Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/119042
Author(s): Mereiter, S
Magalhães, A
Adamczyk, B.
Jin, C
Almeida, A
Drici, L
Ibáñez-Vea, M
Gomes, C
Ferreira, JA
Afonso, L
Santos, L
Larsen, M
Kolarich, D
Karlsson, N
Reis, CA
Title: Glycomic analysis of gastric carcinoma cells discloses glycans as modulators of RON receptor tyrosine kinase activation in cancer
Publisher: Elsevier
Issue Date: 2016
Abstract: Background Terminal a2-3 and a2-6 sialylation of glycans precludes further chain elongation, leading to the biosynthesis of cancer relevant epitopes such as sialyl-Lewis X (SLe X ). SLe X overexpression is associated with tumor aggressive phenotype and patients' poor prognosis. Methods MKN45 gastric carcinoma cells transfected with the sialyltransferase ST3GAL4 were established as a model overexpressing sialylated terminal glycans. We have evaluated at the structural level the glycome and the sialoproteome of this gastric cancer cell line applying liquid chromatography and mass spectrometry. We further validated an identified target expression by proximity ligation assay in gastric tumors. Results Our results showed that ST3GAL4 overexpression leads to several glycosylation alterations, including reduced O-glycan extension and decreased bisected and increased branched N-glycans. A shift from a2-6 towards a2-3 linked sialylated N-glycans was also observed. Sialoproteomic analysis further identified 47 proteins with significantly increased sialylated N-glycans. These included integrins, insulin receptor, carcinoembryonic antigens and RON receptor tyrosine kinase, which are proteins known to be key players in malignancy. Further analysis of RON confirmed its modification with SLe X and the concomitant activation. SLe X and RON co-expression was validated in gastric tumors. Conclusion The overexpression of ST3GAL4 interferes with the overall glycophenotype of cancer cells affecting a multitude of key proteins involved in malignancy. Aberrant glycosylation of the RON receptor was shown as an alternative mechanism of oncogenic activation. General significance This study provides novel targets and points to an integrative tumor glycomic/proteomic-profiling for gastric cancer patients' stratification. This article is part of a Special Issue entitled "Glycans in personalised medicine" Guest Editor: Professor Gordan Lauc.
Subject: Gene Expression Regulation, Enzymologic
Gene Expression Regulation, Neoplastic
Glycomics
Humans
Lewis X Antigen/biosynthesis
Lewis X Antigen/genetics
Neoplasm Proteins/biosynthesis
Neoplasm Proteins/genetics
Polysaccharides/biosynthesis
Polysaccharides/genetics
Receptor Protein-Tyrosine Kinases/genetics
Receptor Protein-Tyrosine Kinases/metabolism
Sialyltransferases/biosynthesis
Sialyltransferases/genetics
Stomach
Neoplasms/genetics
Stomach Neoplasms/metabolism
URI: https://hdl.handle.net/10216/119042
Source: Biochimica et Biophysica Acta - General Subjects, vol.1860(8), p. 1795-1808
Related Information: info:eu-repo/grantAgreement/FCT/COMPETE/132983/PT
info:eu-repo/grantAgreement/FCT/COMPETE/125428/PT
info:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBPD%2F75871%2F2011/PT
info:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBPD%2F96510%2F2013/PT
Document Type: Artigo em Revista Científica Internacional
Rights: openAccess
License: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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