Literature DB >> 33118316

FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factor.

Lisa A Cannon-Albright1,2, Craig C Teerlink1, Jeffrey Stevens1, Angela K Snow2, Bryony A Thompson2,3, Russell Bell2, Kim N Nguyen1, Nykole R Sargent2, Wendy K Kohlmann2, Deborah W Neklason1,2, Sean V Tavtigian2,4.   

Abstract

PURPOSE: While familial aggregation of colorectal cancer (CRC) is recognized, the majority of the germline predisposition factors remain unidentified, and many high-risk CRC pedigrees remain unexplained by known risk variants. Fanconi Anemia genes have been recognized to be associated with cancer risk. Notably, FANCM (OMIM 609644) variants have been reported to confer risk for CRC and breast cancer.
METHODS: Exome sequencing of CRC-affected cousins in a set of 47 independent extended high-risk CRC pedigrees identified a candidate set of rare, shared variants. Variants were tested for association with risk in 744 Utah CRC cases and 1525 controls, and for segregation with CRC in affected relatives.
RESULTS: A FANCM stopgain variant was observed in two CRC-affected cousin pairs, each from an independent Utah high-risk pedigree, and yielded a nonsignificant, but elevated OR = 2.05 in a set of Utah cases and controls. Segregation of the variant to other related CRC-affected cases was observed in the two extended pedigrees.
CONCLUSION: A rare stopgain variant in FANCM (rs144567652) that is recognized as a breast cancer predisposition variant, and that has previously been proposed, but not confirmed, as a CRC predisposition variant, is validated here as a risk factor for familial CRC.
© 2020 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC.

Entities:  

Keywords:  zzm321990FANCMzzm321990; UPDB; colorectal cancer; high-risk pedigree

Mesh:

Substances:

Year:  2020        PMID: 33118316      PMCID: PMC7767553          DOI: 10.1002/mgg3.1532

Source DB:  PubMed          Journal:  Mol Genet Genomic Med        ISSN: 2324-9269            Impact factor:   2.183


  25 in total

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Authors:  Ani Manichaikul; Josyf C Mychaleckyj; Stephen S Rich; Kathy Daly; Michèle Sale; Wei-Min Chen
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2.  Colonic adenoma risk in familial colorectal cancer--a study of six extended kindreds.

Authors:  Deborah W Neklason; Brett L Thorpe; Angel Ferrandez; Anil Tumbapura; Kenneth Boucher; Gilda Garibotti; Richard A Kerber; Cindy H Solomon; Wade S Samowitz; John C Fang; Geraldine P Mineau; Mark F Leppert; Randall W Burt; Scott K Kuwada
Journal:  Am J Gastroenterol       Date:  2008-07-30       Impact factor: 10.864

3.  FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.

Authors:  Paolo Peterlongo; Irene Catucci; Mara Colombo; Laura Caleca; Eliseos Mucaki; Massimo Bogliolo; Maria Marin; Francesca Damiola; Loris Bernard; Valeria Pensotti; Sara Volorio; Valentina Dall'Olio; Alfons Meindl; Claus Bartram; Christian Sutter; Harald Surowy; Valérie Sornin; Marie-Gabrielle Dondon; Séverine Eon-Marchais; Dominique Stoppa-Lyonnet; Nadine Andrieu; Olga M Sinilnikova; Gillian Mitchell; Paul A James; Ella Thompson; Marina Marchetti; Cristina Verzeroli; Carmen Tartari; Gabriele Lorenzo Capone; Anna Laura Putignano; Maurizio Genuardi; Veronica Medici; Isabella Marchi; Massimo Federico; Silvia Tognazzo; Laura Matricardi; Simona Agata; Riccardo Dolcetti; Lara Della Puppa; Giulia Cini; Viviana Gismondi; Valeria Viassolo; Chiara Perfumo; Maria Antonietta Mencarelli; Margherita Baldassarri; Bernard Peissel; Gaia Roversi; Valentina Silvestri; Piera Rizzolo; Francesca Spina; Caterina Vivanet; Maria Grazia Tibiletti; Maria Adelaide Caligo; Gaetana Gambino; Stefania Tommasi; Brunella Pilato; Carlo Tondini; Chiara Corna; Bernardo Bonanni; Monica Barile; Ana Osorio; Javier Benitez; Luisa Balestrino; Laura Ottini; Siranoush Manoukian; Marco A Pierotti; Alessandra Renieri; Liliana Varesco; Fergus J Couch; Xianshu Wang; Peter Devilee; Florentine S Hilbers; Christi J van Asperen; Alessandra Viel; Marco Montagna; Laura Cortesi; Orland Diez; Judith Balmaña; Jan Hauke; Rita K Schmutzler; Laura Papi; Miguel Angel Pujana; Conxi Lázaro; Anna Falanga; Kenneth Offit; Joseph Vijai; Ian Campbell; Barbara Burwinkel; Anders Kvist; Hans Ehrencrona; Sylvie Mazoyer; Sara Pizzamiglio; Paolo Verderio; Jordi Surralles; Peter K Rogan; Paolo Radice
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4.  ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.

Authors:  Kai Wang; Mingyao Li; Hakon Hakonarson
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5.  Dominant inheritance of adenomatous colonic polyps and colorectal cancer.

Authors:  R W Burt; D T Bishop; L A Cannon; M A Dowdle; R G Lee; M H Skolnick
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6.  A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data.

Authors:  Hao Hu; Jared C Roach; Hilary Coon; Stephen L Guthery; Karl V Voelkerding; Rebecca L Margraf; Jacob D Durtschi; Sean V Tavtigian; Wilfred Wu; Paul Scheet; Shuoguo Wang; Jinchuan Xing; Gustavo Glusman; Robert Hubley; Hong Li; Vidu Garg; Barry Moore; Leroy Hood; David J Galas; Deepak Srivastava; Martin G Reese; Lynn B Jorde; Mark Yandell; Chad D Huff
Journal:  Nat Biotechnol       Date:  2014-05-18       Impact factor: 54.908

7.  A framework for variation discovery and genotyping using next-generation DNA sequencing data.

Authors:  Mark A DePristo; Eric Banks; Ryan Poplin; Kiran V Garimella; Jared R Maguire; Christopher Hartl; Anthony A Philippakis; Guillermo del Angel; Manuel A Rivas; Matt Hanna; Aaron McKenna; Tim J Fennell; Andrew M Kernytsky; Andrey Y Sivachenko; Kristian Cibulskis; Stacey B Gabriel; David Altshuler; Mark J Daly
Journal:  Nat Genet       Date:  2011-04-10       Impact factor: 38.330

8.  The variant call format and VCFtools.

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Journal:  Bioinformatics       Date:  2011-06-07       Impact factor: 6.937

9.  The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer.

Authors:  Clara Esteban-Jurado; Sebastià Franch-Expósito; Jenifer Muñoz; Teresa Ocaña; Sabela Carballal; Maria López-Cerón; Miriam Cuatrecasas; Maria Vila-Casadesús; Juan José Lozano; Enric Serra; Sergi Beltran; Alejandro Brea-Fernández; Clara Ruiz-Ponte; Antoni Castells; Luis Bujanda; Pilar Garre; Trinidad Caldés; Joaquín Cubiella; Francesc Balaguer; Sergi Castellví-Bel
Journal:  Eur J Hum Genet       Date:  2016-05-11       Impact factor: 4.246

10.  Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.

Authors:  Francisco Javier Gracia-Aznarez; Victoria Fernandez; Guillermo Pita; Paolo Peterlongo; Orlando Dominguez; Miguel de la Hoya; Mercedes Duran; Ana Osorio; Leticia Moreno; Anna Gonzalez-Neira; Juan Manuel Rosa-Rosa; Olga Sinilnikova; Sylvie Mazoyer; John Hopper; Conchi Lazaro; Melissa Southey; Fabrice Odefrey; Siranoush Manoukian; Irene Catucci; Trinidad Caldes; Henry T Lynch; Florentine S M Hilbers; Christi J van Asperen; Hans F A Vasen; David Goldgar; Paolo Radice; Peter Devilee; Javier Benitez
Journal:  PLoS One       Date:  2013-02-08       Impact factor: 3.240

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  2 in total

1.  An intronic variant in the CELF4 gene is associated with risk for colorectal cancer.

Authors:  Craig C Teerlink; Jeff Stevens; Rolando Hernandez; Julio C Facelli; Lisa A Cannon-Albright
Journal:  Cancer Epidemiol       Date:  2021-04-28       Impact factor: 2.890

Review 2.  Fanconi Anemia Pathway in Colorectal Cancer: A Novel Opportunity for Diagnosis, Prognosis and Therapy.

Authors:  Fatemeh Ghorbani Parsa; Stefania Nobili; Mina Karimpour; Hamid Asadzadeh Aghdaei; Ehsan Nazemalhosseini-Mojarad; Enrico Mini
Journal:  J Pers Med       Date:  2022-03-04
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