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Evidence that the MCC-APC gene region in 5q21 is not the site for susceptibility to hereditary nonpolyposis colorectal carcinoma.
Peltomäki, P; Sistonen, P; Mecklin, J P; Pylkkänen, L; Aaltonen, L; Nordling, S; Kere, J; Järvinen, H; Hamilton, S R; Petersen, G.
Afiliação
  • Peltomäki P; Department of Medical Genetics, University of Helsinki, Finland.
Cancer Res ; 52(16): 4530-3, 1992 Aug 15.
Article em En | MEDLINE | ID: mdl-1643645
ABSTRACT
Hereditary nonpolyposis colorectal carcinoma (HNPCC) is the most common form of hereditary colon cancer. Autosomal dominant inheritance is evident from pedigrees but the genetic basis of the disorder is otherwise unknown. Recently, two genes in 5q21 involved in colon carcinogenesis, APC and MCC, were identified, and APC was shown to be the gene predisposing to familial adenomatous polyposis. To determine if these genes also confer susceptibility to HNPCC we performed linkage analyses in nine affected families. The MCC-APC region could be formally excluded as the locus for HNPCC in seven families. In one family the results were suggestive of exclusion, although they were not conclusive. The remaining family was uninformative. We used two alternative definitions of affected status. Based on haplotypes for MCC and APC the added pairwise logarithm-of-odds score for all nine families was -22.57 at the recombination fraction of 0.00 using more stringent criteria for the HNPCC phenotype and -22.67 for less stringent criteria. In addition to blood DNA samples from living family members, DNA from formaldehyde-fixed archival pathology specimens from decreased individuals contributed to these linkage results.
Assuntos
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Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 5 / Neoplasias Colorretais / Família / Ligação Genética Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: Cancer Res Ano de publicação: 1992 Tipo de documento: Article País de afiliação: Finlândia
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Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 5 / Neoplasias Colorretais / Família / Ligação Genética Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: Cancer Res Ano de publicação: 1992 Tipo de documento: Article País de afiliação: Finlândia