Fan Sheng-Jin, Li Hui-Bo, Cui Gang, Kong Xiao-Lin, Sun Li-Li, Zhao Yan-Qiu, Li Ying-Hua, Zhou Jin
Department of Hematology, The First Clinical Hospital Affiliated to Harbin Medical University, Harbin 150001, Heilongjiang, PR China.
Department of Hematology, The First Clinical Hospital Affiliated to Harbin Medical University, Harbin 150001, Heilongjiang, PR China.
Leuk Res. 2016 Feb;41:62-70. doi: 10.1016/j.leukres.2015.11.016. Epub 2015 Dec 1.
MicroRNA-149* (miRNA-149*) functions as an oncogenic regulator in human melanoma. However, the effect of miRNA-149* on T-cell acute lymphoblastic leukemia (T-ALL) is unclear. Here we aimed to analyze the effects of miRNA-149* on in vitro T-ALL cells and to uncover the target for miRNA-149* in these cells. The miRNA-149* level was determined in multiple cell lines and bone marrow cells derived from patients with T-ALL, B acute lymphoblastic leukemia (B-ALL), acute myelocytic leukemia (AML), and healthy donors. We found that miRNA-149* was highly expressed in T-ALL cell lines and T-ALL patients' bone marrow samples. JunB was identified as a direct target of miR-149*. miRNA-149* mimics downregulated JunB levels in Molt-4 and Jurkat cells, while miRNA-149* inhibitors dramatically upregulated JunB expression in these cells. miRNA-149* mimics promoted proliferation, decreased the proportion of cells in G1 phase, and reduced cell apoptosis in T-ALL cells, while miRNA-149* inhibitors prevented these effects. miRNA-149* mimics downregulated p21 and upregulated cyclinD1, 4EBP1, and p70s6k in Molt-4 and Jurkat cells. Again, inhibitors prevented these effects. Our findings demonstrate that miRNA-149* may serve as an oncogenic regulator in T-ALL by negatively regulating JunB.
微小RNA-149*(miRNA-149*)在人类黑色素瘤中作为一种致癌调节因子发挥作用。然而,miRNA-149对T细胞急性淋巴细胞白血病(T-ALL)的影响尚不清楚。在此,我们旨在分析miRNA-149对体外T-ALL细胞的影响,并揭示miRNA-149在这些细胞中的靶标。在源自T-ALL、B急性淋巴细胞白血病(B-ALL)、急性髓细胞白血病(AML)患者以及健康供体的多种细胞系和骨髓细胞中测定了miRNA-149水平。我们发现miRNA-149在T-ALL细胞系和T-ALL患者的骨髓样本中高表达。JunB被鉴定为miR-149的直接靶标。miRNA-149模拟物下调了Molt-4和Jurkat细胞中的JunB水平,而miRNA-149抑制剂则显著上调了这些细胞中JunB的表达。miRNA-149模拟物促进了T-ALL细胞的增殖,降低了G1期细胞的比例,并减少了细胞凋亡,而miRNA-149抑制剂则阻止了这些作用。miRNA-149模拟物下调了Molt-4和Jurkat细胞中的p21并上调了细胞周期蛋白D1、4EBP1和p70s6k。同样,抑制剂阻止了这些作用。我们的研究结果表明,miRNA-149可能通过负向调节JunB在T-ALL中作为致癌调节因子发挥作用。