MiR-15b regulates cell differentiation and survival by targeting CCNE1 in APL cell lines

被引:7
作者
Yuan, Zhen [1 ,2 ]
Zhong, Liang [2 ]
Liu, Dongdong [1 ,2 ]
Yao, Juanjuan [1 ]
Liu, Junmei [1 ]
Zhong, Pengqiang [1 ]
Yao, Shifei [1 ]
Zhao, Yi [1 ]
Li, Lianwen [1 ]
Chen, Min [1 ]
Liu, Lu [1 ,2 ]
Liu, Beizhong [1 ,2 ]
机构
[1] Chongqing Med Univ, Yong Chuan Hosp, Cent Lab, Chongqing 402160, Peoples R China
[2] Chongqing Med Univ, Dept Lab Med, Key Lab Lab Med Diagnost, Minist Educ, Chongqing 400016, Peoples R China
基金
中国国家自然科学基金;
关键词
Acute promyelocytic leukemia; miR-15b; All-trans retinoic acid; Differentiation; Proliferation; CCNE1; ACUTE PROMYELOCYTIC LEUKEMIA; RETINOIC ACID; CYCLIN-E; RAR-ALPHA; MICRORNAS; PROLIFERATION; TRANSCRIPTION; TRANSLOCATION; TRANSITION; EXPRESSION;
D O I
10.1016/j.cellsig.2019.04.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
MicroRNAs have been shown to be involved in various cell processes, including proliferation, apoptosis and differentiation. However, little is known about their function in granulopoiesis. In the present study, over expression and knockdown experiments revealed that miR-15b was required to block the proliferation of NB4 and HL60 cells and induce them differentiated to granulocyte lineage. Moreover, we identified CCNE1 as a direct target of miR-15b, and demonstrated that CCNE1 was involved in cell differentiation and proliferation in acute promyelocytic leukemia cells. In addition, we demonstrated a novel pathway in which miR-15b regulated cells arrested in the G0/G1 phase and promoted terminal differentiation of cells by targeting CCNE1, which could modulate the cell cycle effort pRb in APL cells. These events blocked cell proliferation and promoted granulocyte differentiation. In conclusion, our data highlighted, for the first time, the important role of miR-15b in myeloid differentiation and suggested the potential role of miR-15b in cancer therapy.
引用
收藏
页码:57 / 64
页数:8
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