期刊文献+

短发夹状RNA抑制MDR1基因表达逆转卵巢上皮性癌多药耐药的研究

原文传递
导出
摘要 多药耐药性的产生是导致肿瘤化疗失败的重要原因。多药耐药基因MDR1及其所编码的细胞膜P糖蛋白(P-gp)表达增加介导的耐药在化疗中最为主要、最为常见。在过去20多年中,学者们探求各种逆转多药耐药的方法,如反义寡核苷酸技术、核酶技术等,取得了一定的成果。RNA干扰(RNAi)技术抑制MDR1基因表达是研究逆转多药耐药的新途径。本研究设计并构建针对人MDR1基因特定位置的短发夹状RNA(shRNA)质粒pEGFP-H1/MDR1,观察其对卵巢上皮性癌(卵巢癌)紫杉醇耐药细胞株MDR1基因和P-gP表达的抑制作用,探索耐药肿瘤基因治疗的有效方法。
出处 《中华妇产科杂志》 CAS CSCD 北大核心 2007年第4期269-271,共3页 Chinese Journal of Obstetrics and Gynecology
基金 国家自然科学基金(30070786)
  • 相关文献

参考文献7

  • 1栾英姿,李力,黎丹戎,张玮,唐步坚.五种卵巢癌耐药细胞系的建立及其部分耐药相关基因的表达[J].中华妇产科杂志,2004,39(6):403-407. 被引量:21
  • 2Nieth C, Priebsch A, Stege A, et al,Modulation of the classical multidrug resistance (MDR) phenotype by RNA interference (RNAi). FEBS Lett, 2003, 545:144-150.
  • 3Wu H, Hait WN, Yang JM. Small interfering RNA-induced suppression of MDR1 (P-glycoprotein) restores sensitivity to multidrug-resistant cancer cells.Cancer Res, 2003, 63: 1515- 1519.
  • 4Liu R, Hsieh CY, Lam KS. New approaches in identifying drugs to inactivate oncogene products. Semin Cancer Biol, 2004, 14: 13-21.
  • 5Sui G, Soohoo C, Affar el B, et al. A DNA vector based RNAi technology to suppress gene expression in mammalian cells. Proc Natl Acad Sci U S A, 2002, 99:5515-5520.
  • 6Loo TW, Clarke DM. Recent progress in understanding the mechanism of P-glycoprotein-mediated drug efflux. J Membr Biol, 2005,206:173-185.
  • 7Lage H. MDRl/P-glycoprotein (ABCB1) as target for RNA interference-mediated reversal of multidrug resistance. Curr Drug Targets, 2006, 7:813-821.

二级参考文献15

  • 1Webb BL, Lindsay MA, Seybold J, et al. Identification of the protein kinase C isoenzymes in human lung and airways ooth muscle at the protein and mRNA level.Biochem Pharmacol, 1997,54:199-205.
  • 2Withoff S, van der Zee AG, de Jong S, et al. DNA topoisomerase IIalpha and -beta expression in human ovarian cancer.Br J Cancer,1999,79:748-753.
  • 3Fajac A, Da Silva J, Ahomadegbe JC, et al. Cisplatin-induced apoptosis and p53 gene status in a cisplatin-resistant human ovarian carcinoma cell line.Int J Cancer,1996,68:67-74.
  • 4Satoh T, Nishida M, Tsunoda H, et al. Expression of glutathione S-transferase pi (GST-pi) in human malignant ovarian tumors.Eur J Obstet Gynecol Reprod Biol, 2001,96:202-208.
  • 5Hill BT, Moran E, Etievant C, et al. Low-dose twice-daily fractionated X-irradiation of ovarian tumor cells in vitro generates drug-resistant cells overexpressing two multidrug resistance-associated proteins, P-glycoprotein and MRP1.Anticancer Drugs,2000,
  • 6Cvitkovic E. Ongoing and unsaid on oxaliplatin: the hope.Br J Cancer,1998,77 Suppl 4:8-11.
  • 7Perego P, Giarola M, Righetti SC, et al. Association between cisplatin resistance and mutation of p53 gene and reduced bax expression in ovarian carcinoma cell systems.Cancer Res, 1996,56:556-562.
  • 8Asselin E, Mills GB, Tsang BK. XIAP regulates Akt activity and caspase-3-dependent cleavage during cisplatin-induced apoptosis in human ovarian epithelial cancer cells.Cancer Res, 2001,61:1862-1868.
  • 9Cui W, Yazlovitskaya EM, Mayo MS, et al. Cisplatin-induced response of c-jun N-terminal kinase 1 and extracellular signal--regulated protein kinases 1 and 2 in a series of cisplatin-resistant ovarian carcinoma cell lines.Mol Carcinog,2000, 29:219-228.
  • 10Meinhold-Heerlein I, Stenner-Liewen F, Liewen H, et al. Expression and potential role of Fas-associated phosphatase-1 in ovarian cancer.Am J Pathol,2001,158:1335-1344.

共引文献20

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