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dc.contributor.authorQuintanilla, Isabel
dc.contributor.authorLópez-Cerón, María
dc.contributor.authorJimeno, Mireya
dc.contributor.authorCuatrecasas, Miriam
dc.contributor.authorZabalza, Michel
dc.contributor.authorMoreira, Leticia
dc.contributor.authorAlonso, Virginia
dc.contributor.authorRodríguez de Miguel, Cristina
dc.contributor.authorMuñoz, Jennifer
dc.contributor.authorCastellvi-Bel, Sergi
dc.contributor.authorLlach, Josep
dc.contributor.authorCastells, Antoni
dc.contributor.authorBalaguer, Francesc
dc.contributor.authorCamps, Jordi
dc.contributor.authorPellisé, Maria
dc.date.accessioned2025-01-29T11:19:32Z
dc.date.available2025-01-29T11:19:32Z
dc.date.issued2019
dc.identifier.citationQuintanilla, Isabel; López-Cerón, María; Jimeno, Mireya [et al.]. Rectal Aberrant Crypt Foci in Humans Are Not Surrogate Markers for Colorectal Cancer Risk. Clinical and Translational Gastroenterology, 2019, 10(6), e00047. Disponible en: <https://journals.lww.com/ctg/fulltext/2019/06000/rectal_aberrant_crypt_foci_in_humans_are_not.6.aspx>. Fecha de acceso: 29 ene. 2025. DOI: 10.14309/ctg.0000000000000047ca
dc.identifier.issn2155-384Xca
dc.identifier.urihttp://hdl.handle.net/20.500.12328/4670
dc.description.abstractINTRODUCTION: Over the past 20 years, aberrant crypt foci (ACF) have emerged as potential precursors and biomarkers for colorectal cancer (CRC). However, data regarding their molecular pathogenesis, as well as their endoscopic and histological identification, remain inconsistent. METHODS: A wide cohort of ACF from 100 control subjects and 100 case patients, including patients with adenoma and CRC, were characterized for endoscopic, morphologic, and molecular features. RESULTS: We observed that among all the endoscopic features evaluated, only the number of large ACF correlated with CRC risk (P = 0.003), whereas the histological classification, as assessed by 2 different pathologists, was inconsistent and did not differ between control and case patients. Moreover, only a few APC and BRAF mutations and no microsatellite instability were detected in our samples. KRAS mutations were detected in 16.3% of ACF samples, which also exhibited increased MGMT hypermethylation. However, none of those events were found to be predictive of CRC risk. DISCUSSION: Although ACF might be preneoplastic lesions of the colon, they are not suitable biomarkers for assessing CRC progression.ca
dc.format.extent8ca
dc.language.isoengca
dc.publisherWolters Kluwerca
dc.relation.ispartofClinical and Translational Gastroenterologyca
dc.relation.ispartofseries10;6
dc.rights© 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterologyca
dc.subject.otherCàncer colorectalca
dc.subject.otherCáncer colorectalca
dc.subject.otherColorectal cancerca
dc.titleRectal Aberrant Crypt Foci in Humans Are Not Surrogate Markers for Colorectal Cancer Riskca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.subject.udc616ca
dc.identifier.doihttps://dx.doi.org/10.14309/ctg.0000000000000047ca


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