Autoantibodies against glucose-regulated protein 78 as serological biomarkers in metastatic and recurrent hepatocellular carcinoma

• Published in: Oncotarget Vol. 8; no. 15; pp. 24828 - 24839
• Main Authors: Ying, Xia, Han, Su-Xia, He, Chen-Chen, Zhou, Cong-Ya, Dong, Yi-Ping, Cai, Meng-Jiao, Sui, Xin, Ma, Cheng-Xian, Sun, Xiao, Zhang, Yuan-Yuan, Gou, Wen-Li, Mason, Clifford, Zhu, Qing
• Format: Journal Article
• Language: English
• Published: United States Impact Journals LLC 11.04.2017
• Subjects: Autoantibodies - blood; Autoantibodies - immunology; Biomarkers, Tumor - blood; Biomarkers, Tumor - immunology; Carcinoma, Hepatocellular - blood; Carcinoma, Hepatocellular - immunology; Carcinoma, Hepatocellular - pathology; Case-Control Studies; Cell Line, Tumor; Enzyme-Linked Immunosorbent Assay; Fluorescent Antibody Technique, Indirect; HCT116 Cells; Heat-Shock Proteins - biosynthesis; Heat-Shock Proteins - immunology; HeLa Cells; Hep G2 Cells; Humans; Liver Neoplasms - blood; Liver Neoplasms - immunology; Liver Neoplasms - pathology; MCF-7 Cells; Neoplasm Metastasis; Research Paper; heptocellular carcinoma (HCC); proteomics; biomarker; autoantibodies; tumor associated antigens (TAA)
• ISSN: 1949-2553; 1949-2553
• DOI: 10.18632/oncotarget.15192

To identify Heptocellular carcinoma (HCC) associated antigens by proteomics, and validate whether autoantibodies against tumor-associated antigens (TAAs) could be used for diagnosis and conditional monitoring. The 78 kDa glucose regulated protein (GRP78) was selected as a candidate TAA. The titers of autoantibodies against 78 kDa glucose regulated protein (GRP78) from patients with HCC, liver cirrhosis (LC), and chronic hepatitis (CH) were significantly higher than that from normal controls (P<0.05, P<0.001, and P<0.01, respectively). The expression of autoantibodies against GRP78 was associated with clinical stage (P<0.01), portal vein invasion (P<0.05), and metastasis (P<0.05). The expression of anti-GRP78 antibodies was significantly higher 1 month after surgery in recurrent patients who had accepted hepatic resection 1 month after surgery compared to patients who had surgery before surgery or within 1 week after surgery (P<0.01 and P<0.001). Immunohistochemistry (IHC) showed higher expression of GRP78 in HCC compared to the non-HCC liver tissues (P <0.05). HCC serum with high titer of autoantibodies against TAAs were screened and used for a proteome-based approach to identify HCC associated antigens. Indirect enzyme-linked immunoassay (ELISA) was used to detect the corresponding autoantibodies against TAAs. GRP78 is an autoantigen that could stimulate autoimmune responses and serve as a potential marker for recurrent and metastatic progression in HCC.