期刊文献+

人类卵巢癌顺铂耐药细胞株OV1228/cDDP的建立及其生物学特性 被引量:1

Establishment and biological characteristics of cisplatin-resistant cell line OV1228/cDDP of ovarian carcinoma
原文传递
导出
摘要 目的 建立人类卵巢癌细胞顺铂耐药细胞株OV1228/cDDP,并对其生物学特性进行检测.方法 采用顺铂浓度梯度递增法,建立人类卵巢癌顺铂耐药细胞株.通过细胞形态学观察、生长曲线和群体倍增时间测定、药物敏感试验、mdr-1和PKC-α基因及蛋白表达水平的测定,来评价OV1228/cDDP的生物学特性.结果 成功建立了OV1228/cDDP耐药细胞株,耐药指数(RI)为5.97,对多柔比星和5-氟尿嘧啶具有一定的交叉耐药性.与OV1228相比,OV1228/cDDP细胞异型性增加、细胞倍增时间延长 mdr-1和PKC-α在基因和蛋白表达水平均明显增高.结论 OV1228/cDDP细胞对顺铂耐药性稳定,并呈现一定的多药耐药特性,为进一步研究耐药逆转途径提供了实验基础. Objective To establish cisplatin-resistant cell line of human ovarian carcinoma (OV1228/eDDP)and to investigate its biological characteristics.Methods OV1228/cDDP cell line was established by stepwise selection in increasing concentration of cisplatin.Cell morphology,growth curve and population doubling time,mRNA and protein level of mdr-1 and PKC-α were investigated to determine the biological features of OV1228/eDDP cell line.Results The resistant index(RI)of OV1228/cDDP cells was up to 5.97.Cross-resistant of adriamycin(ADM)and 5-Flucytosine(5-Fu)was exhibited.RT-PCR and Western blotting studies showed that the mRNA and protein expression of mdr-1 and PKC-α in the OV1228/cDDP cells were higher than the sensitive cells. Conclusion OV1228/eDDP shows typical multiding resistance phenotypes and might serve as an ideal model for exploring the new route of reversing multidrug resistance.
出处 《肿瘤研究与临床》 CAS 2010年第6期365-367,共3页 Cancer Research and Clinic
基金 江苏省卫生厅面上项目(H200842) 江苏省人事厅“六大人才高峰”项目(08-D-02) 江苏省肿瘤医院重点课题(ZK200701)
关键词 卵巢肿瘤 顺铂 多药耐药 细胞株 Ovarian neoplasms Cisplatin Drug resistance Cell line
  • 相关文献

参考文献8

  • 1Nardi M,De Marco S,Fabi A,et al.Cisplatin and escalating doses of paclitaxel and epirubicin in advanced ovarian cancer.CCP,2001,48:255-258.
  • 2Takara K Sakaeda T,Okumura K.An update on overcoming MDR1-mediated multidrug resistance in eancer chemotherapy.Curr Pharm Design,2006,12:273-286.
  • 3王金华,赵万洲,陈小祥,赵一兵,曲军卫,彭素蓉.人卵巢癌细胞系OV1228的建立及其生物学特性[J].中国肿瘤外科杂志,2009,1(5):281-284. 被引量:2
  • 4韩丽妹,潘弘,方晓玲.人卵巢癌紫杉醇耐药细胞株的建立和生物学特性评价[J].复旦学报(医学版),2008,35(2):171-175. 被引量:4
  • 5Ozds RF,Odwayer PJ,Hamilton TC.Clinical reversal of drug resistance in ovarian cancer.Cancer,1993.51:90.
  • 6周友珍,陈惠祯,杨庆忆,刘诗权,侯汉英.人卵巢癌顺铂耐药细胞株的建立及其耐药机制的研究[J].中华医学杂志,1996,76(9):680-683. 被引量:27
  • 7Li L,Luan Y,Wang G,et al.Development and characterization of five cell models for chemoresistance studies of human ovarian carcinoma.Int J Mol Med,2004,14:257-264.
  • 8Gill PK.Gescher A,Gant TW.Regulation of MDR1 promoter activity in human breast carcinoma cells by protein kinase cisozymes alpha and theta.Eur J Biochem,2001.268:4151-4157.

二级参考文献22

共引文献29

同被引文献14

  • 1孙鹏达,谷洋,王庆国.大肠癌新辅助化疗[J].国际肿瘤学杂志,2006,33(2):151-153. 被引量:10
  • 2Shih IM, Wang TL. Notch signaling, γ-secretase inhibitors, and cancer therapy [J]. Cancer Res, 2007, 67 (5): 1879-1882.
  • 3Qiao L, Wong BC. Role of Notch signaling in colorectal cancer [J]. Carcinogenesis, 2009, 30 (12): 1979-1986.
  • 4Lee TJ, Kim EJ, Kim S, et aL Caspase-dependent and caspase- independent apoptosis induced by evodiamine in human leukemic U937 cells [J]. Mol Cancer Ther, 2006, 9 (5): 2398-2407.
  • 5Konishi J, Kawaguchi KS, Huan V, et al. γ-Secretase inhibitor prevents Notch3 activation and reduces proliferation in human lung cancers [J]. Cancer Res, 2007, 67 (17): 8051-8057.
  • 6S arkadi B, Homolya L, Szakacs G, et al. Human multidrug resistance ABCB and ABCG transporters: participation in a chemoimmunity defense system [J]. Physiol Rev, 2006, 86 (4): 1179-1236.
  • 7Thomas H, Coley HM. Overcoming multidrug resistance in cancer: an update on the clinical strategy of'inhibiting p- glyeoprotein [J]. Cancer Control, 2003, 10 (2): 159-165.
  • 8Mishima K, Nariai Y, Yoshimura Y. Etodolac, a selective cyclo- oxygenase-2 inhibitor, enhances carboplatin-induced apoptosis of human tongue carcinoma cells by down-regulation of FAP-1 expression [J]. Oral Oncol, 2005, 41 (1): 77-81.
  • 9Zhu YM, Zhao WL, Fu JF, et al. NOTCH1 mutations in T-cell acute lymphoblastic leukemia: prognostic significance and implication in muhifactorial leukemogenesis [J]. Clin Cancer Res, 2006, 12 (10): 3043-3049.
  • 10Zhang Y, Wang Z, Ahmed F, et al. Down-regulation of Jagged-1 induces cell growth inhibition and S phase arrest in prostate cancer cells [J]. Int J Cancer, 2006, 119 (9): 2071-2077.

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