期刊文献+

乳腺癌多药抗药相关药物的体外敏感性与mdr-1基因表达 被引量:2

The relationship between in vitro chemosensitivity of human breast cancer to MDR related drugs and expression of mdr 1 gene
原文传递
导出
摘要 探讨乳腺癌多药抗药(MDR)相关药物的体外敏感性与mdr-1基因表达的关系,为乳腺癌的合理化疗提供理论依据。方法采用体外MTT药敏试验及多聚酶链反应(RT-PCR)技术,检测了56例乳腺癌病人的原代乳腺癌细胞对MDR相关药物的敏感性,及乳腺癌组织的mdr-1基因表达水平。结果体外抗药乳腺癌的mdr-1基因阳性表达率均明显升高;Imax%与mdr-1基因表达水平无关;而IC50与mdr-1基因性的相关性具有统计学意义。 Objective To study the relationship between in vitro chemosensitivity of human breast cancer to MDR related drugs and experssion of mdr 1 gene.Methods We measured the chemosensitivity of 56 human breast cancers to MDR related drugs by MTT assay in vitro and level of mdr 1mRNA in these samples by RT PCR technique.Results The expression of mdr 1gene in the breast cancer resistant to drugs in vitro was increased significantly.The level of mdr 1mRNA was not correlated with I max %,but correlated with IC50 statistically.Conclusion These results support that the increased expression of mdr 1 gene is a major cause of resistance to MDR related drugs.
出处 《中华医学杂志》 CAS CSCD 北大核心 1997年第5期371-373,共3页 National Medical Journal of China
关键词 乳腺肿瘤 MDR-1 基因表达 聚合酶链反应 抗药性 Breast neoplasma Drug tolerance MTT Colorimetry gene Expression Polymerase chain reaction
  • 相关文献

参考文献3

  • 1刘晓晴,中华肿瘤杂志,1997年,19卷,1页
  • 2刘晓晴,中华肿瘤杂志,1996年,18卷,263页
  • 3徐建明,中华肿瘤杂志,1995年,17卷,100页

同被引文献12

  • 1徐建明,汤仲明,宋三泰,江泽飞,李家益,杨奕静.人乳腺癌原代培养体外药敏试验的评价[J].中华肿瘤杂志,1995,17(2):100-103. 被引量:22
  • 2刘晓晴,石成华,宋三泰,张京生,徐建明,汤仲明,江泽飞.RT-PCR方法检测临床乳癌组织的多药耐药基因表达[J].中华肿瘤杂志,1996,18(4):263-265. 被引量:12
  • 3[2]Juliano RL, Ling V. A surface glycoprotein modulating drug permeability in chinese hamster ovary cell mutants[J]. Biochem Biophys Acta, 1976,455(1):152~162
  • 4[3]Chen CJ, Chin JE, Ueda K, et al. Internal duplication and homology with bacterial transport proteins in the MDR-1 gene from MDR human cells[J]. Cell, 1986, 47(3):381~389
  • 5[5]Raaijmakers HGP, Izquierdo MAI, Lokhorst HM, et al. Lung-resistance related protein expression is anegative predictive factor for response to conventional low but not to intensified dose alkylating chemotherapy in multiple myeloma [J]. Blood, 1998, 91 (3):1029 ~ 1036
  • 6[7]Frei E Ⅲ, Antman K, Teicher B, et al. Bone marrow autotransplantatinon for solid tumors-prospects [J]. J Clin Oncol, 1989, 7(4):515~526
  • 7[8]Codman AJ, godie JH. Impact of dose-intense chemotherapy on the development of permanent drug resistance [J]. Semin Oncol,1987, 14(4 Suppl 4):29~33
  • 8[9]Peters WP, Ross M, Vredenburgh JJ, et al. High-dose chemotherapy and autlogous bone morrow support as consolidation after standard-dose adjuvant therapy for high risk prmiary breastcancer[J].J Clin Oncol, 1993, 11(6):1132~1143
  • 9[10]Venturini M, Mastro LD, Melioli G, et al. Release of peripheral blood stem cells during standard dose cyclophosphamide,epidoxorublcin 5-fluorouracil regimen plus granulocyte coony-stmiulating factor for breast cancer therapy[J]. Cancer, 1994, 74(8):2300~2306
  • 10徐建明,宋三泰,汤仲明,江泽飞,周莉,刘晓晴,李彦博,杨奕静.MTT体外药敏试验指导下的乳癌预见性化疗[J].中华肿瘤杂志,1997,19(2):153-156. 被引量:43

引证文献2

二级引证文献5

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