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Comparison of cytogenetic changes between primary and relapsed patients with borderline tumors of the ovary.

机译:比较原发性和复发性卵巢交界性肿瘤患者的细胞遗传学变化。

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摘要

The aim of this work was to compare cytogenetic changes in primary and relapsed borderline tumors of the ovary. We analyzed 11 tumors (6 primary and 5 relapsed) by conventional GTG banding analysis and fluorescence in situ hybridization. The tumors studied were clinical stages I and III. Genomic imbalances were detected in both investigated groups. In the primary tumors group, only simple chromosome changes were detected. There were gains of chromosome 12, 7, and 8. The presence of additional copies of chromosomes 12 and 7 was independent of histologic subtype, whereas trisomy 8 appeared only in serous tumors. In the group of relapsed borderline tumors, besides trisomies 7 and 12, the structural aberrations of chromosomes 1, 6q, 7q, and 10q were revealed. Gains of tested oncogenes (CCND1 and MYC) have been demonstrated in both groups of investigated tumors. Gains of CCNC1 and MYC genes could be of prognostic value in borderline tumors, but this assumption requires further research.
机译:这项工作的目的是比较卵巢原发性和复发性交界性肿瘤的细胞遗传学变化。我们通过常规GTG谱带分析和荧光原位杂交分析了11种肿瘤(6例原发性和5例复发)。研究的肿瘤是I和III期临床。在两个研究组中均检测到基因组失衡。在原发性肿瘤组中,仅检测到简单的染色体变化。获得了第12、7和8号染色体。存在额外的第12和7号染色体拷贝与组织学亚型无关,而8三体性仅出现在浆液性肿瘤中。在复发的交界性肿瘤中,除了三体性7和12外,还发现了染色体1、6q,7q和10q的结构畸变。在两组研究的肿瘤中均证实了受试癌基因(CCND1和MYC)的增加。 CCNC1和MYC基因的获得可能在边缘性肿瘤中具有预后价值,但这一假设需要进一步研究。

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