Jiang Xueke, Jing Yipei, Lei Li, Peng Meixi, Xiao Qiaoling, Ren Jun, Tao Yonghong, Huang Junpeng, Zhang Ling
Key Laboratory of Clinical Laboratory Diagnostics Designated by the Ministry of Education, School of Laboratory Medicine, Chongqing Medical University, Chongqing 400016, China.
Key Laboratory of Clinical Laboratory Diagnostics Designated by the Ministry of Education, School of Laboratory Medicine, Chongqing Medical University, Chongqing 400016, China. *Corresponding author, E-mail:
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2021 Oct;37(10):881-890.
Objective To investigate the effect of miR-148b-3p on the proliferation and autophagy of acute myeloid leukemia (AML) cells and its molecular mechanism. Methods Based on GEO and TCGA databases, the expression of miR-148b-3p in AML cells and its association with clinical prognosis of patients were analyzed with the bioinformatics software. The expression of miR-148b-3p in AML cells was detected by real-time quantitative PCR. The miR-148b-3p mimic and the miR-148b-3p inhibitor were transiently transfected into AML cell lines THP-1 and NB4 by liposome-mediated transfection, respectively. The proliferation of leukemia cells was evaluated by CCK-8 assay and 5-ethynyl-2'-deoxyuridine (EdU) labeling, and the protein levels of Bcl2, Bcl2-associated X protein (BAX), autophagy marker LC3, P62, and autophagy-related gene 14 (ATG14) were detected by Western blotting. The targeted binding of miR-148b-3p to ATG14 was measured by dual-luciferase reporter gene assay, and the effect of miR-148b-3p/ATG14 axis on the phenotype of AML cells was observed in the rescue experiments. Results A decreased expression of miR-148b-3p was found in leukemia blasts of AML patients, and the overall survival rate of AML patients with low expression of miR-148b-3p was significantly lower than that of the control group. Overexpression of miR-148b-3p inhibited THP-1 cells proliferation, promoted their apoptosis, downregulated the LC3II and ATG14 protein levels, and upregulated the P62 protein levels, while inhibiting the expression of miR-148b-3p in NB4 cells had the opposite effect. miR-148b-3p significantly reduced the luciferase activity of the wild-type ATG14 expression vector. The results of rescue experiments showed that overexpression of ATG14 reversed the inhibitory effect of miR-148b-3p upregulation on cell proliferation and autophagy, while inhibition of ATG14 expression weakened the promotive effect of miR-148b-3p downregulation on cell phenotype. Conclusion The miR-148b-3p inhibits the in vitro proliferation and autophagy of AML cells by targeting ATG14.
目的 探讨miR-148b-3p对急性髓系白血病(AML)细胞增殖和自噬的影响及其分子机制。方法 基于GEO和TCGA数据库,使用生物信息学软件分析miR-148b-3p在AML细胞中的表达及其与患者临床预后的关系。通过实时定量PCR检测AML细胞中miR-148b-3p的表达。分别采用脂质体介导的转染方法将miR-148b-3p模拟物和miR-148b-3p抑制剂瞬时转染至AML细胞系THP-1和NB4中。通过CCK-8法和5-乙炔基-2'-脱氧尿苷(EdU)标记评估白血病细胞的增殖情况,采用蛋白质印迹法检测Bcl2、Bcl2相关X蛋白(BAX)、自噬标志物LC3、P62和自噬相关基因14(ATG14)的蛋白水平。通过双荧光素酶报告基因检测法检测miR-148b-3p与ATG14的靶向结合情况,并在拯救实验中观察miR-148b-3p/ATG14轴对AML细胞表型的影响。结果 发现AML患者白血病原始细胞中miR-148b-3p表达降低,miR-148b-3p低表达的AML患者总生存率显著低于对照组。miR-148b-3p过表达抑制THP-1细胞增殖,促进其凋亡,下调LC3II和ATG14蛋白水平,上调P62蛋白水平,而抑制NB4细胞中miR-148b-3p的表达则产生相反的效果。miR-148b-3p显著降低野生型ATG14表达载体的荧光素酶活性。拯救实验结果显示,ATG14过表达逆转了miR-148b-3p上调对细胞增殖和自噬的抑制作用,而抑制ATG14表达则削弱了miR-148b-3p下调对细胞表型的促进作用。结论 miR-148b-3p通过靶向ATG14抑制AML细胞的体外增殖和自噬。