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胶质瘤的靶向性基因治疗进展

The development of targeted gene therapy in gliomas
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摘要 在胶质瘤的基因治疗中,利用脑胶质瘤组织中相对特异性的标志物如表皮生长因子受体、端粒及端粒酶等实现目的基因在肿瘤组织的靶向性表达;同时对病毒载体进行重组,对肿瘤血管生成的抑制等实现选择性地、高效地对肿瘤组织的转染。 In gene therapy, gene transfer is targeted into specific tumor tissue by using relatively specific markers in brain gliomas such as EGFR, telomere and telomerase. At the same time, viral vectors are recombined and antiangiogenesis is adopted, which makes transfection into gliomas more efficient and selective.
作者 买正军 孙涛
出处 《中华神经医学杂志》 CAS CSCD 2003年第5期390-391,395,共3页 Chinese Journal of Neuromedicine
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  • 1符伟军,洪宝发,黄君健,徐兵,高江平,王晓雄.端粒酶反义RNA基因转染抑制裸鼠人膀胱癌移植瘤生长的研究[J].中华实验外科杂志,2003,20(11):1021-1022. 被引量:3
  • 2Carol A. Kruse,Dawn H. Mitchell,Bette K. Kleinschmidt-DeMasters,Wilbur A. Franklin,Helvise G. Morse,Elaine B. Spector,Kevin O. Lillehei. Characterization of a continuous human glioma cell line DBTRG-05MG: growth kinetics, karyotype, receptor expression, and tumor suppressor gene analyses[J] 1992,In Vitro Cellular & Developmental Biology - Animal(9-10):609~614

二级参考文献2

  • 1Elenitoba-Johnson KS. Complex regulation of telomerase activity: implications for cancer therapy. Am J Pathol, 2001, 159:405-410.
  • 2Koga S, Kondo Y, Komata T, et al.Treatment of bladder cancer cells in vitro and in vivo with 2-5A antisense telomerase RNA. Gene Ther,2001,8:654-658.

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