Abstract. the global rising incidence of hepatocellular carcinoma (HCC), which parallels the increase of hepatitis C virus (HCV) prevalence, has sparked a renewed interest in discovering additional HCC serum markers. In this study, we investigated the clinical use of serum e-cadherin, ICAM, MMp-2, VeGF, OpN and β-catenin as potential diagnostic makers for HCV/genotype 4-associated HCC. twenty cases of healthy subjects, 11 cases with asymptomatic HCV/genotype 4 carriers (AsC), 28 chronic hepatitis (CH) cases and 32 patients with HCC were enrolled in this study. serum levels of proteins were measured by a sandwich-enzyme-linked (eLIsA) assay. the diagnostic accuracy of each candidate marker was evaluated using receiver-operating characteristic (rOC) curve analysis, reporting the area under the curve (AUC) and its 95% confidence interval (CI). We demonstrated that serum β-catenin levels were significantly elevated in patients with HCC compared to those with CH, AsC and healthy controls. Among the six studied markers, β-catenin was also found to be the only marker that can significantly discriminate between patients with HCC and those with CH; therefore, β-catenin could be considered as a potential marker for early diagnosis of HCV-associated HCC in patients infected with HCV genotype 4.
IntroductionHepatocellular carcinoma (HCC) is the fifth most common cancer and one of the leading causes of cancer death in the world (1). It has heterogeneous geographical distribution, with its greatest incidence in Asia and sub-saharan Africa, where hepatitis B infection is endemic (2). Its incidence has also been increasing steadily in the United states and Western europe due to the high prevalence of hepatitis C (3,4). egypt has the highest prevalence of hepatitis C virus (HCV) infection, with 14% of the population infected and seven million with chronic liver hepatitis (5,6). Little is known about the molecular mechanisms by which HCV initiates HCC. Molecular studies directed at mapping the etiology of HCV disease progression to HCC are expected to provide new insights on the management of this increasing problem and hence are of great global health interest. However, the lack of molecular makers that can characterize the stage of HCC, regardless of the etiologic factor, and tumor progression precludes the effective diagnosis and prognosis of HCC. Currently, HCC diagnosis relies on the radiology imaging systems, and elevated serum α-fetoprotein (AFp). serum AFp is not always elevated to a diagnostic level in all patients in small HCC, thus, considerable numbers of patients with more advanced stages would be missed unless other diagnostic tools are used (7,8). Moreover, the level of AFp may be elevated in non-malignant chronic liver diseases, including chronic hepatitis and cirrhosis (9,10). several biomarkers, such as des-γ-carboxyprothrombin/prothrombin induced by vitamin K absence-II, lens cularis agglutininreactive (AFp-L3), and glypican-3, have been examined for their ability to diagnose early HCC (11). However, there is a...