Glycan analysis of colorectal cancer samples reveals stage-dependent changes in CEA glycosylation patterns

Carcinoembryonic antigen (CEA) is a glycoprotein associated with colorectal cancer (CRC). While the functions of its gene and protein have been fully characterized, its post-translational modifications in the context of CRC development remain undefined. To show the correlation between the different...

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Bibliographic Details
Published in:Clinical proteomics 2018-03, Vol.15 (1), p.9-11, Article 9
Main Authors: Zhao, Qianqian, Zhan, Tiancheng, Deng, Zaian, Li, Qianqian, Liu, Yaming, Yang, Shaojie, Ji, Dengbo, Li, Yan
Format: Article
Language:English
Subjects:
Analysis
Carcinoembryonic antigen
Colorectal cancer
Galactose
Glycosylation
Lectin microarray
Plant lectins
Polysaccharides
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Summary:Carcinoembryonic antigen (CEA) is a glycoprotein associated with colorectal cancer (CRC). While the functions of its gene and protein have been fully characterized, its post-translational modifications in the context of CRC development remain undefined. To show the correlation between the different stages of CRC development and changes in the glycosylation patterns of CEA, we analyzed CEA in tumor tissues (CEA-T) and paired tumor-adjacent normal tissues (CEA-A) from 53 colorectal cancer patients using a high-density lectin microarray containing 56 plant lectins. We detected higher expression levels of fucose, mannose and Thomsen-Friedenreich antigen, and lower expression levels of -acetylgalactosamine, -acetylglucosamine, galactose, branched and bisecting -glycans on CEA in the tumor tissues relative to the tumor-adjacent normal tissues. Furthermore, a combinatorial assessment of 9 lectins is sufficient to distinguish CRC tumor tissues from tumor-adjacent normal tissues with 83% sensitivity and ~ 90% specificity. Moreover, the levels of -acetylgalactosamine, mannose, galactose, -acetylglucosamine on CEA showed a downward trend after first experiencing an increase at Stage II with the stages of CRC. Our insights into the changing CEA glycosylation patterns and their role in the development of CRC highlight the importance of glycan variants on CEA for early clinical detection and staging of CRC.
ISSN:1542-6416
1559-0275
DOI:10.1186/s12014-018-9182-4