Literature DB >> 10483990

Genetic testing in hereditary colorectal cancer: indications and procedures.

J P Terdiman1, P G Conrad, M H Sleisenger.   

Abstract

Approximately 25% of colorectal cancers occur in younger individuals or those with a personal or family history of the disease, suggesting a heritable susceptibility. The minority of these cases are accounted for by one of the well-described hereditary colorectal cancer syndromes, familial adenomatous polyposis (FAP) and hereditary nonpolyposis colorectal cancer (HNPCC). The recent identification and cloning of the genes responsible for FAP and HNPCC, along with other colon cancer susceptibility genes, has led to the wide-spread availability of genetic testing for hereditary colorectal cancer. Genetic testing raises clinical, ethical, legal, and psychosocial questions that must urgently be discussed. This review highlights areas of knowledge and uncertainty about genetic predisposition testing for colorectal cancer and provides clinicians with practical recommendations regarding the proper indications and procedures for this testing.

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Year:  1999        PMID: 10483990     DOI: 10.1111/j.1572-0241.1999.01356.x

Source DB:  PubMed          Journal:  Am J Gastroenterol        ISSN: 0002-9270            Impact factor:   10.864


  12 in total

Review 1.  Molecular basis for subdividing hereditary colon cancer?

Authors:  W M Grady
Journal:  Gut       Date:  2005-12       Impact factor: 23.059

2.  Cascade genetic testing for mismatch repair gene mutations.

Authors:  R J Mitchell; R K Ferguson; A Macdonald; M G Dunlop; H Campbell; M E Porteous
Journal:  Fam Cancer       Date:  2008-04-04       Impact factor: 2.375

3.  Evidence of linkage to chromosomes 10p15.3-p15.1, 14q24.3-q31.1 and 9q33.3-q34.3 in non-syndromic colorectal cancer families.

Authors:  Ian W Saunders; Jason Ross; Finlay Macrae; Graeme P Young; Ignacio Blanco; Jesper Brohede; Glenn Brown; Diana Brookes; Trevor Lockett; Peter L Molloy; Victor Moreno; Gabriel Capella; Garry N Hannan
Journal:  Eur J Hum Genet       Date:  2011-08-10       Impact factor: 4.246

4.  Dietary factors, genetic and epigenetic influences in colorectal cancer.

Authors:  M L Pellegrini; P Argibay; D E Gomez
Journal:  Exp Ther Med       Date:  2010-03-01       Impact factor: 2.447

5.  The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome.

Authors:  Susan Stuckless; Patrick S Parfrey; Michael O Woods; Janet Cox; G William Fitzgerald; Jane S Green; Roger C Green
Journal:  Fam Cancer       Date:  2007       Impact factor: 2.375

6.  Clinicopathological and molecular genetic analysis of 4 typical Chinese HNPCC families.

Authors:  Q Cai; M H Sun; H F Lu; T M Zhang; S J Mo; Y Xu; S J Cai; X Z Zhu; D R Shi
Journal:  World J Gastroenterol       Date:  2001-12       Impact factor: 5.742

7.  Pathogenicity of missense and splice site mutations in hMSH2 and hMLH1 mismatch repair genes: implications for genetic testing.

Authors:  M Cravo; A J Afonso; P Lage; C Albuquerque; L Maia; C Lacerda; P Fidalgo; P Chaves; C Cruz; C Nobre-Leitão
Journal:  Gut       Date:  2002-03       Impact factor: 23.059

Review 8.  Impact of genetic risk assessment on nutrition-related lifestyle behaviours.

Authors:  Jacqueline A Vernarelli
Journal:  Proc Nutr Soc       Date:  2012-10-25       Impact factor: 6.297

9.  Hopefulness predicts resilience after hereditary colorectal cancer genetic testing: a prospective outcome trajectories study.

Authors:  Samuel M Y Ho; Judy W C Ho; George A Bonanno; Annie T W Chu; Emily M S Chan
Journal:  BMC Cancer       Date:  2010-06-11       Impact factor: 4.430

10.  Precancerous lesions in colorectal cancer.

Authors:  Fayez Sandouk; Feras Al Jerf; M H D Bassel Al-Halabi
Journal:  Gastroenterol Res Pract       Date:  2013-05-14       Impact factor: 2.260

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