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dc.contributor.authorKaragiorgou, Zoi
dc.contributor.authorFountas, Panagiotis N
dc.contributor.authorManou, Dimitra
dc.contributor.authorKnutsen, Erik
dc.contributor.authorTheocharis, Achilleas D.
dc.date.accessioned2023-01-10T11:39:55Z
dc.date.available2023-01-10T11:39:55Z
dc.date.issued2022-10-29
dc.description.abstractProteoglycans (PGs) are pivotal components of extracellular matrices, involved in a variety of processes such as migration, invasion, morphogenesis, differentiation, drug resistance, and epithelial-to-mesenchymal transition (EMT). Cellular plasticity is a crucial intermediate phenotypic state acquired by cancer cells, which can modulate EMT and the generation of cancer stem cells (CSCs). PGs affect cell plasticity, stemness, and EMT, altering the cellular shape and functions. PGs control these functions, either by direct activation of signaling cascades, acting as co-receptors, or through regulation of the availability of biological compounds such as growth factors and cytokines. Differential expression of microRNAs is also associated with the expression of PGs and their interplay is implicated in the fine tuning of cancer cell phenotype and potential. This review summarizes the involvement of PGs in the regulation of EMT and stemness of cancer cells and highlights the molecular mechanisms.en_US
dc.identifier.citationKaragiorgou, Fountas, Manou, Knutsen E, Theocharis AD. Proteoglycans Determine the Dynamic Landscape of EMT and Cancer Cell Stemness. Cancers. 2022;14(21)en_US
dc.identifier.cristinIDFRIDAID 2077181
dc.identifier.doi10.3390/cancers14215328
dc.identifier.issn2072-6694
dc.identifier.urihttps://hdl.handle.net/10037/28110
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.relation.journalCancers
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2022 The Author(s)en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.rightsAttribution 4.0 International (CC BY 4.0)en_US
dc.titleProteoglycans Determine the Dynamic Landscape of EMT and Cancer Cell Stemnessen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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Attribution 4.0 International (CC BY 4.0)
Med mindre det står noe annet, er denne innførselens lisens beskrevet som Attribution 4.0 International (CC BY 4.0)