Laboratory of Mutagenesis, Federal State Budgetary Institution, Research Centre for Medical Genetics, Moskvorechie str., 1, Moscow, Russian Federation, 115522.
Department of Molecular and Cellular Genetics, State Budgetary Educational Institution of Higher Professional Education "Russian National Research Medical University named after N.I. Pirogov" of Ministry of Health of the Russian Federation, Ostrovityanova str., 1, Moscow, Russian Federation, 117997.
BMC Med Genomics. 2019 Mar 13;12(Suppl 2):37. doi: 10.1186/s12920-019-0481-z.
Approximately 5-20% of chronic myeloid leukemia (CML) patients demonstrate primary resistance or intolerance to imatinib. None of the existing predictive scores gives a good prognosis of TKI efficacy. Gene polymorphisms, expression and microRNAs are known to be involved in the pathogenesis of TKI resistance in CML. The aim of our study is to find new molecular markers of TKI therapy efficacy in CML patients.
Newly diagnosed patients with Ph+ CML in chronic phase were included in this study. Optimal and non-optimal responses to TKI were estimated according to ELN 2013 recommendation. We performed genotyping of selected polymorphisms in 62 blood samples of CML patients, expression profiling of 33 RNA samples extracted from blood and miRNA profiling of 800 miRNA in 12 blood samples of CML patients.
The frequencies of genotypes at the studied loci did not differ between groups of patients with an optimal and non-optimal response to TKI therapy. Analysis of the expression of 34,681 genes revealed 26 differently expressed genes (p < 0.05) in groups of patients with different TKI responses, but differences were very small and were not confirmed by qPCR. Finally, we did not find difference in miRNA expression between the groups.
Using modern high-throughput methods such as whole-exome sequencing, transcriptome and miRNA analysis, we could not find reliable molecular markers for early prediction of TKI efficiency in Ph+ CML patients.
约 5-20%的慢性髓性白血病 (CML) 患者对伊马替尼表现出原发性耐药或不耐受。现有的预测评分都不能很好地预测 TKI 的疗效。基因多态性、表达和 microRNAs 已知参与 CML 中 TKI 耐药的发病机制。我们研究的目的是寻找 CML 患者 TKI 治疗疗效的新分子标志物。
本研究纳入了新诊断的 Ph+ CML 慢性期患者。根据 ELN 2013 建议,评估 TKI 的最佳和非最佳反应。我们对 62 份 CML 患者血液样本进行了选定多态性的基因分型,对 33 份来自血液的 RNA 样本进行了表达谱分析,对 12 份 CML 患者的 800 个 miRNA 进行了 miRNA 谱分析。
在对 TKI 治疗有最佳和非最佳反应的患者组中,研究位点的基因型频率没有差异。对 34681 个基因的表达分析显示,在不同 TKI 反应的患者组中有 26 个差异表达基因(p<0.05),但差异非常小,且未通过 qPCR 得到证实。最后,我们没有发现两组间 miRNA 表达的差异。
使用全外显子组测序、转录组和 miRNA 分析等现代高通量方法,我们无法找到可靠的分子标志物,用于早期预测 Ph+ CML 患者 TKI 的疗效。