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dc.contributor.authorAntelo, Marina
dc.contributor.authorBalaguer, Francesc
dc.contributor.authorShia, Jinru
dc.contributor.authorShen, Yan
dc.contributor.authorHur, Keun
dc.contributor.authorMoreira, Leticia
dc.contributor.authorCuatrecasas, Miriam
dc.contributor.authorBujanda Fernández de Pierola, Luis
dc.contributor.authorGiraldez, María Dolores
dc.contributor.authorTakahashi, Masanobu
dc.contributor.authorCabanne, Ana
dc.contributor.authorBarugel, Mario Edmund
dc.contributor.authorArnold, Mildred
dc.contributor.authorRoca, Enrique Luis
dc.contributor.authorAndreu, Montserrat
dc.contributor.authorCastellvi-Bel, Sergi
dc.contributor.authorLlor, Xavier
dc.contributor.authorJover, Rodrigo
dc.contributor.authorCastells, Antoni
dc.contributor.authorBoland, C. Richard
dc.contributor.authorGoel, Ajay
dc.date.accessioned2014-02-21T19:21:15Z
dc.date.available2014-02-21T19:21:15Z
dc.date.issued2012-09-25
dc.identifier.citationPLoS ONE 7(9): (2012) // e45357es
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/10810/11611
dc.description12 p.es
dc.description.abstractObjective: Early-onset colorectal cancer (CRC) represents a clinically distinct form of CRC that is often associated with a poor prognosis. Methylation levels of genomic repeats such as LINE-1 elements have been recognized as independent factors for increased cancer-related mortality. The methylation status of LINE-1 elements in early-onset CRC has not been analyzed previously. -- Design: We analyzed 343 CRC tissues and 32 normal colonic mucosa samples, including 2 independent cohorts of CRC diagnosed <= 50 years old (n = 188), a group of sporadic CRC >50 years (MSS n = 89; MSI n = 46), and a group of Lynch syndrome CRCs (n = 20). Tumor mismatch repair protein expression, microsatellite instability status, LINE-1 and MLH1 methylation, somatic BRAF V600E mutation, and germline MUTYH mutations were evaluated. -- Results: Mean LINE-1 methylation levels (+/- SD) in the five study groups were early-onset CRC, 56.6% (8.6); sporadic MSI, 67.1% (5.5); sporadic MSS, 65.1% (6.3); Lynch syndrome, 66.3% (4.5) and normal mucosa, 76.5% (1.5). Early-onset CRC had significantly lower LINE-1 methylation than any other group (p<0.0001). Compared to patients with <65% LINE-1 methylation in tumors, those with >= 65% LINE-1 methylation had significantly better overall survival (p = 0.026, log rank test). -- Conclusions: LINE-1 hypomethylation constitutes a potentially important feature of early-onset CRC, and suggests a distinct molecular subtype. Further studies are needed to assess the potential of LINE-1 methylation status as a prognostic biomarker for young people with CRC.es
dc.description.sponsorshipThe present work was supported by grants R01 CA72851 and CA129286 from the National Cancer Institute, National Institutes of Health; and funds from the Baylor Research Institute to CRB and AG. FB was supported by a grant from Fundación Alfonso Martín Escudero and from Instituto de Salud Carlos III (PI10/00384). MA was supported by a “Type I Postgraduate Scholarship” given by the CONICET (National Council of Scientific and Technical Investigations) dependent on the Argentine Ministry of Science and Technology. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.es
dc.language.isoenges
dc.publisherPublic Library of Sciencees
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectchemical elementses
dc.subjectcolorectal canceres
dc.subjectchromosomal instabilityes
dc.subjectDNA methylationes
dc.subjectisland methylator phenotypees
dc.subjectlynch-syndromees
dc.subjectmicrosatellite instabilityes
dc.subjectmismatch repaires
dc.subjectmutationes
dc.subjectprognosises
dc.subjectprotein expressiones
dc.subjecttumor physiologyes
dc.titleA High Degree of LINE-1 Hypomethylation Is a Unique Feature of Early-Onset Colorectal Canceres
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© Antelo et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.es
dc.relation.publisherversionhttp://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0045357es
dc.identifier.doi10.1371/journal.pone.0045357
dc.departamentoesMedicinaes_ES
dc.departamentoeuMedikuntzaes_ES
dc.subject.categoriaAGRICULTURAL AND BIOLOGICAL SCIENCES
dc.subject.categoriaMEDICINE
dc.subject.categoriaBIOCHEMISTRY AND MOLECULAR BIOLOGY


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