MS Proteomics Research Group, Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117, Budapest, Hungary.
Department of Inorganic and Analytical Chemistry, Budapest University of Technology and Economics, Szent Gellért tér 4, 1111, Budapest, Hungary.
Anal Bioanal Chem. 2022 May;414(13):3837-3846. doi: 10.1007/s00216-022-04025-3. Epub 2022 Mar 28.
Chronic liver diseases have both high incidence and mortality rates; therefore, a deeper understanding of the underlying molecular mechanisms is essential. We have determined the content and sulfation pattern of chondroitin sulfate (CS) and heparan sulfate (HS) in human hepatocellular carcinoma and cirrhotic liver tissues, considering the etiology of the diseases. A variety of pathological conditions such as alcoholic liver disease, hepatitis B and C virus infections, and primary sclerosing cholangitis were studied. Major differences were observed in the total abundance and sulfation pattern of CS and HS chains. For example, the 6-O-sulfation of CS is fundamentally different regarding etiologies of cirrhosis, and a 2-threefold increase in HS N-sulfation/O-sulfation ratio was observed in hepatocellular carcinoma compared to cirrhotic tissues.
慢性肝脏疾病具有高发病率和死亡率;因此,深入了解其潜在的分子机制至关重要。我们已经确定了人类肝癌和肝硬化组织中软骨素硫酸酯 (CS) 和肝素硫酸酯 (HS) 的含量和硫酸化模式,考虑到疾病的病因。研究了多种病理情况,如酒精性肝病、乙型和丙型肝炎病毒感染以及原发性硬化性胆管炎。CS 和 HS 链的总丰度和硫酸化模式存在显著差异。例如,肝硬化的 CS 6-O 硫酸化在病因上存在根本差异,与肝硬化组织相比,肝癌中 HS N-硫酸化/ O-硫酸化比值增加了 2-3 倍。