PloS one · 2014
The MLH1 c.1852_1853delinsGC (p.K618A) variant in colorectal cancer: genetic association study in 18,723 individuals.
Клиническое исследованиеСтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Abulí Anna, Bujanda Luis, Muñoz Jenifer, Buch Stephan, Schafmayer Clemens, Valeria Maiorana Maria, Veneroni Silvia, van Wezel Tom, Liu Tao, Westers Helga, Esteban-Jurado Clara, Ocaña Teresa, Piqué Josep M, Andreu Montserrat, Jover Rodrigo, Carracedo Angel, Xicola Rosa M, Llor Xavier, Castells Antoni, EPICOLON Consortium, Dunlop Malcolm, Hofstra Robert, Lindblom Annika, Wijnen Juul, Peterlongo Paolo, Hampe Jochen, Ruiz-Ponte Clara, Castellví-Bel Sergi
Аннотация
Colorectal cancer is one of the most frequent neoplasms and an important cause of mortality in the developed world. Mendelian syndromes account for about 5% of the total burden of CRC, being Lynch syndrome and familial adenomatous polyposis the most common forms. Lynch syndrome tumors develop mainly as a consequence of defective DNA mismatch repair associated with germline mutations in MLH1, MSH2, MSH6 and PMS2. A significant proportion of variants identified by screening these genes correspond to missense or noncoding changes without a clear pathogenic consequence, and they are designated as "variants of uncertain significance", being the c.1852_1853delinsGC (p.K618A) variant in the MLH1 gene a clear example. The implication of this variant as a low-penetrance risk variant for CRC was assessed in the present study by performing a case-control study within a large cohort from the COGENT consortium-COST Action BM1206 including 18,723 individuals (8,055 colorectal cancer cases and 10,668 controls) and a case-only genotype-phenotype correlation with several clinical and pathological characteristics restricted to the Epicolon cohort. Our results showed no involvement of this variant as a low-penetrance variant for colorectal cancer genetic susceptibility and no association with any clinical and pathological characteristics including family history for this neoplasm or Lynch syndrome.
Предметные рубрики MeSH
Adaptor Proteins, Signal TransducingAdenosine TriphosphatasesAmino Acid SubstitutionCohort StudiesColorectal NeoplasmsDNA Repair EnzymesDNA-Binding ProteinsFemaleGenetic Association StudiesGerm-Line MutationHumansINDEL MutationMaleMismatch Repair Endonuclease PMS2MutL Protein Homolog 1MutS Homolog 2 ProteinMutation, MissenseNuclear Proteins