| Literature DB >> 9216715 |
F H Thompson1, R Taetle, J M Trent, Y Liu, K Massey-Brown, K M Scott, R S Weinstein, J C Emerson, D S Alberts, M A Nelson.
Abstract
In a series of 128 karyotyped ovarian carcinomas, 42% of cases with chromosome 1 clonal structural abnormalities had breaks at band 1p36 (usually involving translocations of unknown material). Fluorescent in situ hybridization (FISH) studies using combinations of 1 centromere and 1p36.3-specific probes (16 cases) or 1 centromeric and 17 whole-chromosome paint probes (11 cases with 1p+) revealed a trend toward deletion of 1pter relative to 1 centromere (63%); intratumor heterogeneity; and the origin of 1p+ in 3/11 cases (27%) from chromosome 17 [t(1;17)(p36;?)]. The frequency of this specific breakpoint and its involvement in recurrent translocations suggest that these regions are loci for genes important in the pathogenesis of a subset of sporadic ovarian carcinomas.Entities:
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Year: 1997 PMID: 9216715 DOI: 10.1016/s0165-4608(96)00307-x
Source DB: PubMed Journal: Cancer Genet Cytogenet ISSN: 0165-4608