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miR-34a通过Notch1信号通路对肺癌干细胞的抑制
引用本文:韩纪昌,张祎捷,李红兵,杨存葆,马超楠,戚冠斌. miR-34a通过Notch1信号通路对肺癌干细胞的抑制[J]. 中国组织工程研究, 2016, 20(23): 3349-3356. DOI: 10.3969/j.issn.2095-4344.2016.23.001
作者姓名:韩纪昌  张祎捷  李红兵  杨存葆  马超楠  戚冠斌
作者单位:河南大学淮河医院呼吸内科,河南省开封市 475000
基金项目:河南省卫生厅中青年科技创新人才工程(4189号)
摘    要:


关 键 词:干细胞  肿瘤干细胞  肺癌干细胞  miRNA  miR-34a  Notch1信号通路  Notch1  肺腺癌A549细胞  CD133+肺癌干细胞  增殖  凋亡  
收稿时间:2016-04-19

Inhibitory effect of miR-34a on lung cancer stem cells via Notch1 signaling pathway
Han Ji-chang,Zhang Yi-jie,Li Hong-bing,Yang Cun-bao,Ma Chao-nan,Qi Guan-bin. Inhibitory effect of miR-34a on lung cancer stem cells via Notch1 signaling pathway[J]. Chinese Journal of Tissue Engineering Research, 2016, 20(23): 3349-3356. DOI: 10.3969/j.issn.2095-4344.2016.23.001
Authors:Han Ji-chang  Zhang Yi-jie  Li Hong-bing  Yang Cun-bao  Ma Chao-nan  Qi Guan-bin
Affiliation:Department of Respiratory Medicine, Huaihe Hospital of Henan University, Kaifeng 475000, Henan Province, China
Abstract:
BACKGROUND:It has been proved that miR-34a plays an inhibitory role in the growth of lung cancer stem cells, but the underlying mechanism remains unclear.OBJECTIVE:To explore the inhibitory effect of miR-34a on lung cancer stem cells and the underlying mechanism. METHODS:The CD133+ lung cancer stem cells were separated from lung cancer A549 cell lines using magnetic activated cell sorting method. And miR-34a-overexpressing CD133+ lung cancer stem cells were established by liposome transfection technology. Besides, the targeted relationship between miR-34a and Notch1 was analyzed by the dual-luciferase reporter. Afterwards, Notch1 silencing was performed by gene knockout, and its effect on lung cancer stem cells was determined.RESULTS AND CONCLUSION:After sorted and detected by immunomagetic selection and flow cytometry assay respectively, a high rate of CD133+ lung cancer stem cell was obtained. And qRT-PCR detected that the expression level of miR-34a in CD133+ lung cancer stem cells was significantly lower than that in CD133- lung cancer stem cells. Moreover, miR-34a-overexpressing CD133+ lung cancer stem cells were successfully constructed and miR-34a significantly inhibited proliferation and induced apoptosis of lung cancer stem cells. Dual-luciferase reporter assay indicated that Notch1 mRNA was a target of miR-34a. In addition, Notch1 silencing obviously inhibited proliferation and induced apoptosis of lung cancer stem cells. These findings suggest that miR-34a can inhibite lung cancer stem cells via the Notch1 signaling pathway.
Keywords:Lung Neoplasms   Neoplastic Stem Cells  MicroRNAs   Receptors   Notch1   Tissue Engineering  
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