期刊文献+

丝裂霉素C的给药间隔与膀胱癌细胞耐药性的研究 被引量:1

Study of intervals of mitomycin C treatment and the mutildrug resistance of bladder cancer
下载PDF
导出
摘要 目的研究丝裂霉素C(MMC)的给药间隔与膀胱移行细胞癌多药耐药之间的关系及机制。方法分别间隔24、48、72和96小时,用MMC处理膀胱移行细胞癌BIU87细胞株2个小时,共5次,用MTT法检测细胞毒作用,Westernblot分析p170和p53的表达。结果①MMC首次处理BIU87、间隔24、48、72和96小时给药的IC50分别为4.41、0.71、2.83、4.51及6.16μg/ml;②间隔24小时给药,p53显著下调,未检测到p170表达,间隔48、72、96小时给药,p53持续表达,p170的表达逐渐增强。结论膀胱癌细胞的耐药性与丝裂霉素C的给药间隔密切相关,其机制可能与p53表达的变化有关。 Objective To study the relationship between the intervals of mitomycin C treatment and the mutildrug resistance of bladder transitional cell cancer line and its mechanism.Methods The bladder transitional cell cancer line BIU-87 was treated with mitomycin C two hours every time for five times with intervals of 24,48,72 and 96 hours respectively.Cystotoxicity was measured by MTT and p53 and p170 expression were analyzed by Western blot.Results ①The IC_50(μg/ml)were 4.41,0.71,2.83,4.51and 6.16 respectively of the first time treatment,treatment after 24,48,72 and 96 hours.②p53 was significantly down-regulated while p170 was not detected at 24 hours interval treatment.p53 continuously expressed and p170 increasingly expressed at 24,48,72 and 96 hours intervals treatment.Conclusion The mutildrug resistance of bladder cancer cell was closely related with the treatment intervals of mitomycin C,which maybe correlated with p53 expression.
出处 《癌症进展》 2005年第5期490-493,共4页 Oncology Progress
关键词 膀胱移行细胞癌 多药耐药性 丝裂霉素C bladder transitional cell cancer mutildrug resistance mitomycin C
  • 相关文献

参考文献5

  • 1[1]Bosch I, Croop J. P-glycoprotein multidrug resistance and cancer. Biochim Biophys Acta, 1996, 9:1288
  • 2周兴,刘春晓,郑少波,梅骅,郑克立,秦自科.膀胱癌mdr-1 mRNA表达水平及临床意义[J].中华泌尿外科杂志,1999,20(2):86-87. 被引量:4
  • 3[3]Chin KV, Ueda K, Pastan I, et al. Modulation of activity of the promoter of the human MDR1 gene by Ras and p53. Science, 1992, 255 (5043):459
  • 4[4]Kopnin BP, Stromskaya TP, Kondratov RV, et al. Influence of exogenous ras and p53 on P-glycoprotein function in immortalized rodent fibroblasts. Oncol Res, 1995, 7:299
  • 5[5]Smith ND, Rubenstein JN, Eggener SE, et al. The p53 tumor suppressor gene and nuclear protein: Basic science review and relevance in the management of bladder cancer. J Urol, 2003,169 (4): 1219

二级参考文献2

  • 1Her H W,中华肿瘤杂志,1995年,13卷,1404页
  • 2梅骅,中华泌尿外科杂志,1990年,11卷,34页

共引文献3

同被引文献18

  • 1李涛,陈梓甫,林成栋,高祥勋,何延瑜,张延榕.尿细胞角蛋白对膀胱癌术后复发的监测价值[J].临床泌尿外科杂志,2004,19(10):594-596. 被引量:1
  • 2崔曙,唐铁龙,李响,李虹.nm23-H1基因转染对膀胱癌T-24细胞转移能力及化疗敏感性的影响[J].四川大学学报(医学版),2007,38(5):788-791. 被引量:2
  • 3Gndfroid E,Geuskem M,Dupressuir Tet al.Cytokeratins M exposed on the outer surface of established human mammary carcinoma ceUs. Journal of Cell Science . 1991
  • 4Chu YW,Runyan RB,Oshima RGet al.Expression of complete keratin filaments in mouse L cells augments cell migration and invasion. Proceedings of the National Academy of Sciences of the United States of America . 1993
  • 5Schaafsma HE,Ramaekers FCS,Van Muijen GNPet al.Cytokeratin expression patterns in metastatic transitional cell carcinoma of the urinary tract. American Journal of Pathology . 1991
  • 6Masayuki Kamada,Mototsugu muramaki,Palma Rocchi,et al.Hsp27 knockdown using nucleotide-based therapies inhibit tumor growth and enhance chemotherapy in human bladder cancer cells. Molecular Cancer Therapeutics . 2007
  • 7Gires O,Andratschke M,Schmitt B, et al.Cytokeratin 8 associates with the external leaflet of plasma membranes in tumour cells. Biochemical and Biophysical Research Communications . 2005
  • 8Obermajer N,Doljak B,Kos J.Cytokeratin 8 ectoplasmic domain binds urokinase-type plasminogen activator to breast tumor cells and modulates their adhesion growth and invasiveness. Molecular Cancer . 2009
  • 9Samali A,Robertson JD,Peterson E,et al.Hsp27 protects mitochondria of thermotolerant cells against apoptotic stimuli. Cell Stress and Chaperones . 2001
  • 10Gilles AM,Presecan E,Vonica A,et al.Nucleoside diphosphate kinase from human erythrocytes: structural characterization of the two polypeptide chains responside for heterogeneity of the hexameric enzyme. Journal of Biological Chemistry . 1991

引证文献1

二级引证文献3

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