| Literature DB >> 26052075 |
Nuria Seguí1, Leonardo B Mina2, Conxi Lázaro1, Rebeca Sanz-Pamplona3, Tirso Pons4, Matilde Navarro1, Fernando Bellido1, Adriana López-Doriga3, Rafael Valdés-Mas5, Marta Pineda1, Elisabet Guinó3, August Vidal6, José Luís Soto7, Trinidad Caldés8, Mercedes Durán9, Miguel Urioste10, Daniel Rueda11, Joan Brunet12, Milagros Balbín13, Pilar Blay14, Silvia Iglesias1, Pilar Garré8, Enrique Lastra15, Ana Beatriz Sánchez-Heras16, Alfonso Valencia4, Victor Moreno17, Miguel Ángel Pujana18, Alberto Villanueva18, Ignacio Blanco1, Gabriel Capellá1, Jordi Surrallés2, Xose S Puente5, Laura Valle19.
Abstract
Identification of genes associated with hereditary cancers facilitates management of patients with family histories of cancer. We performed exome sequencing of DNA from 3 individuals from a family with colorectal cancer who met the Amsterdam criteria for risk of hereditary nonpolyposis colorectal cancer. These individuals had mismatch repair-proficient tumors and each carried nonsense variant in the FANCD2/FANCI-associated nuclease 1 gene (FAN1), which encodes a nuclease involved in DNA inter-strand cross-link repair. We sequenced FAN1 in 176 additional families with histories of colorectal cancer and performed in vitro functional analyses of the mutant forms of FAN1 identified. We detected FAN1 mutations in approximately 3% of families who met the Amsterdam criteria and had mismatch repair-proficient cancers with no previously associated mutations. These findings link colorectal cancer predisposition to the Fanconi anemia DNA repair pathway, supporting the connection between genome integrity and cancer risk.Entities:
Keywords: DNA Mismatch Repair; Genetic Risk Factor; Lynch Syndrome; Susceptibility
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Year: 2015 PMID: 26052075 DOI: 10.1053/j.gastro.2015.05.056
Source DB: PubMed Journal: Gastroenterology ISSN: 0016-5085 Impact factor: 22.682