LI Feng-sheng,GAO Ling,SONG Xiu-jun,LI Xiao,JIANG Qi-sheng,CHEN Xiao-hua.Effect of ionizing radiation on the expressions of STAT3 target genes in A549 cells[J].Chinese Journal of Radiological Medicine and Protection,2013,33(5):472-475
Effect of ionizing radiation on the expressions of STAT3 target genes in A549 cells
Received:May 16, 2013  
DOI:10.3760/cma.j.issn.0254-5098.2013.05.004
KeyWords:Ionizing radiation  STAT3  VEGF  Survivin
FundProject:国家自然科学基金(8120215,81172130,81001216)
Author NameAffiliationE-mail
LI Feng-sheng The PLA Research Center for Medical Monitoring and Prevention of Nuclear Radiation Damage, The Second Artillery General Hospital, Beijing 100088, China  
GAO Ling 中国疾病预防控制中心辐射防护与核医学安全所 辐射防护与核应急中国疾病预防控制中心重点实验室  
SONG Xiu-jun The PLA Research Center for Medical Monitoring and Prevention of Nuclear Radiation Damage, The Second Artillery General Hospital, Beijing 100088, China  
LI Xiao The PLA Research Center for Medical Monitoring and Prevention of Nuclear Radiation Damage, The Second Artillery General Hospital, Beijing 100088, China  
JIANG Qi-sheng The PLA Research Center for Medical Monitoring and Prevention of Nuclear Radiation Damage, The Second Artillery General Hospital, Beijing 100088, China  
CHEN Xiao-hua 军事医学科学院放射与辐射医学研究所 Chenxh0676@sina.com 
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Abstract::
      Objective To investigate the effect of ionizing radiation on the expression of transcription factor STAT3 target genes in the pulmonary adenocarcinoma cell line A549. Methods The expressions of VEGF, Bcl-2 and Survivin in A549 cells with or without STAT3 inhibition were detected by RT-PCR and/or Western blot 24 h after 2 or 4 Gy of γ-ray irradiation. Results After γ-ray irradiation with 2 or 4 Gy, the expression of VEGF and Survivin increased significantly. However, the expression of Bcl-2 was not affected by γ-ray irradiation. Furthermore, the increased expression of VEGF and Survivin induced by radiation was found to be inhibited after radiation-induced activation of STAT3 was blocked by AG490 inhibiter. Conclusions γ-ray irradiation could up-regulate the expression of Survivin and VEGF via activating STAT3. The increase of Survivin might partly inhibit the radiation-induced apoptosis of A549 cells, and the up-regulation of VEGF might contribute to the tumor angiogenesis.
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