this disease at an early stage is difficult, and HCC remains one of the leading causes of cancer death worldwide. Thus, to identify any useful HCC‐related biomarkers is still a need. We performed SELDI‐TOF MS to identify differentially expressed proteins in HCC serum using weak cation exchange protein chips. Protein characterization was performed by 2‐DE separation and nano flow LC‐MS/MS. A total of 55 sera were collected from HCC patients and compared with those from 48 patients with chronic hepatitis and 9 healthy individuals. A candidate marker of about 8900 Da was detected as differentially expressed in patients with chronic hepatitis C and hepatitis C virus (HCV)‐related HCC. We identified this differentially expressed protein as complement C3a. The expression of C3a in HCC sera was further validated by PS20 chip immunoassay and Western blotting. Complement C3a was found to be elevated in patients with chronic hepatitis C and HCV‐related HCC. The combination of SELDI‐TOF MS and 2‐DE provides a solution to identify disease‐associated serum biomarkers.