Literature DB >> 17039269

Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies.

R C Green1, J S Green, S K Buehler, J D Robb, D Daftary, S Gallinger, J R McLaughlin, P S Parfrey, H B Younghusband.   

Abstract

Newfoundland has the highest rate of colorectal cancer (CRC) of any Canadian province. In order to investigate the factors, especially genetic components, responsible for CRC we established the Newfoundland Colorectal Cancer Registry. In a 5-year period we examined every case of CRC diagnosed under the age of 75 years and obtained consent from 730 cases. Careful analysis of family history was used to assign a familial cancer risk, based on established criteria. We observed that 3.7% of CRC cases came from families meeting the Amsterdam II criteria and a further 0.9% of cases involved familial adenomatous polyposis (FAP). An additional 43% of cases met one or more of the revised Bethesda criteria and 31% of all cases had a first-degree relative affected with CRC. We compared the Newfoundland data with data from the province of Ontario, where the same recruitment and risk-assessment criteria were used. In all categories, the indicators of familial risk were significantly higher in Newfoundland. These data were also compared to results published from 13 other population-based studies worldwide. In every category the proportion of Newfoundland cases meeting the criteria was higher than in any other population. The mean differences were: 3.5-fold greater for FAP, 2.8-fold higher for Amsterdam criteria, 2.0-fold higher for Bethesda criteria and 1.9-fold higher for the number of affected first-degree relatives. We conclude that the high incidence of CRC in Newfoundland may be attributable to genetic, or at least familial, factors. In the high-risk families we provide evidence for the involvement of founder mutations in the APC and MSH2 genes.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17039269     DOI: 10.1007/s10689-006-9104-x

Source DB:  PubMed          Journal:  Fam Cancer        ISSN: 1389-9600            Impact factor:   2.375


  46 in total

1.  A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO.

Authors:  D G R Evans; D M Eccles; N Rahman; K Young; M Bulman; E Amir; A Shenton; A Howell; F Lalloo
Journal:  J Med Genet       Date:  2004-06       Impact factor: 6.318

2.  The identical 5' splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect.

Authors:  L Spirio; J Green; J Robertson; M Robertson; B Otterud; J Sheldon; E Howse; R Green; J Groden; R White; M Leppert
Journal:  Hum Genet       Date:  1999-11       Impact factor: 4.132

3.  Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from Newfoundland.

Authors:  S E Olufemi; J S Green; P Manickam; S C Guru; S K Agarwal; M B Kester; Q Dong; A L Burns; A M Spiegel; S J Marx; F S Collins; S C Chandrasekharappa
Journal:  Hum Mutat       Date:  1998       Impact factor: 4.878

4.  Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: later age of onset.

Authors:  Heather Hampel; Julie A Stephens; Eero Pukkala; Risto Sankila; Lauri A Aaltonen; Jukka-Pekka Mecklin; Albert de la Chapelle
Journal:  Gastroenterology       Date:  2005-08       Impact factor: 22.682

5.  Frequency of hereditary non-polyposis colorectal cancer among Uruguayan patients with colorectal cancer.

Authors:  C Sarroca; A Della Valle; R Fresco; E Renkonen; P Peltömaki; Ht Lynch
Journal:  Clin Genet       Date:  2005-07       Impact factor: 4.438

6.  Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis.

Authors:  M P de Leon; M Pedroni; P Benatti; A Percesepe; C Di Gregorio; M Foroni; G Rossi; M Genuardi; G Neri; F Leonardi; A Viel; E Capozzi; M Boiocchi; L Roncucci
Journal:  Gut       Date:  1999-07       Impact factor: 23.059

7.  The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas.

Authors:  J M Cunningham; C Y Kim; E R Christensen; D J Tester; Y Parc; L J Burgart; K C Halling; S K McDonnell; D J Schaid; C Walsh Vockley; V Kubly; H Nelson; V V Michels; S N Thibodeau
Journal:  Am J Hum Genet       Date:  2001-08-24       Impact factor: 11.025

8.  Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk.

Authors:  Marina E Croitoru; Sean P Cleary; Nando Di Nicola; Michael Manno; Teresa Selander; Melyssa Aronson; Mark Redston; Michelle Cotterchio; Julia Knight; Robert Gryfe; Steven Gallinger
Journal:  J Natl Cancer Inst       Date:  2004-11-03       Impact factor: 13.506

9.  Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients.

Authors:  L A Aaltonen; P Peltomäki; J P Mecklin; H Järvinen; J R Jass; J S Green; H T Lynch; P Watson; G Tallqvist; M Juhola
Journal:  Cancer Res       Date:  1994-04-01       Impact factor: 12.701

10.  Frequency of hereditary nonpolyposis colorectal cancer. A prospective multicenter study in Finland.

Authors:  J P Mecklin; H J Järvinen; A Hakkiluoto; H Hallikas; K M Hiltunen; N Härkönen; I Kellokumpu; S Laitinen; J Ovaska; J Tulikoura
Journal:  Dis Colon Rectum       Date:  1995-06       Impact factor: 4.585

View more
  43 in total

1.  Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer.

Authors:  Aung Ko Win; Sean P Cleary; James G Dowty; John A Baron; Joanne P Young; Daniel D Buchanan; Melissa C Southey; Terrilea Burnett; Patrick S Parfrey; Roger C Green; Loïc Le Marchand; Polly A Newcomb; Robert W Haile; Noralane M Lindor; John L Hopper; Steven Gallinger; Mark A Jenkins
Journal:  Int J Cancer       Date:  2011-04-08       Impact factor: 7.396

2.  Genetic structure of the Newfoundland and Labrador population: founder effects modulate variability.

Authors:  Guangju Zhai; Jiayi Zhou; Michael O Woods; Jane S Green; Patrick Parfrey; Proton Rahman; Roger C Green
Journal:  Eur J Hum Genet       Date:  2015-12-16       Impact factor: 4.246

3.  Public attitudes towards genomic risk profiling as a component of routine population screening.

Authors:  S G Nicholls; B J Wilson; S M Craigie; H Etchegary; D Castle; J C Carroll; B K Potter; L Lemyre; J Little
Journal:  Genome       Date:  2013-08-31       Impact factor: 2.166

4.  Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from Newfoundland.

Authors:  Daniel R Evans; Jane S Green; Michael O Woods
Journal:  Fam Cancer       Date:  2018-04       Impact factor: 2.375

5.  The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease.

Authors:  M O Woods; H B Younghusband; P S Parfrey; S Gallinger; J McLaughlin; E Dicks; S Stuckless; A Pollett; B Bapat; M Mrkonjic; A de la Chapelle; M Clendenning; S N Thibodeau; M Simms; A Dohey; P Williams; D Robb; C Searle; J S Green; R C Green
Journal:  Gut       Date:  2010-08-03       Impact factor: 23.059

6.  Universal tumor screening for Lynch syndrome: perspectives of Canadian pathologists and genetic counselors.

Authors:  Elizabeth Dicks; Daryl Pullman; Ken Kao; Andrée MacMillan; Charlene Simmonds; Holly Etchegary
Journal:  J Community Genet       Date:  2018-11-21

7.  Consulting the community: public expectations and attitudes about genetics research.

Authors:  Holly Etchegary; Jane Green; Elizabeth Dicks; Daryl Pullman; Catherine Street; Patrick Parfrey
Journal:  Eur J Hum Genet       Date:  2013-04-17       Impact factor: 4.246

8.  Vitamin D intake is negatively associated with promoter methylation of the Wnt antagonist gene DKK1 in a large group of colorectal cancer patients.

Authors:  James B Rawson; Zhouyu Sun; Elizabeth Dicks; Darshana Daftary; Patrick S Parfrey; Roger C Green; Steven Gallinger; John R McLaughlin; Peizhong P Wang; Julia A Knight; Bharati Bapat
Journal:  Nutr Cancer       Date:  2012-09-11       Impact factor: 2.900

9.  Literacy assessment of family health history tools for public health prevention.

Authors:  C Wang; R E Gallo; L Fleisher; S M Miller
Journal:  Public Health Genomics       Date:  2010-01-04       Impact factor: 2.000

10.  Community engagement with genetics: public perceptions and expectations about genetics research.

Authors:  Holly Etchegary; Jane Green; Patrick Parfrey; Catherine Street; Daryl Pullman
Journal:  Health Expect       Date:  2013-08-23       Impact factor: 3.377

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.