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基因mdr1高表达多药耐药肿瘤细胞对力达霉素的药物敏感性
引用本文:师以康,吴淑英,黄云虹,甄永苏. 基因mdr1高表达多药耐药肿瘤细胞对力达霉素的药物敏感性[J]. 药学学报, 2006, 41(12): 1146-1151
作者姓名:师以康  吴淑英  黄云虹  甄永苏
作者单位:中国医学科学院、中国协和医科大学,医药生物技术研究所,北京,100050
基金项目:国家高技术研究发展计划(863计划)
摘    要:目的利用经药物诱导获得的mdr1基因高表达细胞株以及通过mdr1基因转染建立的稳定高表达细胞株,研究多药耐药肿瘤细胞对力达霉素(C-1027)的药物敏感性。方法构建mdr1重组真核表达质粒pcDNA3.1/mdr1,利用脂质体转染技术,获得mdr1高表达HepG2肝癌细胞。经RT-PCR、细胞荧光免疫化学及罗丹明外排实验,鉴定了细胞的mdr1表达水平和药物外排活性。MTT方法测定敏感细胞及相对应的多药耐药细胞对力达霉素等多种抗肿瘤药物的药物敏感性。结果mdr1稳定转染细胞株HepG2/mdr1、多药耐药KBv200细胞和MCF-7/ADR细胞对力达霉素的IC50值分别为(0.020±0.011) nmol·L-1,(0.24±0.20) nmol·L-1和(0.028±0.011) nmol·L-1。相对于各自的敏感细胞,多药耐药细胞HepG2/mdr1,KBv200和MCF-7/ADR对力达霉素的抗药倍数分别是1.3,6.8和1.6倍,对阿霉素的抗药倍数分别是8.8, 37.2和181.3倍,对紫杉醇的抗药倍数分别是40.3, 336.8和49.2倍。结论 mdr1高表达的多药耐药肿瘤细胞对力达霉素仍高度敏感,未表现出抗药性。

关 键 词:多药耐药性  力达霉素  mdr1基因  P-糖蛋白
文章编号:0513-4870(2006)12-1146-06
收稿时间:2006-02-20
修稿时间:2006-02-20

Chemosensitivity of mdr1 gene overexpressed multidrug resistant cancer cells to lidamycin
SHI Yi-kang,WU Shu-ying,HUANG Yun-hong,ZHEN Yong-su. Chemosensitivity of mdr1 gene overexpressed multidrug resistant cancer cells to lidamycin[J]. Acta pharmaceutica Sinica, 2006, 41(12): 1146-1151
Authors:SHI Yi-kang  WU Shu-ying  HUANG Yun-hong  ZHEN Yong-su
Affiliation:Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
Abstract:AIM: To investigate the chemosensitivity to lidamycin (C-1027) in mdr1 gene overexpressing cancer cell lines established by drug induction and by gene-transfection. METHODS: DNA was cloned by RT-PCR and then eukaryotic expressing recombinant plasmid pcDNA3. 1/mdrl was constructed. Using Lipofectamine 2000, a strain of stably transfected human hepatoma cancer cells, HepG2/mdrl, was obtained. The mdr1 mRNA level, P-glycoprotein (P-gp) level and the activity of P-gp to extrude drugs in cancer cells were determined by RT-PCR, immunofluorescence analysis and rhodamine 123 efflux assay. The chemosensitivity of cancer cells with low or high mdr1 expression to lidamycin and other antitumor drugs was tested by MTT assay. RESULTS: The mdr1 mRNA and P-gp levels in KBv200, MCF-7/ADR, and stably transfected HepG2/mdr1 cells were much higher than that in respective parent KB, MCF-7 and HepG2 cells. The IC50 values of lidamycin for KBv200, MCF-7/ADR and HepG2/mdrl cells were (0.24 +/- 0.20) nmol x L(-1), (0.028 +/- 0.011) nmol x L(-1), and (0.020 +/- 0.011) nmol x L(-1), respectively. Compared with parental cells, the values of resistant fold for KBv200, MCF-7/ADR and HepG2/mdr1 cells to lidamycin were 6.8, 1.6 and 1.3 fold; to adriamycin were 37.2, 181.3 and 8.8 fold; to taxol were 336.8, 49.2 and 40.3 fold, respectively. CONCLUSION: Lidamycin is highly active to multidrug resistant cancer cells. The chemosensitivity of those resistant cancer cells to lidamycin is approximately at the similar level as that of parent cancer cells.
Keywords:multiple drug resistance   lidamycin   mdrl gene    P-glycoprotein
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