TANG Gu-Sheng,CAI Jian-Ming,NI Jin.Study on radiosensitivity of B16 cells transfected by STAT3 antisense oligodeoxynucleotides[J].Chinese Journal of Radiological Medicine and Protection,2006,26(4):324-327
Study on radiosensitivity of B16 cells transfected by STAT3 antisense oligodeoxynucleotides
Received:January 08, 2006  
DOI:
KeyWords:ASO-STAT3  B16  Radiosensitivity  Apoptosis  Tumor therapy
FundProject:国家自然科学基金资助项目(30470415)
Author NameAffiliationE-mail
TANG Gu-Sheng Department of Radiation and Nuclear Medicine, The Second Military Medical University, Shanghai 200433, China cjm882003@yahoo.com.cn 
CAI Jian-Ming Department of Radiation and Nuclear Medicine, The Second Military Medical University, Shanghai 200433, China  
NI Jin Department of Radiation and Nuclear Medicine, The Second Military Medical University, Shanghai 200433, China  
吴君 第二医科大学附属仁济医院急诊科  
项莺松 Department of Radiation and Nuclear Medicine, The Second Military Medical University, Shanghai 200433, China  
崔建国 Department of Radiation and Nuclear Medicine, The Second Military Medical University, Shanghai 200433, China  
单鹄声 Department of Radiation and Nuclear Medicine, The Second Military Medical University, Shanghai 200433, China  
赵芳 Department of Radiation and Nuclear Medicine, The Second Military Medical University, Shanghai 200433, China  
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Abstract::
      Objective To investigate the influence of STAT3 antisense oligodeoxynucleotides (ASO-STAT3) on radiosensitivity of B16 cells. Methods Oligodeoxynucleotides were tansfected into B16 cells with oligofectamine reagent. Cell survival was measured using CCK-8 assay. Apoptotic assays were performed using Hoechst33258 staining and Annexin V/PI with FACS analysis. Results Cell survival decreased significantly in those groups tansfected with ASO-STAT3 and irradiated with different dose of γ-rays. Compared with those cells treated with irradiation alone or AO-STAT3 transfection with subsequent exposure to radiation, fraction of early apoptosis increased in those cells treated with ASO-STAT3 transfection combined with irradiation. Conclusion These results showed that targeting ASO-STAT3 can enhance the therapeutic effect of γ-ray irradiation on B16 cells, which implied that STAT3 can act as a potential molecular target for tumor therapies, and also a potential molecular target for enhancement of radiosensitivity of radioresistant tumors.
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