| Literature DB >> 9134046 |
E Röijer1, R Dahlenfors, J Mark, G Stenman.
Abstract
We report on an adenoid cystic-carcinoma (ACC) with a clonal deletion of 17p as the only karyotypic abnormality. Using different chromosome 17-derived probes we showed by FISH that the deletion encompassed the p53 tumour suppressor gene. Immunohistochemical analysis revealed overexpression of p53 protein in a subpopulation of cells, suggesting a mutation in the remaining p53 allele in these cells. Our findings provide novel information about possible progressional pathways in ACC, and demonstrate the value of combining conventional cytogenetic analysis with-molecular cytogenetic and immunohistochemical methods. This approach is particularly useful in cases with minor cytogenetic abnormalities at the border of visibility.Entities:
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Year: 1997 PMID: 9134046 DOI: 10.1007/bf01092758
Source DB: PubMed Journal: Virchows Arch ISSN: 0945-6317 Impact factor: 4.064