(Sialyl)Lewis Antigen Expression on Glycosphingolipids, N-, and O-Glycans in Colorectal Cancer Cell Lines is Linked to a Colon-Like Differentiation Program

被引:1
|
作者
Wang, Di [1 ]
Maduni, Katarina [1 ,2 ]
Mayboroda, Oleg A. [1 ]
Lageveen-Kammeijer, Guinevere S. M. [1 ,3 ]
Wuhrer, Manfred [1 ]
机构
[1] Leiden Univ Med Ctr, Ctr Prote & Metabol, Leiden, Netherlands
[2] Univ Copenhagen, Copenhagen Ctr Glyc, Dept Cellular & Mol Med, Copenhagen, Denmark
[3] Univ Groningen, Groningen Res Inst Pharm, Div Analyt Biochem, Groningen, Netherlands
关键词
SIALYL-LEWIS-X; HUMAN ALPHA(1,3)FUCOSYLTRANSFERASE GENE; FUCOSYL-TRANSFERASE GENE; MOLECULAR-CLONING; MESSENGER-RNA; E-SELECTIN; ALPHA 2,3-SIALYLTRANSFERASE; DETERMINES EXPRESSION; CARCINOMA CELLS; AMINO-ACIDS;
D O I
10.1016/j.mcpro.2024.100776
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Alterations in the glycomic profile are a hallmark of cancer, including colorectal cancer (CRC). While, the glycosylation of glycoproteins and glycolipids has been widely studied for CRC cell lines and tissues, a comprehensive overview of CRC glycomics is still lacking due to the usage of different samples and analytical methods. In this study, we compared glycosylation features of N-, O-glycans, and glycosphingolipid glycans for a set of 22 CRC cell lines, all measured by porous graphitized carbon nano-liquid chromatography-tandem mass spectrometry. An overall, high abundance of (sialyl)Lewis antigens for colon-like cell lines was found, while undifferentiated cell lines showed high expression of H blood group antigens and alpha 2-3/6 sialylation. Moreover, significant associations of glycosylation features were found between the three classes of glycans, such as (sialyl)Lewis and H blood group antigens. Integration of the datasets with transcriptomics data revealed positive correlations between (sialyl)Lewis antigens, the corresponding glycosyltransferase FUT3 and transcription factors CDX1, ETS, HNF1/4A, MECOM, and MYB. This indicates a possible role of these transcription factors in the upregulation of (sialyl)Lewis antigens, particularly on glycosphingolipid glycans, via FUT3/4 expression in colon-like cell lines. In conclusion, our study provides insights into the possible regulation of glycans in CRC and can serve as a guide for the development of diagnostic and therapeutic biomarkers.
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页数:14
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