Literature DB >> 20333795

APC gene mutations in Chinese familial adenomatous polyposis patients.

Jian-Qiu Sheng1, Wei-Jia Cui, Lei Fu, Peng Jin, Ying Han, Shu-Jun Li, Ru-Ying Fan, Ai-Qin Li, Ming-Zhi Zhang, Shi-Rong Li.   

Abstract

AIM: To study the characteristics of APC (adenomatous polyposis coli) gene germline mutation in Chinese patients with familial adenomatous polyposis (FAP).
METHODS: APC gene from 14 FAP families was amplified by polymerase chain reaction (PCR) and underwent direct sequencing to determine the micromutation type. For the samples without micromutation, the large fragment deletion of APC gene was examined by multiplex ligation-dependent probe amplification (MLPA).
RESULTS: There were gene micromutations in 9 families with a micromutation detection rate of 64.3% (9/14), including 6 frameshift mutations (66.7%), 1 nonsense mutation (11.1%) and 2 splicing mutations (22.2%). Large fragment deletions were detected by MLPA in 2 families. The total mutation detection rate of micromutations and large fragment deletions was 78.6% (11/14).
CONCLUSION: The detection rate of APC gene germline mutation can be improved by direct sequencing combined with MLPA large fragment deletion detection.

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Year:  2010        PMID: 20333795      PMCID: PMC2846260          DOI: 10.3748/wjg.v16.i12.1522

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


  15 in total

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Authors:  Sara González; Ignacio Blanco; Olga Campos; María Julià; José Reyes; Alfred Llompart; Elena Cabeza; Josep Ramon Germà; Antoni Obrador; Gabriel Capellá
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Review 2.  Correlations between mutation site in APC and phenotype of familial adenomatous polyposis (FAP): a review of the literature.

Authors:  M H Nieuwenhuis; H F A Vasen
Journal:  Crit Rev Oncol Hematol       Date:  2006-10-24       Impact factor: 6.312

3.  A novel coding exon of the human adenomatous polyposis coli gene.

Authors:  Z Suleková; W G Ballhausen
Journal:  Hum Genet       Date:  1995-10       Impact factor: 4.132

4.  Large deletions of the APC gene in 15% of mutation-negative patients with classical polyposis (FAP): a Belgian study.

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Journal:  Hum Mutat       Date:  2005-02       Impact factor: 4.878

5.  Screening for germ-line mutations in familial adenomatous polyposis patients: 61 new patients and a summary of 150 unrelated patients.

Authors:  H Nagase; Y Miyoshi; A Horii; T Aoki; G M Petersen; B Vogelstein; E Maher; M Ogawa; M Maruyama; J Utsunomiya
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6.  Mutational screening of the APC gene in Chilean families with familial adenomatous polyposis: nine novel truncating mutations.

Authors:  Marjorie K De la Fuente; Karin P Alvarez; Alejandro J Letelier; Felipe Bellolio; Mariana L Acuña; Francisca S León; Eliana Pinto; Pilar Carvallo; Francisco López-Köstner
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Review 7.  Genotype-phenotype correlations in 19 Dutch cases with APC gene deletions and a literature review.

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8.  [Detection of adenomatous polyposis coli gene mutations in 31 familial adenomatous polyposis families by using denaturing high performance liquid chromatography].

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Authors:  H F A Vasen; G Möslein; A Alonso; S Aretz; I Bernstein; L Bertario; I Blanco; S Bülow; J Burn; G Capella; C Colas; C Engel; I Frayling; W Friedl; F J Hes; S Hodgson; H Järvinen; J-P Mecklin; P Møller; T Myrhøi; F M Nagengast; Y Parc; R Phillips; S K Clark; M Ponz de Leon; L Renkonen-Sinisalo; J R Sampson; A Stormorken; S Tejpar; H J W Thomas; J Wijnen
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10.  Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects.

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7.  APC Splicing Mutations Leading to In-Frame Exon 12 or Exon 13 Skipping Are Rare Events in FAP Pathogenesis and Define the Clinical Outcome.

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8.  Investigating polymorphisms by bioinformatics is a potential cost-effective method to screen for germline mutations in Chinese familial adenomatous polyposis patients.

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9.  A novel APC mutation identified in a large Chinese family with familial adenomatous polyposis and a brief literature review.

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10.  A novel large germ line deletion in adenomatous polyposis coli (APC) gene associated with familial adenomatous polyposis.

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  10 in total

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