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[Detection mutations in the DNA mismatch repair genes of hMLH1 and hMSH2 genes in Colombian families with suspicion of hereditary non-polyposis colorectal carcinoma (Lynch syndrome)]. / Detección de mutaciones de los genes hMLH1 y hMSH2 del sistema de reparación de malos apareamientos del ADN en familias colombianas sospechosas de cancer colorrectal no polipósico hereditario (síndrome de Lynch).
Gómez, Andrea; Salguero, Gustavo; García, Herbert; Aristizábal, Fabio; Gutiérrez, Oscar; Angel, Luis Alberto; Padrón, Jorge; Martínez, Carlos; Martínez, Humberto; Malaver, Omar; Barvo, Rosa; Giraldo, Alejandro.
Afiliação
  • Gómez A; Facultad de Medicina e Instituto de Genética, Universidad Nacional de Colombia, Bogotá, D. C., Colombia.
Biomedica ; 25(3): 315-24, 2005 Sep.
Article em Es | MEDLINE | ID: mdl-16276679
ABSTRACT

INTRODUCTION:

Colorectal cancer (CRC) is the second highest cause of cancer mortality in developed countries. In Colombia, CRC ranks fifth as a cause of cancer death. Approximately 75% of CRC appear to be spontaneous and 25% are familial, with 5% of the latter clearly hereditary. Of these, hereditary non-polyposis colorectal carcinoma (HNPCC)-or Lynch syndrome is the most important.

OBJECTIVE:

Herein, the two most important genes involved in Lynch syndrome, the hMLH1 and hMSH2 were analyzed for presence of mutations. MATERIALS AND

METHODS:

Seventeen Colombian families that fulfilled the Amsterdam II criteria or Bethesda guidelines for Lynch syndrome were selected. The of 35 exons of hMLH1 and hMSH2 genes were screened by SSCP and those with electrophoretic variants were sequenced.

RESULTS:

Eight germinal mutations were detected, corresponding to a 47% detection mutation rate. Six of the eight mutations have previously been reported. These consisted of the following mutations a single base substitution at the donor splicing site of exon 9, a single base substitution (A>G) at codon 755 of the exon 17, and another single base substitution (G>A) at codon 681 of exon 18. The two novel mutations consisted of a single base substitution (C>T) at codon 640 of exon 17 of the hMLH1 gene and a two-nucleotide deletion (TG) at codon 184 of exon 3 of hMSH2 gene. In addition, two families were observed with a polymorphism in the intron 13 (G>A) nt 1558+14, of hMLH1 gene.

CONCLUSIONS:

This study represented the first survey for detecting mutations associated with Lynch syndrome in Colombia, and is intended to lead to the establishment of a management and prevention program.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Nucleares / Proteínas de Transporte / Neoplasias Colorretais Hereditárias sem Polipose / Pareamento Incorreto de Bases / Reparo do DNA / Proteína 2 Homóloga a MutS Tipo de estudo: Diagnostic_studies / Qualitative_research Limite: Adolescent / Adult / Female / Humans / Male / Middle aged País/Região como assunto: America do sul / Colombia Idioma: Es Revista: Biomedica Ano de publicação: 2005 Tipo de documento: Article País de afiliação: Colômbia
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Nucleares / Proteínas de Transporte / Neoplasias Colorretais Hereditárias sem Polipose / Pareamento Incorreto de Bases / Reparo do DNA / Proteína 2 Homóloga a MutS Tipo de estudo: Diagnostic_studies / Qualitative_research Limite: Adolescent / Adult / Female / Humans / Male / Middle aged País/Região como assunto: America do sul / Colombia Idioma: Es Revista: Biomedica Ano de publicação: 2005 Tipo de documento: Article País de afiliação: Colômbia