Detection of numerical chromosome anomalies in interphase cells of benign and malignant thyroid lesions using fluorescence in situ hybridization

Citation
N. Barril et al., Detection of numerical chromosome anomalies in interphase cells of benign and malignant thyroid lesions using fluorescence in situ hybridization, CANC GENET, 117(1), 2000, pp. 50-56
Citations number
35
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
CANCER GENETICS AND CYTOGENETICS
ISSN journal
01654608 → ACNP
Volume
117
Issue
1
Year of publication
2000
Pages
50 - 56
Database
ISI
SICI code
0165-4608(200002)117:1<50:DONCAI>2.0.ZU;2-B
Abstract
Benign and malignant thyroid tumors constitute a wide range of neoplasias s howing recurrent chromosome abnormalities. In an attempt to characterize sp ecific numerical chromosome abnormalities in thyroid tissues, We present he re the findings from a study of archival samples depicted by 10 malignant t umors, 30 benign lesions, and 10 normal thyroid tissues. Fluorescence in si tu hybridization was performed on noncultured samples using biotinylated ce ntromere-specific probes for chromosomes 7, 10, and 17. Trisomy or tetrasom y 7 were present in 19 benign and in 7 malignant tumors. Trisomy 10 or 17 w ere observed in 18 adenomas or goiters and in 9 carcinomas, and monosomy 17 was seen in 2 carcinomas. Our findings suggest that such abnormalities are an in vivo phenomenon and may be important in the neoplastic proliferation of thyroid gland. (C) Elsevier Science Inc., 2000. All rights reserved.