Evidence map›Paper›PMID 19531215›Full record

ArticleBMC medical genetics2009

Molecular analysis of the APC and MUTYH genes in Galician and Catalonian FAP families: a different spectrum of mutations?

Nuria Gómez-Fernández, Sergi Castellví-Bel, Ceres Fernández-Rozadilla, Francesc Balaguer, Jenifer Muñoz, Irene Madrigal, Montserrat Milà, Begoña Graña, Ana Vega, Antoni Castells and 2 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC medical genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.8field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  9. Tumor suppressor genes in familial adenomatous polyposis.Gastroenterology and hepatology from bed to bench · 2017
    Review
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

12 authors at 7 institutions in 1 country.

Nuria Gómez-FernándezFundación Pública Galega de Medicina Xenómica, Grupo de Medicina Xenómica-USC, CIBERER, Santiago de Compostela, Galicia, Spain. nuria.gomez@usc.es
Sergi Castellví-Bel
Ceres Fernández-Rozadilla
Francesc Balaguer
Jenifer Muñoz
Irene Madrigal
Montserrat Milà
Begoña Graña
Ana Vega
Antoni Castells
Angel Carracedo
Clara Ruiz-Ponte
Fundación Pública Galega de Medicina Xenómica · ESHospital Clínic de Barcelona · ESCentre for Biomedical Network Research on Rare Diseases · ESConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESHospital Provincial de Conxo · ESServicio Gallego de Salud · ESUniversitat de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFamilial adenomatous polyposis (FAP) is an autosomal dominant-inherited colorectal cancer syndrome, caused by germline mutations in the APC gene. Recently, biallelic mutations in MUTYH have also been identified in patients with multiple colorectal adenomas and in APC-negative patients with FAP. The aim of this work is therefore to determine the frequency of APC and MUTYH mutations among FAP families from two Spanish populations.

methodsEighty-two unrelated patients with classical or attenuated FAP were screened for APC germline mutations. MUTYH analysis was then conducted in those APC-negative families and in 9 additional patients from a previous study. Direct sequencing, SSCP analysis and TaqMan genotyping were used to identify point and frameshift mutations, meanwhile large rearrangements in the APC gene were screened by multiplex ligation-dependent probe amplification (MLPA).

resultsAPC germline mutations were found in 39% of the patients and, despite the great number of genetic variants described so far in this gene, seven new mutations were identified. The two hotspots at codons 1061 and 1309 of the APC gene accounted for 9,4% of the APC-positive families, although they were underrepresented in Galician samples. The deletion at codon 1061 was not found in 19 APC-positive Galician patients but represented 23% of the Catalonian positive families (p = 0,058). The same trend was observed at codon 1309, even though statistical analysis showed no significance between populations. Twenty-four percent of the APC-negative patients carried biallelic MUTYH germline mutations, and showed an attenuated polyposis phenotype generally without extracolonic manifestations. New genetic variants were found, as well as the two hotspots already reported (p.Tyr165Cys and p.Gly382Asp).

conclusionThe results we present indicate that in Galician patients the frequency of the hotspot at codon 1061 in APC differs significantly from the Catalonian and also other Caucasian populations. Similar results had already been obtained in a previous study and could be due to the genetic isolation of the Galician population. MUTYH analysis is also recommended for all APC-negative families, even if a recessive inheritance is not confirmed.

Indexed as

Genes, APCGerm-Line MutationAdenomatous Polyposis ColiAdolescentAdultDNA GlycosylasesEthnicityFemaleGene FrequencyHumansIn Situ Hybridization, FluorescenceMaleMiddle AgedNucleic Acid Amplification TechniquesSequence Analysis, DNASequence DeletionDNA GlycosylasesmutY adenine glycosylase

Identifiers

PMID19531215
PMCPMC2702373
OpenAlexW2066845288

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.