Roque L, Clode A L, Gomes P, Rosa-Santos J, Soares J, Castedo S
Department of Morphological Pathology Portuguese Institute for Oncology, Lisbon.
Genes Chromosomes Cancer. 1995 Jul;13(3):157-62. doi: 10.1002/gcc.2870130304.
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.
对31例甲状腺乳头状癌(PTC)进行的染色体研究显示,12例肿瘤存在克隆性数目和结构异常。发现的数目克隆畸变包括三体2、三体7和Y染色体缺失。在1例癌中观察到非随机的端粒关联,tas(15;16)(p13;p13)。在2例肿瘤中检测到在10q11.2处有断点的结构改变。参与重排的其他染色体有1、2、3、5、7、9、11、12和14号染色体。在2例均组织学分类为高细胞PTC变体的肿瘤中观察到染色体2的克隆变化[i(2)(q10)和三体2],这表明2q的增加可能在这种形态学变体的发生中起重要作用。