Department of Hemato-Oncology, University Hospital Olomouc, Czech Republic.
Leuk Lymphoma. 2010 Feb;51(2):304-13. doi: 10.3109/10428190903518311.
Array-based comparative genomic hybridization (arrayCGH) studies in chronic lymphocytic leukemia (CLL) have revealed novel recurrent chromosomal imbalances, such as a gain of chromosome 2p. However, a detailed cytogenetic analysis of the 2p gain region has not been elucidated. Here, we present cytogenetic and molecular cytogenetic analysis of 16 such cases selected from a group of 200 patients with CLL based on CGH and/or arrayCGH data. We revealed significant heterogeneity of the region of gain on 2p in CLL, including a new recurrent aberration: the dicentric chromosome, dic(2;18). In our cases, the region of gain involved three genes (MYCN, REL, and ALK) and was associated with an unmutated IgVH status in 14 out of 16 cases. We consider this aberration clinically important in CLL and suggest that an examination of the gene(s) located in region of gain should be included in the routine fluorescence in situ hybridization screening method used for patients with CLL.
基于阵列的比较基因组杂交 (arrayCGH) 研究在慢性淋巴细胞白血病 (CLL) 中揭示了新的染色体不平衡,例如染色体 2p 的获得。然而,2p 增益区域的详细细胞遗传学分析尚未阐明。在这里,我们根据 CGH 和/或 arrayCGH 数据,从 200 例 CLL 患者中选择了 16 例进行细胞遗传学和分子细胞遗传学分析。我们揭示了 CLL 中 2p 增益区域的显著异质性,包括一种新的重现性畸变:双着丝粒染色体,dic(2;18)。在我们的病例中,增益区域涉及三个基因(MYCN、REL 和 ALK),并且在 16 例中的 14 例中与未突变的 IgVH 状态相关。我们认为这种畸变在 CLL 中具有临床重要性,并建议在用于 CLL 患者的常规荧光原位杂交筛选方法中应包括位于增益区域的基因的检查。