Zhang Chaoxiong,Zhang Mingjian,Gao Fu,Zhou Chuanfeng,Zhang Pei,Cai Jianming,Liu Cong.Down regulation of miR-203 in radiation- induced thymic lymphoma promoted cells proliferation and inhibited apoptosis[J].Chinese Journal of Radiological Medicine and Protection,2015,35(1):28-34
Down regulation of miR-203 in radiation- induced thymic lymphoma promoted cells proliferation and inhibited apoptosis
Received:September 01, 2014  
DOI:10.3760/cma.j.issn.0254-5098.2015.01.005
KeyWords:MiR-203  Radiation-induced thymic lymphoma (RITL)  TANK-binding kinase 1 (TBK1)  SLUG (SNAI2)  Cyclin D1 (CCND1)
FundProject:This work was supported by grant from National Natural Science Foundation of China (81402630).
Author NameAffiliationE-mail
Zhang Chaoxiong Department of Radiation Medicine, Faculty of Naval Medicine, Second Military Medical University, Shanghai 200433  
Zhang Mingjian Xingcheng Sanatorium of Shenyang Military Region  
Gao Fu Department of Radiation Medicine, Faculty of Naval Medicine, Second Military Medical University, Shanghai 200433  
Zhou Chuanfeng Department of Radiation Medicine, Faculty of Naval Medicine, Second Military Medical University, Shanghai 200433  
Zhang Pei Department of Radiation Medicine, Faculty of Naval Medicine, Second Military Medical University, Shanghai 200433  
Cai Jianming Department of Radiation Medicine, Faculty of Naval Medicine, Second Military Medical University, Shanghai 200433  
Liu Cong Department of Radiation Medicine, Faculty of Naval Medicine, Second Military Medical University, Shanghai 200433 victorliu20102020@163.com 
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Abstract::
      Objective To investigate the role of miR-203 in radiation-induced thymic lymphoma (RITL).Methods A 60Co irradiator was used for total-body irradiation. MicroRNAs(miRNAs) level was assayed by qRT-PCR. Cell proliferation was assayed by MTT assay. Cell apoptosis was examined by fluorescence activated cell sorter(FACS). Dual luciferase reporter assay system was used to detect the 3'UTR reporter. Results MiR-203 was down-regulated in RITL tissues. Overexpression of miR-203 strongly inhibited the proliferation of both NIH3T3 cells and EL4 cells and vice versa. MiR-203 inhibited cells proliferation and induced apoptosis via TANK-binding kinase (TBK1), SLUG(SNAI2) and Cyclin D1(CCND1). Conclusions Radiation down-regulated the level of miR-203 in thymic, which promoted radiation-induced thymic lymphoma by targeting TBK1, SNAI2 and CCND1.
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