ZHOU Chong,ZHOU Ju-ying,WANG Li-li,YU Zhi-ying,XU Xiao-ting,QIN Song-bing,NIE Bin.Study of antisense oligonucleotide miR-21 on radiosensitivity of SHG-44 in vitro[J].Chinese Journal of Radiological Medicine and Protection,2010,30(6):701-704
Study of antisense oligonucleotide miR-21 on radiosensitivity of SHG-44 in vitro
Received:December 18, 2009  
DOI:
KeyWords:Glioma  Radiosensitivity  miR-21  Cell Cycle  Apoptosis
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Author NameAffiliationE-mail
ZHOU Chong Department of Radiation Oncology, First Hospital Affiliated to Soochow University, Suzhou 215006, China  
ZHOU Ju-ying Department of Radiation Oncology, First Hospital Affiliated to Soochow University, Suzhou 215006, China zhjuying@sohu.com 
WANG Li-li Department of Radiation Oncology, First Hospital Affiliated to Soochow University, Suzhou 215006, China  
YU Zhi-ying Department of Radiation Oncology, First Hospital Affiliated to Soochow University, Suzhou 215006, China  
XU Xiao-ting Department of Radiation Oncology, First Hospital Affiliated to Soochow University, Suzhou 215006, China  
QIN Song-bing Department of Radiation Oncology, First Hospital Affiliated to Soochow University, Suzhou 215006, China  
NIE Bin Department of Radiation Oncology, First Hospital Affiliated to Soochow University, Suzhou 215006, China  
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Abstract::
      Objective To investigate the radiosensitizing effect of knock-down the expression of miR-21 on human SHG-44 glioma cells and explore the possible mechanism. Methods Antisense oligonuleotides of miR-21,mediated by LipofectamineTM 2000,were transfected to SHG-44 cells.Three groups were:blank control group(mock group),negative control and antisense transfected group(AS-miR-21 gorup).Cells of each group were irradiated with 6 MeV X-rays at the doses of 0,1,2,4,6 and 8 Gy.Dose-suvivial curve was established by colony-forming assay.The influence of AS-miR-21 on cell cycle and cell apoptosis was analyzed by flow cytometry assay after 6 Gy irradiation.Results The value of D0 and Dq of AS-miR-21 group declined obviously compared with the mock group and negative control group.Flow cytometric analysis showed that cell cycle distribution changed(G0/G1 phase arrest,S phase decreased) after transfected with AS-miR-21(t =8.18,-4.52, P <0.05).The sensitization enhancement ratios of D0 and Dq were 1.32 and 2.10 respectively.Apoptosis assay showed the early apoptosis rate was significantely increased in AS-miR-21、irradition alone and combined group than mock control group(t =20.14,11.11,50.07, P <0.05).Conclusions AS-miR-21 can enhance the radiosensitivity of human glioma cells SHG-44 by promoting cell apoptosis and faciliating cell cycle redistribution.
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