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肿瘤细胞对DNA拓扑异构酶Ⅰ抑制剂的耐药研究进展 被引量:1

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摘要 DNA拓扑异构酶(Topo)抑制剂作为一种新的抗癌靶点,在恶性肿瘤的治疗中有广阔的应用前景,然而耐药性的出现极大限制了其临床应用。Topo分Ⅰ,Ⅱ两型,就Topo Ⅰ抑制剂的耐药机理及可能的逆转途径进行综述。
作者 贾平 马丁
出处 《国外医学(妇产科学分册)》 CAS 2004年第1期32-35,共4页 Foreign Medical Sciences(Obstet Gynecol Fascicle)
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参考文献21

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同被引文献5

  • 1Chang JY, Liu JF, Juang SH, et al. Novel mutation of topoi-somerase I in rendering cells resistant to camptothecin[ J]. Cancer Res, 2002,62:3716-3721.
  • 2Urasaki Y, Iaco GS, Pourquier P, et al. Characterization of a novel topoisomerase I mutation from a camptothecin-resistant human prostate cancer ceil line[ J]. Cancer Res, 2001,61:1964-1969.
  • 3LaUoo AK, Luo FR, Guo A, et al. Membrane transport of camptothecin: facilitation by human P-glycoprotein( ABCB1 ) and multidrug resistance protein 2 (ABCC2) [ J ]. BMC Med, 2004,2 : 16.
  • 4樊代明,刘宪玲.胃癌多药耐药研究新进展[J].中华消化杂志,2000,20(2):77-78. 被引量:5
  • 5涂水平,江石湖,谭继宏,钟捷,乔敏敏,蒋晓华,章永平,袁耀宗,吴云林,吴裕炘.羟基喜树碱诱导胃癌细胞凋亡的作用机制初步研究[J].中华消化杂志,2001,21(5):274-277. 被引量:25

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