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拓扑异构酶Ⅱ与头颈肿瘤化疗的研究进展 被引量:1

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摘要 头颈肿瘤化疗失败的主要原因是多药耐药(MDR),拓扑异构酶Ⅱ(ToPoⅡ)表达异常是引起多药耐药的主要机制之一,称为不典型耐药(at-MDR)。本文就ToPoⅡ的生物学特性、介导at-MDR的机制及以ToPoⅡ为作用靶点的抗肿瘤药物等方面进行综述。
出处 《内蒙古医学院学报》 2005年第6期33-35,共3页 Acta Academiae Medicinae Neimongol
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同被引文献6

  • 1邓刚,杨成章,陈望燕.Ki-67和拓扑异构酶Ⅱα在喉鳞状细胞癌中的表达及意义[J].临床耳鼻咽喉科杂志,2005,19(9):396-398. 被引量:2
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  • 3Horibe Y,Murakami M,Komori K. Expression of topoisomerase Ⅱ alpha,Ki-67 and p53 in early stage laryngeal carcinomas not featuring vocal cord fixation[J].Acta Pathologica,Microbiologica Et Immunologica Scandinavica,2000,(10):689-696.
  • 4Shvero J,Koren R,Shvili Ⅰ. Expression of human DNA Topoisomerase Ⅱ-alpha in squamous cell carcinoma of the larynx and its correlation with clinicopathologic variables[J].American Journal of Clinical Pathology,2008,(06):934-939.doi:10.1309/AJCPROG61USKCBEI.
  • 5郭亚青.Mdm2 PARP ToPoⅡ在喉癌中的表达及临床意义[DB]中国优秀硕士学位论文全文数据库,20061-14.
  • 6唐平章,王晓雷.中国头颈肿瘤治疗60年巡礼[J].中华耳鼻咽喉头颈外科杂志,2009,44(10):805-807. 被引量:3

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