INSTABILITY OF CHROMOSOME-1, CHROMOSOME-3, CHROMOSOME-16, AND CHROMOSOME-17 IN PRIMARY BREAST CARCINOMAS INFERRED BY FLUORESCENCE IN-SITU HYBRIDIZATION

Citation
K. Anamthawatjonsson et al., INSTABILITY OF CHROMOSOME-1, CHROMOSOME-3, CHROMOSOME-16, AND CHROMOSOME-17 IN PRIMARY BREAST CARCINOMAS INFERRED BY FLUORESCENCE IN-SITU HYBRIDIZATION, Cancer genetics and cytogenetics, 88(1), 1996, pp. 1-7
Citations number
20
Categorie Soggetti
Oncology,"Genetics & Heredity
ISSN journal
01654608
Volume
88
Issue
1
Year of publication
1996
Pages
1 - 7
Database
ISI
SICI code
0165-4608(1996)88:1<1:IOCCCA>2.0.ZU;2-5
Abstract
Abnormalities of chromosomes 1, 3, 16, and 17 were examined in 203 met aphase cells from 12 cases of primary breast carcinoma using fluoresce nce in situ hybridization with chromosome painting probes. The most co mmon structural abnormalities were chromosomal rearrangements, especia lly translocations, and chromosome 17 was most frequently involved in these types of changes. Chromosome 16 was preferentially involved in t he losses and deletions, while chromosomes 1 and 17 were more involved in the gains, including amplifications, than other chromosomes. This approach has revealed a different profile of abnormalities from those normally shown by G-banding analysis. Some of these changes are likely to be novel and may be of biologic or clinical importance in breast c ancer.