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Effect of Extracellular ATP on Cisplatin-Induced Cytotoxicity in Human Ovarian Carcinoma Cells
被引:8
|作者:
Rotte, Anand
[1
]
Garmann, Dirk
[1
]
Buss, Irina
[1
]
Jaehde, Ulrich
[1
]
机构:
[1] Univ Bonn, Dept Clin Pharm, Inst Pharm, DE-53121 Bonn, Germany
关键词:
ATP;
Cancer;
Cisplatin;
Cytotoxicity;
COPPER TRANSPORTER CTR1;
GROWTH-INHIBITION;
LEUKEMIA-CELLS;
CANCER-CELLS;
ADENOSINE-TRIPHOSPHATE;
PASSIVE PERMEABILITY;
EXTERNAL ATP;
TUMOR-CELLS;
RESISTANCE;
INVOLVEMENT;
D O I:
10.1159/000287351
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Background: Cisplatin resistance has been mainly associated with decreased cellular accumulation and increased intracellular glutathione (GSH) levels. ATP is known to increase the membrane permeability of cells and to decrease intracellular GSH levels. Our study aimed at using extracellular ATP to sensitize ovarian carcinoma cells towards cisplatin. Methods: The MTT assay was used to determine the EC50 of cisplatin in the human ovarian carcinoma cell line A2780 and its cisplatin-resistant variant A2780cis. Intracellular platinum concentrations were determined using flameless atomic absorption spectrometry. Results: Preincubation and concomitant incubation with ATP did not alter the EC50 of cisplatin. The presence of 100 mu M ATP along with cisplatin decreased cell survival in A2780 but not in A2780cis cells. Extracellular ATP did not increase the cellular accumulation of cisplatin in both A2780 and A2780cis cells. Conclusion: The presence of extracellular ATP during treatment with cisplatin leads to additive cytotoxicity in the sensitive A2780 but not in cisplatin-resistant A2780cis cells. Copyright (C) 2010 S. Karger AG, Basel
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页码:1 / 8
页数:8
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