Compositional Analysis of Glycosaminoglycans in Different Lung Cancer Types—A Pilot Study

Author:

Pál Domonkos12ORCID,Tóth Gábor1ORCID,Sugár Simon12ORCID,Fügedi Kata Dorina13,Szabó Dániel1ORCID,Kovalszky Ilona4ORCID,Papp Dávid56,Schlosser Gitta5ORCID,Tóth Csaba7,Tornóczky Tamás8,Drahos László1ORCID,Turiák Lilla1ORCID

Affiliation:

1. MS Proteomics Research Group, Research Centre for Natural Sciences, H-1117 Budapest, Hungary

2. Doctoral School of Pharmaceutical Sciences, Semmelweis University, H-1085 Budapest, Hungary

3. Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, H-1111 Budapest, Hungary

4. 1st Department of Pathology and Experimental Cancer Research, Semmelweis University, H-1085 Budapest, Hungary

5. MTA-ELTE Lendület Ion Mobility Mass Spectrometry Research Group, ELTE Eötvös Loránd University, H-1117 Budapest, Hungary

6. Hevesy György PhD School of Chemistry, ELTE Eötvös Loránd University, H-1117 Budapest, Hungary

7. Teaching Hospital Markusovszky, University of Pécs, H-9700 Szombathely, Hungary

8. Department of Pathology, Faculty of Medicine and Clinical Center, University of Pécs, H-7624 Pécs, Hungary

Abstract

Lung cancer is one of the most commonly diagnosed cancer types. Studying the molecular changes that occur in lung cancer is important to understand tumor formation and identify new therapeutic targets and early markers of the disease to decrease mortality. Glycosaminoglycan chains play important roles in various signaling events in the tumor microenvironment. Therefore, we have determined the quantity and sulfation characteristics of chondroitin sulfate and heparan sulfate in formalin-fixed paraffin-embedded human lung tissue samples belonging to different lung cancer types as well as tumor adjacent normal areas. Glycosaminoglycan disaccharide analysis was performed using HPLC-MS following on-surface lyase digestion. Significant changes were identified predominantly in the case of chondroitin sulfate; for example, the total amount was higher in tumor tissue compared to the adjacent normal tissue. We also observed differences in the degree of sulfation and relative proportions of individual chondroitin sulfate disaccharides between lung cancer types and adjacent normal tissue. Furthermore, the differences in the 6-O-/4-O-sulfation ratio of chondroitin sulfate were different between the lung cancer types. Our pilot study revealed that further investigation of the role of chondroitin sulfate chains and enzymes involved in their biosynthesis is an important aspect of lung cancer research.

Funder

National Research, Development, and Innovation Fund of Hungary

Hungarian Academy of Sciences

Hungarian Ministry for Innovation and Technology

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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