Institut de Recherche sur le Cancer de Lille (IRCL), Centre JP Aubert, Unité Inserm 837, Lille, France.
Leuk Res. 2011 Apr;35(4):448-58. doi: 10.1016/j.leukres.2010.07.012. Epub 2010 Aug 3.
To ascertain genomic alterations associated with Imatinib resistance in chronic myeloid leukaemia, we performed high resolution genomic analysis of CD34(+) cells from 25 Imatinib (IM) resistant and 11 responders CML patients. Using patients' T-cells as reference, we found significant association between number of acquired cryptic copy number alterations (CNA) and disease phase (p=0.036) or loss of IM response for patients diagnosed in chronic phase (CP) (p=0.04). Recurrent cryptic losses were identified on chromosomes 7, 12 and 13. On chromosome 7, recurrent deletions of the IKZF1 locus were detected, for the first time, in 4 patients in CP.
为了确定与慢性髓性白血病伊马替尼耐药相关的基因组改变,我们对 25 例伊马替尼(IM)耐药和 11 例缓解的 CML 患者的 CD34(+)细胞进行了高分辨率基因组分析。使用患者的 T 细胞作为参考,我们发现获得性隐匿拷贝数改变(CNA)的数量与疾病阶段(p=0.036)或慢性期(CP)诊断患者的 IM 反应丧失之间存在显著关联(p=0.04)。在染色体 7、12 和 13 上发现了复发性隐匿性缺失。在 CP 的 4 例患者中,首次检测到 IKZF1 基因座的反复缺失。