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收稿:2018-01-25,
纸质出版:2018-08-30
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邹德伟, 王俊伟, 汪攀, 等. 阿司匹林对小鼠胶质瘤干细胞增殖及凋亡的体外研究[J]. 第三军医大学学报, 2018,40(16):1456-1460.
Dewei ZOU, Junwei WANG, Pan WANG, et al. Effects of aspirin on proliferation and apoptosis of mouse glioma stem cells
邹德伟, 王俊伟, 汪攀, 等. 阿司匹林对小鼠胶质瘤干细胞增殖及凋亡的体外研究[J]. 第三军医大学学报, 2018,40(16):1456-1460. DOI: 10.16016/j.1000-5404.201801221.
Dewei ZOU, Junwei WANG, Pan WANG, et al. Effects of aspirin on proliferation and apoptosis of mouse glioma stem cells
Objective
2
To study the effects of aspirin on proliferation and apoptosis of mouse glioma stem cells (GSCs).
Methods
2
In vitro
cultured GSCs isolated from mouse glioma cell line GL261 were treated with 2.5
5.0 and 10 mmol/L aspirin
with normal saline as the control.The pro
liferation of GSCs was assayed using CCK-8 kit
and the changes in cell cycle distribution and cell apoptosis were detected with flow cytometry and TUNEL assay
respectively; LDH kit was used to assess the cell damage after aspirin treatment.
Results
2
Compared with the control cells
the GSCs treated with different concentrations of aspirin showed dose- and time-dependent inhibition of cell proliferation (
P
<
0.05) and obviously reduced number and size of the tumor spheres (
P
<
0.05).Aspirin caused obvious cell cycle changes in GSCs
shown by a significantly decreased percentage of S phase cells and an increased percentage of G
0
/G
1
phase cells (
P
<
0.05).Aspirin also induced obvious apoptosis of GSCs and significantly increased the release of cytosolic LDH (
P
<
0.05).
Conclusion
2
Aspirin inhibits the proliferation and promotes apoptosis of mouse GSCs
in vitro
.
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WANG Y HUANG N X LI H L Promoting oligodendroglial-oriented differentiation of glioma stem cell: a repurposing of quetiapine for the treatment of malignant glioma Oncotarget 2017 8 23 37511 3752 10.18632/oncotarget.16400 WANG Y, HUANG N X, LI H L, et al . Promoting oligodendroglial-oriented differentiation of glioma stem cell: a repurposing of quetiapine for the treatment of malignant glioma[J ] . Oncotarget, 2017, 8(23): 37511-3752. DOI: 10.18632/oncotarget.16400.
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