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dc.contributor.authorFernández-Ponce, Cecilia
dc.contributor.authorGeribaldi-Doldán, Noelia
dc.contributor.authorSánchez-Gomar, Ismael
dc.contributor.authorNavarro Quiroz, Roberto
dc.contributor.authorAtencio Ibarra, Linda
dc.contributor.authorGomez Escorcia, Lorena
dc.contributor.authorFernández-Cisnal, Ricardo
dc.contributor.authorAroca Martinez, Gustavo
dc.contributor.authorGarcía-Cózar, Francisco
dc.contributor.authorNavarro Quiroz, Elkin
dc.date.accessioned2021-05-31T18:52:24Z
dc.date.available2021-05-31T18:52:24Z
dc.date.issued2021
dc.identifier.issn14220067
dc.identifier.urihttps://hdl.handle.net/20.500.12442/7846
dc.description.abstractColorectal cancer (CRC) is one of the main causes of cancer death in the world. Post-translational modifications (PTMs) have been extensively studied in malignancies due to its relevance in tumor pathogenesis and therapy. This review is focused on the dysregulation of glycosyltransferase expression in CRC and its impact in cell function and in several biological pathways associated with CRC pathogenesis, prognosis and therapeutic approaches. Glycan structures act as interface molecules between cells and their environment and in several cases facilitate molecule function. CRC tissue shows alterations in glycan structures decorating molecules, such as annexin-1, mucins, heat shock protein 90 (Hsp90), β1 integrin, carcinoembryonic antigen (CEA), epidermal growth factor receptor (EGFR), insulin-like growth factor-binding protein 3 (IGFBP3), transforming growth factor beta (TGF-β) receptors, Fas (CD95), PD-L1, decorin, sorbin and SH3 domain-containing protein 1 (SORBS1), CD147 and glycosphingolipids. All of these are described as key molecules in oncogenesis and metastasis. Therefore, glycosylation in CRC can affect cell migration, cell–cell adhesion, actin polymerization, mitosis, cell membrane repair, apoptosis, cell differentiation, stemness regulation, intestinal mucosal barrier integrity, immune system regulation, T cell polarization and gut microbiota composition; all such functions are associated with the prognosis and evolution of the disease. According to these findings, multiple strategies have been evaluated to alter oligosaccharide processing and to modify glycoconjugate structures in order to control CRC progression and prevent metastasis. Additionally, immunotherapy approaches have contemplated the use of neoantigens, generated by altered glycosylation, as targets for tumor-specific T cells or engineered CAR (Chimeric antigen receptors) T cells.eng
dc.format.mimetypepdfspa
dc.language.isoengeng
dc.publisherMDPIeng
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceInternational Journal of Molecular Sciencieseng
dc.sourceVol. 22 Nº 11, (2021)
dc.subjectColorectal cancereng
dc.subjectGlycosyl transferaseeng
dc.subjectGlycosylationeng
dc.subjectPost-translational modificationeng
dc.titleThe role of glycosyltransferases in colorectal cancereng
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