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ZEB1 hypermethylation is associated with better prognosis in patients with colon cancer

dc.contributor.authorFernández García, V.
dc.contributor.authorCalvo, L.
dc.contributor.authorSuárez Seoane, Susana 
dc.contributor.authorMarcos, E.
dc.date.accessioned2024-08-26T08:33:13Z
dc.date.available2024-08-26T08:33:13Z
dc.date.issued2023
dc.identifier.citationClinical Epigenetics, 15(193), (2023); doi: 10.1186/s13148‑023‑01605‑7
dc.identifier.issn2072-4292
dc.identifier.urihttps://hdl.handle.net/10651/74169
dc.description.abstractColon cancer (CC) is a heterogeneous disease that is categorized into four Consensus Molecular Subtypes (CMS) according to gene expression. Patients with loco-regional CC (stages II/III) lack prognostic factors, making it essential to analyze new molecular markers that can delineate more aggressive tumors. Aberrant methylation of genes that are essential in crucial mechanisms such as epithelial mesenchymal transition (EMT) contributes to tumor progression in CC. We evaluate the presence of hyper- and hypomethylation in subrogate IHC markers used for CMS classification (CDX2, FRMD6, HTR2B, ZEB1) of 144 stage II/III patients and CC cell lines by pyrosequencing. ZEB1 expression was also studied in control and shRNA-silenced CC cell lines and in paired normal tissue/tumors by quantitative PCR. The pattern of ZEB1 staining was also analyzed in methylated/unmethylated tumors by immunohistochemistry.
dc.description.sponsorshipUniversidad Pública de Navarra; European Union Regional Development Fund (17–20, RefBioII, Trans‑Pyrenean cooperation network program 2016–2018, INTERREGPOCTEFA)
dc.language.isoeng
dc.relation.ispartofRemote Sensing
dc.rights© The Author(s) 2023.
dc.rightsCC Reconocimiento 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScopus
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85176134559&doi=10.3390%2frs15204930&partnerID=40&md5=87df6f7f7a8ba07f88624f12712b79b7
dc.titleZEB1 hypermethylation is associated with better prognosis in patients with colon cancer
dc.typejournal article
dc.identifier.doi10.1186/s13148‑023‑01605‑7
dc.relation.publisherversionhttp://dx.doi.org/10.1186/s13148-023-01605-7
dc.rights.accessRightsopen access
dc.type.hasVersionVoR


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