Literature DB >> 16168241

Lynch syndrome (hereditary non-polyposis colorectal cancer): current concepts and approaches to management.

Luigi Ricciardiello1, C Richard Boland.   

Abstract

Colorectal cancer is among the most frequent causes of cancer death worldwide. An inherited predisposition to cancer of the colon and other organs, Lynch syndrome-- also called hereditary non-polyposis colorectal cancer--is probably the most frequent cause of hereditary cancer and is often found in a colon cancer patient and traced through other family members. However, this syndrome is not only characterized by the early onset of colon cancers but also by a predisposition to a constellation of extraintestinal cancers that tend to be misdiagnosed. With new diagnostic technologies, the incidence of familial/inherited versus sporadic cases may appear to increase, due to the recognition of cancers in families that do not fulfill clinical guidelines developed prior to knowledge of the genetic basis of this disease. We now have the ability and the responsibility to detect and prevent this disease, and equally important, to direct patients to specifically targeted treatment. Specialists should be aware of the significance of inherited colon cancer and should become familiar with the molecular diagnostic tests now widely available.

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Year:  2005        PMID: 16168241     DOI: 10.1007/s11894-005-0012-2

Source DB:  PubMed          Journal:  Curr Gastroenterol Rep        ISSN: 1522-8037


  90 in total

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Authors:  R Ward; A Meagher; I Tomlinson; T O'Connor; M Norrie; R Wu; N Hawkins
Journal:  Gut       Date:  2001-06       Impact factor: 23.059

2.  A polymorphism in the ATM gene modulates the penetrance of hereditary non-polyposis colorectal cancer.

Authors:  P Maillet; P O Chappuis; G Vaudan; Z Dobbie; H Müller; P Hutter; A P Sappino
Journal:  Int J Cancer       Date:  2000-12-15       Impact factor: 7.396

3.  A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome.

Authors:  E Mangold; C Pagenstecher; M Leister; M Mathiak; A Rütten; W Friedl; P Propping; T Ruzicka; R Kruse
Journal:  J Med Genet       Date:  2004-07       Impact factor: 6.318

4.  MSH2 genomic deletions are a frequent cause of HNPCC.

Authors:  J Wijnen; H van der Klift; H Vasen; P M Khan; F Menko; C Tops; H Meijers Heijboer; D Lindhout; P Møller; R Fodde
Journal:  Nat Genet       Date:  1998-12       Impact factor: 38.330

5.  Interpretation of genetic test results for hereditary nonpolyposis colorectal cancer: implications for clinical predisposition testing.

Authors:  S Syngal; E A Fox; C Li; M Dovidio; C Eng; R D Kolodner; J E Garber
Journal:  JAMA       Date:  1999-07-21       Impact factor: 56.272

6.  Histopathology of colorectal carcinomas and adenomas in cancer family syndrome.

Authors:  J P Mecklin; P Sipponen; H J Järvinen
Journal:  Dis Colon Rectum       Date:  1986-12       Impact factor: 4.585

7.  Effects of cyclin D1 polymorphism on age of onset of hereditary nonpolyposis colorectal cancer.

Authors:  S Kong; C I Amos; R Luthra; P M Lynch; B Levin; M L Frazier
Journal:  Cancer Res       Date:  2000-01-15       Impact factor: 12.701

8.  CYCLIN D1 as a genetic modifier in hereditary nonpolyposis colorectal cancer.

Authors:  S Bala; P Peltomäki
Journal:  Cancer Res       Date:  2001-08-15       Impact factor: 12.701

9.  Somatic frameshift mutations in the BAX gene in colon cancers of the microsatellite mutator phenotype.

Authors:  N Rampino; H Yamamoto; Y Ionov; Y Li; H Sawai; J C Reed; M Perucho
Journal:  Science       Date:  1997-02-14       Impact factor: 47.728

10.  Evaluation of microsatellite instability and immunohistochemistry for the prediction of germ-line MSH2 and MLH1 mutations in hereditary nonpolyposis colon cancer families.

Authors:  Siobhan S Wahlberg; James Schmeits; George Thomas; Massimo Loda; Judy Garber; Sapna Syngal; Richard D Kolodner; Edward Fox
Journal:  Cancer Res       Date:  2002-06-15       Impact factor: 12.701

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  5 in total

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Authors:  Heiying Jin; Xuanzhong Tan; Xiufang Liu; Yijiang Ding
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2.  Analysis of mismatch repair gene mutations in Turkish HNPCC patients.

Authors:  Berrin Tunca; Monica Pedroni; Gulsah Cecener; Unal Egeli; Enrica Borsi; Abdullah Zorluoglu; Carmela Di Gregorio; Tuncay Yilmazlar; Omer Yerci; Maurizio Ponz de Leon
Journal:  Fam Cancer       Date:  2010-09       Impact factor: 2.375

3.  Mismatch repair protein expression and colorectal cancer in Hispanics from Puerto Rico.

Authors:  Wilfredo E De Jesus-Monge; Carmen Gonzalez-Keelan; Ronghua Zhao; Stanley R Hamilton; Miguel Rodriguez-Bigas; Marcia Cruz-Correa
Journal:  Fam Cancer       Date:  2010-06       Impact factor: 2.375

4.  Investigation on the role of nsSNPs in HNPCC genes--a bioinformatics approach.

Authors:  C George Priya Doss; Rao Sethumadhavan
Journal:  J Biomed Sci       Date:  2009-04-24       Impact factor: 8.410

5.  Detection of mismatch repair gene germline mutation carrier among Chinese population with colorectal cancer.

Authors:  Hei-Ying Jin; Xiufang Liu; Vicky Ka Ming Li; Yijiang Ding; Bolin Yang; Jianxiang Geng; Rensheng Lai; Shuqing Ding; Min Ni; Ronghua Zhao
Journal:  BMC Cancer       Date:  2008-02-07       Impact factor: 4.430

  5 in total

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