Detection of numerical chromosomal aberrations in oral leukoplakias and HNSCC by fluorescence in situ hybridization

Citation
C. Lenz et al., Detection of numerical chromosomal aberrations in oral leukoplakias and HNSCC by fluorescence in situ hybridization, HNO, 48(5), 2000, pp. 367-371
Citations number
18
Categorie Soggetti
Otolaryngology
Journal title
HNO
ISSN journal
00176192 → ACNP
Volume
48
Issue
5
Year of publication
2000
Pages
367 - 371
Database
ISI
SICI code
0017-6192(200005)48:5<367:DONCAI>2.0.ZU;2-D
Abstract
The tumorigenesis of head and neck squamous cell carcinoma (HNSCC) has been proposed to represent a multistep process characterized by an accumulation of genetic alterations. To study numerical chromosomal aberrations and chr omosomal imbalances, biopsies of 11 malignant tumours and biopsies of 16 or al premalignant lesions (leukoplakias) were analyzed by fluorescence in sit u hybridization (FISH) using centromeric probes for chromosomes 1,7,9, 10 a nd 17. The comparison of the alterations observed in simple leukoplakias (g roup 1,n=8), dysplastic leukoplakias (group 2, n=8) and malignant tumours ( group 3,n=11) by the Cochran-Armitage Trend Test revealed an increasing num ber of numerical chromosomal abberations. This difference was statistically highly significant (P<0,001). The data open up the possibility that FISH a nalysis might help to better characterize the progression of premalignant o ral leukoplakias.