GENOMIC HETEROGENEITY IN BLADDER-CANCER AS DETECTED BY FLUORESCENCE IN-SITU HYBRIDIZATION

Citation
H. Yokogi et al., GENOMIC HETEROGENEITY IN BLADDER-CANCER AS DETECTED BY FLUORESCENCE IN-SITU HYBRIDIZATION, British Journal of Urology, 78(5), 1996, pp. 699-703
Citations number
15
Categorie Soggetti
Urology & Nephrology
Journal title
ISSN journal
00071331
Volume
78
Issue
5
Year of publication
1996
Pages
699 - 703
Database
ISI
SICI code
0007-1331(1996)78:5<699:GHIBAD>2.0.ZU;2-Q
Abstract
Objective To investigate the relationship between genomic heterogeneit y and tumour grade, stage and DNA content in 30 transitional cell carc inomas (TCCs) of the urinary bladder. Materials and methods Tissue spe cimens from 30 patients (25 men and five women) with newly diagnosed T CC of the urinary bladder were examined for genomic heterogeneity usin g fluorescence in situ hybridization (FISH) with chromosome-specific D NA probes; the copy number of pericentromeric sequences on chromosomes 7, 9 and 17 was detected within interphase nuclei in contact preparat ions from the tumour specimens. Results The aneusomy of chromosomes 7, 9 and 17 was significantly higher in aneuploid than in diploid tumour s (P < 0.001). Tumour grade and stage were strongly associated with an eusomy for chromosome 17 (P < 0.01, P < 0.001, respectively). The aneu somy of chromosomes 7 and 9 were significantly correlated with increas ing tumour stage (P < 0.001), but not with tumour grade. Conclusion Th ese results suggest that the measurement of aneusomy using FISH, espec ially for chromosome 17, in bladder cancer may offer a new objective a nd quantitative assay of the biological potential of individual tumour s.