Author/Authors :
Castellvي-Bel، نويسنده , , Sergi and Castells، نويسنده , , Antoni and Strunk، نويسنده , , Mark and Ferrلndez، نويسنده , , ءngel and Piazuelo، نويسنده , , Elena and Milà، نويسنده , , Montserrat and Piٌol، نويسنده , , Virgيnia and Rodrيguez-Moranta، نويسنده , , Francisco Javier Andreu، نويسنده , , Montserrat and Lanas، نويسنده , , ءngel and Piqué، نويسنده , , Josep Maria and The Gastrointestinal Oncology Group of the Spanish Gastroenterological Association، نويسنده ,
Abstract :
Colorectal cancer (CRC) is one of the most common neoplasms and a leading cause of death related to cancer worldwide. Hereditary nonpolyposis colorectal cancer (HNPCC) is the most frequent autosomal dominant predisposition to the development of CRC, accounting for approximately 2.5% of the total CRC burden in Spain. Genomic rearrangements in the MSH2 and MLH1 genes have been reported to account for an important proportion of the mutation spectrum in HNPCC, and DNA dosage techniques have been developed facilitating molecular screening of such deletions/duplications. We screened for MSH2 and MLH1 genomic rearrangements by multiplex ligation-dependent probe amplification (MLPA) in 142 Spanish patients at risk for HNPCC prior to the exon-by-exon mutation scanning and found a deletion encompassing exons 9–16 of MSH2 and a duplication encompassing exons 11–16 of MSH2, both only in one case. These results showed that MSH2/MLH1 rearrangements in Spanish patients at risk for HNPCC seem to be a less frequent mutational event than in other populations.
Keywords :
Colorectal Cancer , HNPCC , Genomic rearrangement , MLH1 , MSH2 , MLPA