Division of Hematology.
Blood. 2014 Apr 10;123(15):2412-5. doi: 10.1182/blood-2013-10-532374. Epub 2014 Mar 4.
Nucleophosmin-mutated acute myeloid leukemia (NPM1mut-AML) patients have a high rate of complete remission (CR) to induction chemotherapy. However, the mechanisms responsible for such effects are unknown. Because miR-10 family members are expressed at high levels in NPM1mut-AML, we evaluated whether these microRNAs could predict chemotherapy response in AML. We found that high baseline miR-10 family expression in 54 untreated cytogenetically heterogeneous AML patients was associated with achieving CR. However, when we included NPM1 mutation status in the multivariable model, there was a significant interaction effect between miR-10a-5p expression and NPM1 mutation status. Similar results were observed when using a second cohort of 183 cytogenetically normal older (age ≥ 60 years) AML patients. Loss- and gain-of-function experiments using miR-10a-5p in cell lines and primary blasts did not demonstrate any effect in apoptosis or cell proliferation at baseline or after chemotherapy. These data support a bystander role for the miR-10 family in NPM1mut-AML.
核仁磷酸蛋白突变型急性髓系白血病(NPM1mut-AML)患者对诱导化疗有很高的完全缓解(CR)率。然而,导致这种效果的机制尚不清楚。由于 miR-10 家族成员在 NPM1mut-AML 中高表达,我们评估了这些 microRNAs 是否可以预测 AML 对化疗的反应。我们发现,54 例未经治疗的细胞遗传学异质性 AML 患者的基线 miR-10 家族高表达与获得 CR 相关。然而,当我们将 NPM1 突变状态纳入多变量模型时,miR-10a-5p 表达与 NPM1 突变状态之间存在显著的交互效应。在第二个由 183 例细胞遗传学正常的老年(年龄≥60 岁)AML 患者组成的队列中观察到了类似的结果。使用 miR-10a-5p 在细胞系和原始细胞中的失活和功能获得实验并未显示在基线或化疗后对细胞凋亡或增殖有任何影响。这些数据支持 miR-10 家族在 NPM1mut-AML 中发挥旁观者作用。