Comprehensive constitutional genetic and epigenetic characterization of lynch-like individuals
dc.contributor.author | Damaso, Estela | |
dc.contributor.author | Gonzalez Acosta, Maribel | |
dc.contributor.author | Vargas Parra, Gardenia | |
dc.contributor.author | Navarro, Matilde | |
dc.contributor.author | Balmana, Judith | |
dc.contributor.author | Ramon y Cajal, Teresa | |
dc.contributor.author | Tuset, Noemi | |
dc.contributor.author | Thompson, Bryony A. | |
dc.contributor.author | Marin, Fátima | |
dc.contributor.author | Fernández, Anna | |
dc.contributor.author | Gómez, Carolina | |
dc.contributor.author | Velasco, Àngela | |
dc.contributor.author | Solanes, Ares | |
dc.contributor.author | Iglesias, Sílvia | |
dc.contributor.author | Urgel, Gisela | |
dc.contributor.author | López, Consol | |
dc.contributor.author | del Valle, Jesús | |
dc.contributor.author | Campos, Olga | |
dc.contributor.author | Santacana Espasa, Maria | |
dc.contributor.author | Matias-Guiu, Xavier | |
dc.contributor.author | Lázaro, Conxi | |
dc.contributor.author | Valle, Laura | |
dc.contributor.author | Brunet, Joan | |
dc.contributor.author | Pineda, Marta | |
dc.contributor.author | Capellà, Gabriel | |
dc.date.accessioned | 2020-12-11T14:48:40Z | |
dc.date.available | 2020-12-11T14:48:40Z | |
dc.date.issued | 2020 | |
dc.description.abstract | The causal mechanism for cancer predisposition in Lynch-like syndrome (LLS) remains unknown. Our aim was to elucidate the constitutional basis of mismatch repair (MMR) deficiency in LLS patients throughout a comprehensive (epi)genetic analysis. One hundred and fifteen LLS patients harboring MMR-deficient tumors and no germline MMR mutations were included. Mutational analysis of 26 colorectal cancer (CRC)-associated genes was performed. Pathogenicity of MMR variants was assessed by splicing and multifactorial likelihood analyses. Genome-wide methylome analysis was performed by the Infinium Human Methylation 450K Bead Chip. The multigene panel analysis revealed the presence of two MMR gene truncating mutations not previously found. Of a total of 15 additional MMR variants identified, five -present in 6 unrelated individuals- were reclassified as pathogenic. In addition, 13 predicted deleterious variants in other CRC-predisposing genes were found in 12 probands. Methylome analysis detected one constitutionalMLH1epimutation, but no additional differentially methylated regions were identified in LLS compared to LS patients or cancer-free individuals. In conclusion, the use of an ad-hoc designed gene panel combined with pathogenicity assessment of variants allowed the identification of deleterious MMR mutations as well as new LLS candidate causal genes. Constitutional epimutations in non-LS-associated genes are not responsible for LLS. | ca_ES |
dc.description.sponsorship | This work was funded by the Spanish Ministry of Economy and Competitiveness and cofunded by FEDER funds -a way to build Europe-(grants SAF2012-33636, SAF2015-68016-R and SAF2016-80888-R), CIBERONC, RTICC Network (RD12/0036/0031 and RD12/0036/0008), the Spanish Association Against Cancer (AECC) (080253), the Government of Catalonia (grant 2014SGR338, 2017SGR1282 and PERIS SLT002/16/0037), Fundacion Mutua Madrilena (grant AP114252013). We thank CERCA Programme for institutional support. ED was supported by a grant from the Spanish Ministry of Economy and Competitiveness. The AECC fellowship to MG-A. AF was supported by a grant from the Catalonian Health Department (SLT002/16/00409). FM was supported by CIBERONC. The Mexican National Council for Science and Technology (CONACyT) fellowship to GV. | ca_ES |
dc.identifier.doi | https://doi.org/10.3390/cancers12071799 | |
dc.identifier.idgrec | 034792 | |
dc.identifier.issn | 2072-6694 | |
dc.identifier.uri | http://hdl.handle.net/10459.1/70046 | |
dc.language.iso | eng | ca_ES |
dc.publisher | MDPI | ca_ES |
dc.relation.isformatof | Reproducció del document publicat a https://doi.org/10.3390/cancers12071799 | ca_ES |
dc.relation.ispartof | Cancers, 2020, vol. 12, núm. 7, p.1-25 | ca_ES |
dc.rights | cc-by (c) Damaso et al., 2020 | ca_ES |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | ca_ES |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.subject.other | Gens del càncer | ca_ES |
dc.subject.other | Recte--Càncer | ca_ES |
dc.subject.other | Mutació | ca_ES |
dc.title | Comprehensive constitutional genetic and epigenetic characterization of lynch-like individuals | ca_ES |
dc.type | info:eu-repo/semantics/article | ca_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | ca_ES |