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dc.contributor.authorBasnet, Suyog
dc.contributor.authorVallenari, Evan Michael
dc.contributor.authorMaharjan, Urusha
dc.contributor.authorSharma, Sunita
dc.contributor.authorSchreurs, Olaf Joseph Franciscus
dc.contributor.authorSapkota, Dipak
dc.date.accessioned2024-02-23T08:14:26Z
dc.date.available2024-02-23T08:14:26Z
dc.date.created2023-07-08T15:41:18Z
dc.date.issued2023
dc.identifier.issn2218-273X
dc.identifier.urihttps://hdl.handle.net/11250/3119515
dc.description.abstractS100A16 is a member of the S100 protein family. S100A16 is expressed in a variety of human tissues, although at varying levels. S100A16 expression is especially high in tissues rich in epithelial cells. mRNA and protein levels of S100A16 have been reported to be differentially expressed in the majority of human cancers. Functionally, S100A16 has been linked to several aspects of tumorigenesis, for example, cell proliferation, differentiation, migration, invasion, and epithelial-mesenchymal transition (EMT). Accordingly, S100A16 has been suggested to have both tumour-promoting and suppressive roles in human cancers. S100A16-mediated cellular functions are suggested to be mediated by the regulation of various signaling pathways/proteins including EMT-related proteins E-cadherin and Vimentin, PI3K-AKT, p53, MMP1-1, MMP-2, MMP-9, JNK/p38, etc. In addition to the functional roles, expression of S100A16 has been suggested to have prognostic potential in various cancer types. The aims of this review are to summarise the expression profile, identify common molecular partners and functional roles, and explore the prognostic potential of S100A16 in human cancers.en_US
dc.language.isoengen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectS100en_US
dc.subjectEMTen_US
dc.subjectprognosisen_US
dc.subjectbiomarkersen_US
dc.subjectproliferationen_US
dc.subjectinvasionen_US
dc.titleAn Update on S100A16 in Human Canceren_US
dc.title.alternativeAn Update on S100A16 in Human Canceren_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright: © 2023 by the authors. Licensee MDPI, Basel, Switzerland.en_US
dc.subject.nsiVDP::Medisinske Fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710::Medisinsk molekylærbiologi: 711en_US
dc.source.volume13en_US
dc.source.journalBiomoleculesen_US
dc.source.issue7en_US
dc.identifier.doihttps://doi.org/10.3390/biom13071070
dc.identifier.cristin2161527
dc.source.articlenumber1070en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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