| Literature DB >> 24184227 |
José Perea1, Daniel Rueda2, Alicia Canal2, Yolanda Rodríguez3, Edurne Álvaro4, Irene Osorio4, Cristina Alegre4, Bárbara Rivera5, Joaquín Martínez2, Javier Benítez6, Miguel Urioste6.
Abstract
An important proportion of early-onset colorectal cancer (CRC) does not show a hereditary component with limited knowledge about its molecular basis and features. We analyzed a subset of patients with early-onset CRC and compared them with patients with late-onset CRC. We analyzed the microsatellite instability and CpG island methylator phenotype (CIMP) in both populations and classified them into four molecular subtypes. We analyzed the differential features between groups. Only 12 of 81 early-onset cases (15%) showed microsatellite instability, 10 of which (83%) were Lynch syndrome cases; microsatellite instability cases in elderly patients were sporadic. Early-onset microsatellite-stable cases showed different tumor locations and more family history of cancer than the elderly. Microsatellite instability/CIMP-high early-onset CRC was associated with Lynch syndrome, whereas the elderly cases were associated with BRAF mutations. Early-onset microsatellite-stable/CIMP-high CRCs were more frequently mucinous and right sided than elderly cases, with a high incidence of Lynch syndrome neoplasms; early-onset microsatellite stable/CIMP-low/0 differed from elderly cases in location, stages, incidence of multiple primary neoplasms, and the familial component. The clinical and familial differences observed between early- and late-onset CRC when considering the different carcinogenetic pathways underline that the age at onset criterion should be considered when classifying CRC.Entities:
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Year: 2013 PMID: 24184227 DOI: 10.1016/j.jmoldx.2013.07.010
Source DB: PubMed Journal: J Mol Diagn ISSN: 1525-1578 Impact factor: 5.568