Candidate predisposing germline copy number variants in early onset colorectal cancer patients View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2017-05

AUTHORS

A. J. Brea-Fernandez, C. Fernandez-Rozadilla, M. Alvarez-Barona, D. Azuara, M. M. Ginesta, J. Clofent, L. de Castro, D. Gonzalez, M. Andreu, X. Bessa, X. Llor, R. Xicola, R. Jover, A. Castells, S. Castellvi-Bel, G. Capella, A. Carracedo, C. Ruiz-Ponte

ABSTRACT

PURPOSE: A great proportion of the heritability of colorectal cancer (CRC) still remains unexplained, and rare variants, as well as copy number changes, have been proposed as potential candidates to explain the so-called 'missing heritability'. We aimed to identify rare high-to-moderately penetrant copy number variants (CNVs) in patients suspected of having hereditary CRC due to an early onset. METHODS/PATIENTS: We have selected for genome-wide copy number analysis, 27 MMR-proficient early onset CRC patients (<50 years) without identifiable germline mutations in Mendelian genes related to this phenotype. Rare CNVs were selected by removing all CNVs detected at MAF >1% in the in-house control CNV database (n = 629 healthy controls). Copy number assignment was checked by duplex real-time quantitative PCR or multiplex ligation probe amplification. Somatic mutation analysis in candidate genes included: loss of heterozygosity studies, point mutation screening, and methylation status of the promoter. RESULTS: We have identified two rare germline deletions involving the AK3 and SLIT2 genes in two patients. The search for a second somatic mutational event in the corresponding CRC tumors showed loss of heterozygosity in AK3, and promoter hypermethylation in SLIT2. Both genes have been previously related to colorectal carcinogenesis. CONCLUSIONS: These findings suggest that AK3 and SLIT2 may be potential candidates involved in genetic susceptibility to CRC. More... »

PAGES

625-632

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s12094-016-1576-z

DOI

http://dx.doi.org/10.1007/s12094-016-1576-z

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1014235691

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/27888432


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