We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

LabMedica

Download Mobile App
Recent News Expo Medica 2024 Clinical Chem. Molecular Diagnostics Hematology Immunology Microbiology Pathology Technology Industry Focus

Altered Glycosylation Associated with Dedifferentiation of Hepatocellular Carcinoma

By LabMedica International staff writers
Posted on 16 Mar 2020
Hepatocellular carcinoma (HCC) is a common cancer with poor prognosis. Liver cancer is the sixth most common type of cancer worldwide, and the fourth most common cause of cancer death. HCC accounts for most primary liver cancers.

Glycosylation is involved in many essential biological processes such as cell differentiation, proliferation, and adhesion; immune response; and receptor activation. However, aberrant glycosylation results in many dysfunctions and diseases. Lectin microarray is a method capable of analyzing glycan profiles comprehensively and sensitively with 45 lectins utilizing lectin specificity to detect specific structures of glycans.

Image: GlycoStation Reader 1200 is an ultra-high speed and highly sensitive optical microarray scanner utilizing the principle of evanescent-field fluorescence excitation to scan an entire microarray slide in only two minutes (Photo courtesy of GlycoTechnica Ltd).
Image: GlycoStation Reader 1200 is an ultra-high speed and highly sensitive optical microarray scanner utilizing the principle of evanescent-field fluorescence excitation to scan an entire microarray slide in only two minutes (Photo courtesy of GlycoTechnica Ltd).

Gastroenterologists at the Oita University Faculty of Medicine (Oita, Japan) analyzed resected 50 HCC specimens using lectin microarray to comprehensively and sensitively analyze glycan profiles. The samples were prepared for laser microdissection by fixing in formalin, embedding in paraffin, then sectioning at a thickness of 5 μm. Lectin microarray was performed and performed immunohistochemical staining of mannosyl(α-1,3-)-glycoprotein β-1,2-N-acetylglucosaminyltransferase (MGAT1), which is an essential glycosyltransferase that converts high-mannose glycans to complex- or hybrid-type N-glycans. Fluorescent images were obtained with the GlycoStation Reader 1200 (GlycoTechnica Ltd, Yokohama, Japan) using the evanescent-wave excitation method.

The scientists reported that four lectins from Narcissus pseudonarcissus agglutinin (NPA), Concanavalin A, Galanthus nivalis agglutinin, and Calystegia sepium agglutinin were significantly elevated in moderately-differentiated components of HCC compared with well-differentiated components, and all lectins showed binding specificity to high-mannose glycans. All the lectins showed specificity to high-mannose glycan structures and none were significantly decreased by dedifferentiation. Immunohistochemical staining revealed significantly increased NPA expression and decreased MGAT1 expression in moderately-differentiated components. Low MGAT1 expression in moderately-differentiated components of tumors was associated with intrahepatic metastasis and had tendency for poor prognosis.

The authors concluded that dedifferentiation of well-differentiated HCC is associated with increased high-mannose glycans. Furthermore, MGAT1 may play a role in HCC dedifferentiation. The study was published on March 6, 2020 in the journal BMC Cancer.

Related Links:
Oita University Faculty of Medicine
GlycoTechnica Ltd



Gold Member
Hematology Analyzer
Swelab Lumi
Automated Blood Typing System
IH-500 NEXT
New
Free Human Prostate-Specific Antigen CLIA
LIAISON fPSA
New
Malaria Rapid Test
OnSite Malaria Pf/Pan Ag Rapid Test

Latest Clinical Chem. News

POC Saliva Testing Device Predicts Heart Failure in 15 Minutes

Screening Tool Detects Multiple Health Conditions from Single Blood Drop

Integrated Chemistry and Immunoassay Analyzer with Extensive Assay Menu Offers Flexibility, Scalability and Data Commutability