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靶向MDR1基因的小分子干扰RNA对卵巢上皮性癌裸鼠移植瘤多药耐药的抑制作用 被引量:1

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摘要 化疗是治疗晚期卵巢上皮性癌(卵巢癌)的重要手段,但多药耐药的产生常使化疗不能达到理想的效果,而多药耐药基因——MDR1基因编码的P糖蛋白(P—gp)的过度表达是导致肿瘤细胞耐药的最直接原因。已有研究表明,小分子干扰RNA(siRNA)可诱导序列特异性基因沉默。在以往的研究中,本研究组利用脂质体介导的siRNA在体外成功地转染卵巢癌耐药细胞株,并证实了其具有诱导MDR1基因沉默、逆转卵巢癌细胞耐药的作用。本研究建立了耐药卵巢癌裸鼠皮下移植瘤模型,以靶向MDR1基因的siRNA转染荷瘤裸鼠,旨在探讨siRNA在动物体内抑制MDR1基因表达、
出处 《中华妇产科杂志》 CAS CSCD 北大核心 2009年第10期787-789,共3页 Chinese Journal of Obstetrics and Gynecology
基金 基金项目:山东省科学技术发展计划(023130104) 山东省交通科技计划(2005-Y026)
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参考文献12

  • 1Elbashir SM, Harborth J, Lendeckel W, et al. Duplexes of 21- nucleotide RNAs mediate RNA interference in cultured mammalian cells. Nature,2001,411:494-498.
  • 2张晓菁,温泽清,张华玲,石敏.RNA干扰技术抑制耐药细胞MDR1基因表达的研究[J].中国病理生理杂志,2006,22(5):833-836. 被引量:10
  • 3Duan Z, Brakora KA, Seiden MV. Inhibition of ABCB1 (MDR1) and ABCB4 ( MDR3 ) expression by small interfering RNA and reversal of paclitaxel resistance in human ovarian cancer cells. Mol Cancer Ther, 2004,3 : 833-838.
  • 4Markman M. Pharmaceutical management of ovarian cancer: current status. Drugs,2008,68:771-789.
  • 5Sanguino A, Lopez-Berestein G, Sood AK. Strategies for in vivo siRNA delivery in cancer. Mini Rev Med Chem,2008 ,8:248-255.
  • 6Aigner A. Applications of RNA interference: current state and prospects for siRNA-based strategies in vivo. Appl Microbiol Biotechnol, 2007,76 : 9 -21.
  • 7Hua J, Mutch DG, Herzog TJ. Stable suppression of MDR-1 gene using siRNA expression vector to reverse drug resistance in a human uterine sarcoma cell line. Gynecol Oncol,2005,98:31-38.
  • 8刘国艳,瞿全新,糜若然,齐静.RNA干扰技术抑制切除修复交叉互补基因1对卵巢上皮性癌细胞顺铂敏感性的影响[J].中华妇产科杂志,2006,41(5):339-342. 被引量:20
  • 9Hokaiwado N, Takeshita F, Banas A, et al. RNAi-based drug discovery and its application to therapeutics. Idrugs,2008,11: 274-278.
  • 10Hadj-Slimane R, Lepelletier Y, Lopez N, et al. Short interfering RNA (siRNA), a novel therapeutic tool acting on angiogenesis. Biochimie, 2007,89 : 1234- 1244.

二级参考文献14

  • 1张会杰,熊玉卿.P-糖蛋白药物外排作用的研究进展[J].中国临床药理学杂志,2004,20(4):317-320. 被引量:15
  • 2胡海燕,张洹.siRNA对神经胶质瘤细胞株U251 bcl-2基因表达的抑制[J].中国病理生理杂志,2005,21(3):489-493. 被引量:11
  • 3Stein WD. Kinetics of the multidrug transporter (P - glycoprotein) and its reversal[J]. Physiol Rev, 1997, 77(2) : 545 -590.
  • 4Elbashir SM, Harborth J, Lendeckel W, et al. Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells[J]. Nature, 2001, 411(6836) : 428 - 429.
  • 5Duan Z, Brakom KA, Seiden MV. Inhibition of ABCB1(MDR1) and ABCB4 (MDR3) expression by small interfering RNA and reversal of paclitaxel resistance in human ovarian cancer cells[J]. Mol Cancer Ther, 2004, 3(7) : 833 - 838.
  • 6Noonan KE, Beck C, Holzmayer TA, et al. Quantitative analysis of MDRI (multidrug resistance) gene expression in human tumors by polymerase chain reaction[J].Proc Natl Acad Sci USA, 1990, 87(18): 7160-7164.
  • 7Sumimoto H, Yamagata S, Shimizu A, et al. Gene therapy for human small- cell lung carcinoma by inactivation of Skp - 2 with virally mediated RNA interference[J]. Gene Ther, 2005,12(1) : 95 - 100.
  • 8Xu D, Kang H, Fisher M, et al. Strategies for inhibition of MDR1 gene expression[J]. Mol Pharmacol, 2004, 66(2):268 - 275.
  • 9Wood RD.Nucleotide excision repair in mammalian cells.J Biol Chem,1997,272:23465-23468.
  • 10Ferry KV,Hamilton TC,Johnson SW.Increased nucleotide excision repair in cisplatin-resistant ovarian cancer cells:role of ERCC1-XPF.Biochem Pharmacol,2000,60:1305-1313.

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