Literature DB >> 23399955

Prevalence of germline PTEN, BMPR1A, SMAD4, STK11, and ENG mutations in patients with moderate-load colorectal polyps.

Joanne Ngeow1, Brandie Heald, Lisa A Rybicki, Mohammed S Orloff, Jin Lian Chen, Xiuli Liu, Lisa Yerian, Joseph Willis, Heli J Lehtonen, Rainer Lehtonen, Jessica L Mester, Jessica Moline, Carol A Burke, James Church, Lauri A Aaltonen, Charis Eng.   

Abstract

BACKGROUND & AIMS: Gastrointestinal polyposis is a common clinical problem, yet there is no consensus on how to best manage patients with moderate-load polyposis. Identifying genetic features of this disorder could improve management and especially surveillance of these patients. We sought to determine the prevalence of hamartomatous polyposis-associated mutations in the susceptibility genes PTEN, BMPR1A, SMAD4, ENG, and STK11 in individuals with ≥5 gastrointestinal polyps, including at least 1 hamartomatous or hyperplastic/serrated polyp.
METHODS: We performed a prospective, referral-based study of 603 patients (median age: 51 years; range, 2-89 years) enrolled from June 2006 through January 2012. Genomic DNA was extracted from peripheral lymphocytes and analyzed for specific mutations and large rearrangements in PTEN, BMPR1A, SMAD4, and STK11, as well as mutations in ENG. Recursive partitioning analysis was used to determine cutoffs for continuous variables. The prevalence of mutations was compared using Fisher's exact test. Logistic regression analyses were used to determine univariate and multivariate risk factors.
RESULTS: Of 603 patients, 119 (20%) had a personal history of colorectal cancer and most (n = 461 [76%]) had <30 polyps. Seventy-seven patients (13%) were found to have polyposis-associated mutations, including 11 in ENG (1.8%), 13 in PTEN (2.2%), 13 in STK11 (2.2%), 20 in BMPR1A (3.3%), and 21 in SMAD4 (3.5%). Univariate clinical predictors for risk of having these mutations included age at presentation younger than 40 years (19% vs 10%; P = .008), a polyp burden of ≥30 (19% vs 11%; P = .014), and male sex (16% vs 10%; P = .03). Patients who had ≥1 ganglioneuroma (29% vs 2%; P < .001) or presented with polyps of ≥3 histologic types (20% vs 2%; P = .003) were more likely to have germline mutations in PTEN.
CONCLUSIONS: Age younger than 40 years, male sex, and specific polyp histologies are significantly associated with risk of germline mutations in hamartomatous-polyposis associated genes. These associations could guide clinical decision making and further investigations.
Copyright © 2013 AGA Institute. Published by Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23399955      PMCID: PMC3969031          DOI: 10.1053/j.gastro.2013.02.001

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  37 in total

1.  ENG mutations in MADH4/BMPR1A mutation negative patients with juvenile polyposis.

Authors:  J R Howe; J L Haidle; G Lal; J Bair; C Song; B Pechman; S Chinnathambi; H T Lynch
Journal:  Clin Genet       Date:  2007-01       Impact factor: 4.438

Review 2.  Gastrointestinal polyposes: clinical, pathological and molecular features.

Authors:  Jeremy R Jass
Journal:  Gastroenterol Clin North Am       Date:  2007-12       Impact factor: 3.806

3.  A population-based study of colorectal cancer histology in the United States, 1998-2001.

Authors:  Sherri L Stewart; Jennifer M Wike; Ikuko Kato; Denise R Lewis; Frances Michaud
Journal:  Cancer       Date:  2006-09-01       Impact factor: 6.860

4.  SMAD genes in juvenile polyposis.

Authors:  S Roth; P Sistonen; R Salovaara; A Hemminki; A Loukola; M Johansson; E Avizienyte; K A Cleary; P Lynch; C I Amos; P Kristo; J P Mecklin; I Kellokumpu; H Järvinen; L A Aaltonen
Journal:  Genes Chromosomes Cancer       Date:  1999-09       Impact factor: 5.006

5.  Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis.

Authors:  Kevin Sweet; Joseph Willis; Xiao-Ping Zhou; Carol Gallione; Takeshi Sawada; Pia Alhopuro; Sok Kean Khoo; Attila Patocs; Cossette Martin; Scott Bridgeman; John Heinz; Robert Pilarski; Rainer Lehtonen; Thomas W Prior; Thierry Frebourg; Bin Tean Teh; Douglas A Marchuk; Lauri A Aaltonen; Charis Eng
Journal:  JAMA       Date:  2005-11-16       Impact factor: 56.272

6.  Suspected hereditary nonpolyposis colorectal cancer: International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC) criteria and results of genetic diagnosis.

Authors:  J G Park; H F Vasen; K J Park; P Peltomaki; M Ponz de Leon; M A Rodriguez-Bigas; J Lubinski; N E Beck; M L Bisgaard; M Miyaki; J T Wijnen; S Baba; H T Lynch
Journal:  Dis Colon Rectum       Date:  1999-06       Impact factor: 4.585

7.  Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis.

Authors:  M Nielsen; F J Hes; F M Nagengast; M M Weiss; E M Mathus-Vliegen; H Morreau; M H Breuning; J T Wijnen; C M J Tops; H F A Vasen
Journal:  Clin Genet       Date:  2007-05       Impact factor: 4.438

8.  American founder mutation for attenuated familial adenomatous polyposis.

Authors:  Deborah W Neklason; Jeffery Stevens; Kenneth M Boucher; Richard A Kerber; Nori Matsunami; Jahn Barlow; Geraldine Mineau; Mark F Leppert; Randall W Burt
Journal:  Clin Gastroenterol Hepatol       Date:  2007-12-11       Impact factor: 11.382

Review 9.  Hamartomatous polyposis syndromes.

Authors:  Amanda Gammon; Kory Jasperson; Wendy Kohlmann; Randall W Burt
Journal:  Best Pract Res Clin Gastroenterol       Date:  2009       Impact factor: 3.043

10.  Cowden syndrome-affected patients with PTEN promoter mutations demonstrate abnormal protein translation.

Authors:  Rosemary E Teresi; Kevin M Zbuk; Marcus G Pezzolesi; Kristin A Waite; Charis Eng
Journal:  Am J Hum Genet       Date:  2007-08-15       Impact factor: 11.025

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  10 in total

Review 1.  Genetic architecture of colorectal cancer.

Authors:  Ulrike Peters; Stephanie Bien; Niha Zubair
Journal:  Gut       Date:  2015-07-17       Impact factor: 23.059

Review 2.  Genetic Testing for Polyposis Syndromes.

Authors:  Khateriaa Pyrtel
Journal:  Clin Colon Rectal Surg       Date:  2016-12

3.  Next-Generation Sequencing Panels for the Diagnosis of Colorectal Cancer and Polyposis Syndromes: A Cost-Effectiveness Analysis.

Authors:  Carlos J Gallego; Brian H Shirts; Caroline S Bennette; Greg Guzauskas; Laura M Amendola; Martha Horike-Pyne; Fuki M Hisama; Colin C Pritchard; William M Grady; Wylie Burke; Gail P Jarvik; David L Veenstra
Journal:  J Clin Oncol       Date:  2015-05-04       Impact factor: 44.544

4.  WWP1 Gain-of-Function Inactivation of PTEN in Cancer Predisposition.

Authors:  Yu-Ru Lee; Lamis Yehia; Takahiro Kishikawa; Ying Ni; Brandie Leach; Jinfang Zhang; Nivedita Panch; Jing Liu; Wenyi Wei; Charis Eng; Pier Paolo Pandolfi
Journal:  N Engl J Med       Date:  2020-05-28       Impact factor: 91.245

5.  Attenuated polyposis of the large bowel: a morphologic and molecular approach.

Authors:  Maurizio Ponz de Leon; Monica Pedroni; Luca Roncucci; Federica Domati; Giuseppina Rossi; Giulia Magnani; Annalisa Pezzi; Rossella Fante; Luca Reggiani Bonetti
Journal:  Fam Cancer       Date:  2017-04       Impact factor: 2.375

6.  Early-onset renal cell carcinoma in PTEN harmatoma tumour syndrome.

Authors:  Raymond H Kim; Xiangling Wang; Andrew J Evans; Steven C Campbell; Jane K Nguyen; Kirsten M Farncombe; Charis Eng
Journal:  NPJ Genom Med       Date:  2020-09-29       Impact factor: 8.617

Review 7.  New genes emerging for colorectal cancer predisposition.

Authors:  Clara Esteban-Jurado; Pilar Garre; Maria Vila; Juan José Lozano; Anna Pristoupilova; Sergi Beltrán; Anna Abulí; Jenifer Muñoz; Francesc Balaguer; Teresa Ocaña; Antoni Castells; Josep M Piqué; Angel Carracedo; Clara Ruiz-Ponte; Xavier Bessa; Montserrat Andreu; Luis Bujanda; Trinidad Caldés; Sergi Castellví-Bel
Journal:  World J Gastroenterol       Date:  2014-02-28       Impact factor: 5.742

8.  Syndromic and sporadic inflammatory/hyperplastic small-bowel polyps: a comparative study.

Authors:  Xiuli Liu; Derrick Chen; Mohannad Dugum; Bela Horvath; Lisi Yuan; Shu-Yuan Xiao
Journal:  Gastroenterol Rep (Oxf)       Date:  2015-06-06

Review 9.  Genetic basis of Cowden syndrome and its implications for clinical practice and risk management.

Authors:  Amanda Gammon; Kory Jasperson; Marjan Champine
Journal:  Appl Clin Genet       Date:  2016-07-13

10.  Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer.

Authors:  Clara Esteban-Jurado; Maria Vila-Casadesús; Pilar Garre; Juan José Lozano; Anna Pristoupilova; Sergi Beltran; Jenifer Muñoz; Teresa Ocaña; Francesc Balaguer; Maria López-Cerón; Miriam Cuatrecasas; Sebastià Franch-Expósito; Josep M Piqué; Antoni Castells; Angel Carracedo; Clara Ruiz-Ponte; Anna Abulí; Xavier Bessa; Montserrat Andreu; Luis Bujanda; Trinidad Caldés; Sergi Castellví-Bel
Journal:  Genet Med       Date:  2014-07-24       Impact factor: 8.822

  10 in total

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