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重组人血管内皮抑素逆转人肺腺癌A549/DDP细胞耐药性研究 被引量:2

Reversal effect of recombinant human Endostatin on cisplatin resistance line A549/DDP human lung adenocarcinoma cells
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摘要 目的探讨重组人血管内皮抑素(rh-ES)对A549/DDP细胞耐药性的逆转作用。方法采用人肺腺癌细胞株A549及耐药细胞株A549/DDP作为研究对象,以顺铂(DDP)与重组人血管内皮抑素两者联合及单独给药的方式分别作用于人肺腺癌细胞株A549及耐药细胞株A549/DDP,作用时间72h,观察不同给药方式造成的同株细胞之间耐药性的不同及不同株细胞间耐药性的差别,采用四甲基偶氮唑蓝(MTT)检测重组人血管内皮抑素对A549/DDP细胞耐药性的逆转作用。结果DDP对A549细胞半数抑制浓度(IC50)为(0.72±0.05)μg/ml,对A549/DDP的IC50为(11.54±0.64)μg/ml。rh-Es联合DDP对A549/DDP的IC50为(2.0±0.1)μg/ml。逆转倍数(RF)为5.77,相对逆转率(RRR)为88.2%。结论重组人血管内皮抑素能逆转A549/DDP对DDP的耐药性。 Objective To evaluate reverse effect of recombinant human Endostatin on drug-resistance of A549/DDP cells to cisplatin (DDP). Methods Lung adenocarcinoma cell line 3.549 and its DDP-resistant cell line A549/DDP were treated with DDP and recombinant human Endostatin. Difference in drug resistance was analyzed between different regimens (DDP, Endostatin and combination) and between different cell lines (human lung adenocarcinoma A549 and drug resistant A549/DDP), after a 72h-treatment in vitro. Recerse effect of recombinant human Endostatin on drug-resistance of A549/DDP to DDP was tested by MTT assay. Results The observed 50% inhibitory concentration (IC50) was (0. 72±0. 05) ug/ml against A549 and (11.54± 0.64)against A549/DDP in DDP, and (2.0±0.1 )μg/ml against A549/DDP in rh-Endostatin-DDP combination respectively, with a reversal fold (RF) of 5.77 and a relative reversal rate of 88. 2%. Conclusion rh-Endostatin may reverse drug-resistance of A549/DDP cells to DDP.
出处 《国际肿瘤学杂志》 CAS 2010年第7期550-554,共5页 Journal of International Oncology
基金 大连市科技厅课题资助项目(2007E21SF260)
关键词 内皮抑素类 肺肿瘤 抗药性 肿瘤 A549/DDP细胞株 Endostatins Lung neoplasms Drug resistance, neoplasms A549/DDP cell line
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  • 1蔡鹏,刘叙仪,韩复生,王萍.耐顺铂人肺腺癌细胞系A_(549)DDP的建立及耐药机制[J].中国肿瘤临床,1995,22(8):582-587. 被引量:29
  • 2刘梅梅,隋丽华,李佩玲,程丽.Endostatin抑制人卵巢癌细胞生长及其在裸鼠皮下移植瘤中的作用[J].第四军医大学学报,2006,27(3):282-284. 被引量:4
  • 3沈惠麒 赵利英.组织中谷胱甘肽的荧光测定法[J].中华劳动卫生职业病杂志,1988,6:103-108.
  • 4Bischoff JR, Kirn DH, Williams A, et al. An adenovirus mutant that replicates selectively in p53-deficient human tumor cells [J]. Science, 1996,274(5286): 373-376.
  • 5Ganly I, Kim YT, Hann B, et al. Replication and cytolysis of an E1B-attenuated adenovirus in drug-resistant ovarian tumour cells is associated with reduced apoptosis [J]. Gene Ther,2001,8(5) :369-375.
  • 6Heise C, Lemmon M, Kim D. Efficacy with a replicationselective adenovirus plus cisplatin-based chemotherapy:dependence on sequencing but not p53 functional status or route of administration [J]. Clin Cancer Res, 2000,6(12):4908-4914.
  • 7Rogulski KR, Freytag SO, Zhang K, et al. In vivo antitumor activity of ONYX-015 is influenced by p53 status and is augmented by radiotherapy [J]. Cancer Res, 2000,60(5):1193-1196.
  • 8Ferguson PJ. Mechanisms of resistance of human tumours to anticancer drugs of the platinum family: a review [J]. J Otolaryngol, 1995,24(4) :242-252.
  • 9Kuo MT, Bao J, Furuichi M, et al. Frequent coexpression of MRP1/GS-X pump and gamma-glutamylcysteine synthetase mRNA in drug-resistant cells, untreated tumor cells, and normal mouse tissues [J]. Biochem Pharmacol, 1998,55(5):605-615.
  • 10Nevins J. Adenovirus E1A-dependent transactivation of transcription [J]. Cancer Biol, 1990,1 ( 1 ): 59-67.

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