Cytogenetic findings in 31 papillary thyroid carcinomas.

Autor: Roque L; Department of Morphological Pathology Portuguese Institute for Oncology, Lisbon., Clode AL, Gomes P, Rosa-Santos J, Soares J, Castedo S
Jazyk: angličtina
Zdroj: Genes, chromosomes & cancer [Genes Chromosomes Cancer] 1995 Jul; Vol. 13 (3), pp. 157-62.
DOI: 10.1002/gcc.2870130304
Abstrakt: Chromosome studies performed on 31 papillary thyroid carcinomas (PTCs) revealed clonal numerical and structural abnormalities in 12 tumors. The numerical clonal aberrations found were trisomy 2, trisomy 7, and loss of the Y chromosome. A nonrandom telomeric association, tas(15;16)(p13;p13), was observed in one carcinoma. Structural alterations with a breakpoint at 10q11.2 were detected in two tumors. Other chromosomes involved in rearrangements were chromosomes 1, 2, 3, 5, 7, 9, 11, 12, and 14. The observation of clonal changes of chromosome 2 [i(2)(q10) and trisomy 2] in two tumors, which were both histologically classified as tall-cell PTC variants, suggests that gain of 2q may be important in the development of this morphological variant.
Databáze: MEDLINE