期刊文献+

pEgr-angiostatin基因辐射诱导表达特性及其抗肿瘤作用 被引量:6

Expression Property and Antitumor Effect of pEgr-angiostatin Induced by Ionizing Radiation
在线阅读 下载PDF
导出
摘要 目的 :检测 p Egr- angiostatin重组质粒在 B1 6细胞中的辐射诱导表达和观察 p Egr-angiostatin基因 -放射治疗的抗肿瘤作用。方法 :用 RT- PCR方法从小鼠肝脏中扩增出 angiostatinc DNA,经测序证实后 ,构建 p Egr- angiostatin重组质粒 ,脂质体介导的转染法转染小鼠 B1 6细胞 ,检测 B1 6细胞内 angiostatin m RNA的辐射诱导表达 ,体内观察 p Egr- angiostatin基因 -放射治疗的抑瘤作用。结果 :测序表明扩增的 angiostatin c DNA序列与报道基本一致 ,Egr- 1启动子和 angiostatinc DNA正确插入表达载体 pc DNA3.1 ,转染 B1 6细胞内 angiostatin m RNA的表达具有辐射诱导特性 ,p Egr- angiostatin基因 -放射治疗荷瘤小鼠具有明显的抑瘤作用。结论 :成功地克隆小鼠angiostatin基因 ,并证实 p Egr- angiostatin的辐射诱导表达规律及其基因 Objective:To study on the expression and antitumor effect of pEgr angiostatin induced with ionizing radiation. Methods:Mouse angiostatin cDNA was amplified with RT PCR. The pEgr angiostatin recombinant plasmid was constructed and was then transfected into B16 cells with liposome. The cells were irradiated and the expression of angiostatin mRNA in B16 cells was detected. Finally, the antitumor effect of pEgr angiostatin was studied. Results:The sequence of mouse angiostatin cDNA was identical to reported. Egr 1 promoter and angiostatin cDNA was inserted correctly into expression vector. The expression property of pEgr angiostatin was examined by ionizing radiation. The gene therapy with pEgr angiostatin showed remarkably antitumor effect.Conclusion:Mouse angiostatin cDNA had been cloned successfully in the study.The expression property and the antitumor effect of pEgr angiostatin are induced by ionizing radiation. This result provides the basis for multi gene radiotherapy of tumor. [
出处 《吉林大学学报(医学版)》 CAS CSCD 北大核心 2003年第5期543-546,共4页 Journal of Jilin University:Medicine Edition
基金 国家自然科学基金资助课题 (30 170 2 90 )
关键词 小鼠 血管抑素 EGR-1启动子 pEgr-angiostatin重组质粒 基因-放射治疗 Mouse angiostatin Egr 1 promoter pEgr angiostatin Gene radiotherapy
  • 相关文献

参考文献4

二级参考文献26

  • 1李修义,傅海青,刘树铮.低剂量全身照射增强荷瘤小鼠局部大剂量照射的抑瘤作用[J].白求恩医科大学学报,1995,21(6):559-562. 被引量:21
  • 2[1]O′Reilly MS,Boehm T,Shing Y,et al.Endostatin: an endogenous inhibitor of angiogenesis and tumor growth[J].Cell,1997,88(2):277-285.
  • 3[2]O′Reilly MS,Holmgren L,Shing Y,et al.Angiostatin: a novel angiogenesis inhibitor that mediates the suppression of metastases by a Lewis lung carcinoma[J].Cell,1994,79(2):315-328.
  • 4[3]Chen QR,Kumar D,Stass SA,et al.Liposomes complexed to plasmids encoding angiostatin and endostatin inhibit breast cancer in nude mice[J].Cancer Res,1999,59(14):3308-3319.
  • 5[4]Sauter BV,Martinet O,Zhang WJ,et al.Adenovirus-mediated gene transfer of endostatin in vivo results in high level of transgene expression and inhibition of tumor growth and metastases[J].Proc Natl Acad Sci ,2000,97(9):4902-4807.
  • 6[5]Bergers G,Javaherian K,Lo KM,et al.Effects of angiogenesis inhibitors on multistage carcinogenesis in mice[J].Science,2000,284(5415):808-811.
  • 7[6]Weichselbaum RR,Hallahan DE.Gene therapy targeted by radiation preferentially radiosensitizes tumor cells[J].Cancer Res,1994,54:4266-4269.
  • 8[7]Takahashi T,Namiki Y,Ohno T.Induction of the suicide HSV-TK gene by activation of the Egr-1 promoter with radioisotopes[J].Hum Gene Ther,1997,8:827-831.
  • 9[8]Chen QR,Kumar D,Stass SA,et al.Liposomea complexed to plamids encoding angiostatin and endostatin inhibit breast cancer in nude mice[J].Cancer Res,1999,59:3308-3312.
  • 10[9]Kerbel RS.A cancer therapy resistant to resistance[J].Nature,1997,390(6658):335-338.

共引文献8

同被引文献34

  • 1朴春姬,田梅,刘林林,杨巍,李修义1.辐射诱导表达载体pEgr-hTRAIL的构建及其对肿瘤细胞的体外诱导凋亡作用[J].吉林大学学报(医学版),2005,31(2):169-172. 被引量:7
  • 2王贵全,许传杰,杨文,朴春姬,董震.pEgr-sHemopexin重组质粒的构建及体外辐射诱导表达[J].吉林大学学报(医学版),2005,31(2):236-238. 被引量:1
  • 3董丽华,付士波,杨英,刘扬,龚守良.pcEgr-hp53辐射诱导表达载体的构建及其体外抗肿瘤的作用[J].中国实验诊断学,2006,10(2):111-114. 被引量:1
  • 4田梅,朴春姬,刘林林,杨巍,李修义.pEgr-hPTEN稳定转染联合辐射诱导人胶质瘤SHG-44细胞凋亡及Bcl-2表达下调[J].中华放射医学与防护杂志,2006,26(2):106-109. 被引量:4
  • 5Weichselbaum RR, Fuks Z, Hallagan DE,et al. Racliation-induced cytokincs and growth factors:Cellular and molecular basis of the modification of radiation damage [A]. In: Yamold J, Steatton J, McMillan T. Molecular Biology for Oncologists[ C]. Amsterdam: Elsevier Science Pub B V, 1993:213 - 221.
  • 6Scott SD, Marples B, Hendry JH, et al.A radiation controlled molecular switch for use in gene therapy of cancer[J]. Gene Ther,2000,7:1121.
  • 7Husain A, Rosales N, Schwartz GK, et al. Lisofylline sensitizes p53 mutant human ovarian carcinoma cells to the cytotoxic effects of cis-diamminedichloroplatinum (II), 1998,70( 1 ) : 17.
  • 8Takahashi T, Namiki Y, Ohno T. Induction of the suicide HSV- TK gene by activation of the Egr-1 promoter with radioisotopes. Hum Gene Ther, 1997, 8 (7) :827-833.
  • 9Brooks PC, Silletti S, yon Schalscha TL, et al. Disruption of angiogenesis by PEX, a noncatalytic metalloproteinase fragment with integrin binding activity. Cell, 1998,92(3) :391-400.
  • 10Boehm T, Folkman J, Browder T, et al. Antiangiogenic therapy of experimental cancer does not induce acquired drug resistance. Nature, 1997,390(6658) :404-407.

引证文献6

二级引证文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部