| Literature DB >> 26457017 |
Nobuhiro Tsuchiya1, Yu Sawada1, Itaru Endo1, Keigo Saito1, Yasushi Uemura1, Tetsuya Nakatsura1.
Abstract
Hepatocellular carcinoma (HCC) is the fifth most common cancer and the second leading cause of cancer-related deaths worldwide. Although the prognosis of patients with HCC is generally poor, the 5-year survival rate is > 70% if patients are diagnosed at an early stage. However, early diagnosis of HCC is complicated by the coexistence of inflammation and cirrhosis. Thus, novel biomarkers for the early diagnosis of HCC are required. Currently, the diagnosis of HCC without pathological correlation is achieved by analyzing serum α-fetoprotein levels combined with imaging techniques. Advances in genomics and proteomics platforms and biomarker assay techniques over the last decade have resulted in the identification of numerous novel biomarkers and have improved the diagnosis of HCC. The most promising biomarkers, such as glypican-3, osteopontin, Golgi protein-73 and nucleic acids including microRNAs, are most likely to become clinically validated in the near future. These biomarkers are not only useful for early diagnosis of HCC, but also provide insight into the mechanisms driving oncogenesis. In addition, such molecular insight creates the basis for the development of potentially more effective treatment strategies. In this article, we provide an overview of the biomarkers that are currently used for the early diagnosis of HCC.Entities:
Keywords: Biomarker; Des-γ-carboxyprothrombin; Glypican-3; Golgi protein-73; Hepatocellular carcinoma; MicroRNAs; Osteopontin; Squamous cell carcinoma antigen; α-fetoprotein; α-fetoprotein-L3
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Year: 2015 PMID: 26457017 PMCID: PMC4588079 DOI: 10.3748/wjg.v21.i37.10573
Source DB: PubMed Journal: World J Gastroenterol ISSN: 1007-9327 Impact factor: 5.742