miRNA-149 promotes cell proliferation and suppresses apoptosis by mediating JunB in T-cell acute lymphoblastic leukemia

被引:57
作者
Fan, Sheng-jin [1 ]
Li, Hui-bo [1 ]
Cui, Gang [1 ]
Kong, Xiao-lin [1 ]
Sun, Li-li [1 ]
Zhao, Yan-qiu [1 ]
Li, Ying-hua [1 ]
Zhou, Jin [1 ]
机构
[1] Harbin Med Univ, Dept Hematol, Clin Hosp Affiliated 1, 13th Floor,1st Bldg,23 Youzheng St, Harbin 150001, Heilongjiang, Peoples R China
关键词
miRNA-149; JunB; T-ALL; Proliferation; Apoptosis; MICRORNAS; EXPRESSION; LYMPHOMA; DISEASE; AKT1;
D O I
10.1016/j.leukres.2015.11.016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 down regulated 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 cyclinDl, 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. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:62 / 70
页数:9
相关论文
共 29 条
[1]   Constitutive control of AKT1 gene expression by JUNB/CJUN in ALK plus anaplastic large-cell lymphoma: a novel crosstalk mechanism [J].
Atsaves, V. ;
Zhang, R. ;
Ruder, D. ;
Pan, Y. ;
Leventaki, V. ;
Rassidakis, G. Z. ;
Claret, F. X. .
LEUKEMIA, 2015, 29 (11) :2162-2172
[2]   The oncogenic JUNB/CD30 axis contributes to cell cycle deregulation in ALK plus anaplastic large cell lymphoma [J].
Atsaves, Vassilis ;
Lekakis, Lazaros ;
Drakos, Elias ;
Leventaki, Vasiliki ;
Ghaderi, Mehran ;
Baltatzis, George E. ;
Chioureas, Dimitris ;
Jones, Dan ;
Feretzaki, Marianna ;
Liakou, Chryssoula ;
Panayiotidis, Panayiotis ;
Gorgoulis, Vassilis ;
Patsouris, Efstratios ;
Medeiros, L. Jeffrey ;
Claret, Francois X. ;
Rassidakis, George Z. .
BRITISH JOURNAL OF HAEMATOLOGY, 2014, 167 (04) :514-523
[3]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[4]   Role for a bidentate ribonuclease in the initiation step of RNA interference [J].
Bernstein, E ;
Caudy, AA ;
Hammond, SM ;
Hannon, GJ .
NATURE, 2001, 409 (6818) :363-366
[5]   Loss of stromal JUNB does not affect tumor growth and angiogenesis [J].
Braun, Jennifer ;
Strittmatter, Karin ;
Nuebel, Tobias ;
Komljenovic, Dorde ;
Sator-Schmitt, Melanie ;
Baeuerle, Tobias ;
Angel, Peter ;
Schorpp-Kistner, Marina .
INTERNATIONAL JOURNAL OF CANCER, 2014, 134 (06) :1511-1516
[6]   MicroRNA signatures in human cancers [J].
Calin, George A. ;
Croce, Carlo M. .
NATURE REVIEWS CANCER, 2006, 6 (11) :857-866
[7]  
Cao R., 2010, J NEUROSCI, V30, P6302
[8]   MicroRNAs act complementarily to regulate disease-related mRNA modules in human diseases [J].
Chavali, Sreenivas ;
Bruhn, Soren ;
Tiemann, Katrin ;
Saetrom, Pal ;
Barrenas, Fredrik ;
Saito, Takaya ;
Kanduri, Kartiek ;
Wang, Hui ;
Benson, Mikael .
RNA, 2013, 19 (11) :1552-1562
[9]   A 3-microRNA scoring system for prognostication in de novo acute myeloid leukemia patients [J].
Chuang, M-K ;
Chiu, Y-C ;
Chou, W-C ;
Hou, H-A ;
Chuang, E. Y. ;
Tien, H-F .
LEUKEMIA, 2015, 29 (05) :1051-1059
[10]   JunB protects β-cells from lipotoxicity via the XBP1-AKT pathway [J].
Cunha, D. A. ;
Gurzov, E. N. ;
Naamane, N. ;
Ortis, F. ;
Cardozo, A. K. ;
Bugliani, M. ;
Marchetti, P. ;
Eizirik, D. L. ;
Cnop, M. .
CELL DEATH AND DIFFERENTIATION, 2014, 21 (08) :1313-1324