A fluorescence microplate cytotoxicity assay with a 4-log dynamic range that identifies synergistic drug combinations
| Autor: | Robert T. Proffitt, Tomas Frgala, C. Patrick Reynolds, Ondrej Kalous |
|---|---|
| Rok vydání: | 2007 |
| Předmět: |
Cancer Research
Fenretinide Serial dilution Biology Safingol Neuroblastoma chemistry.chemical_compound Tissue culture Sphingosine Antineoplastic Combined Chemotherapy Protocols Tumor Cells Cultured Humans Enzyme Inhibitors Eosin Y Cytotoxicity Clonogenic assay Buthionine Sulfoximine Melphalan Protein Kinase C Tumor Stem Cell Assay Cell Proliferation Fluorescent Dyes Leukemia Drug Synergism Molecular biology Fluorescence Microscopy Fluorescence Oncology chemistry Eosine Yellowish-(YS) Trypan blue Drug Screening Assays Antitumor |
| Zdroj: | Molecular Cancer Therapeutics. 6:886-897 |
| ISSN: | 1538-8514 1535-7163 |
| DOI: | 10.1158/1535-7163.mct-04-0331 |
| Popis: | Purpose: Cytotoxicity assays in 96-well tissue culture plates allow rapid sample handling for multicondition experiments but have a limited dynamic range. Using DIMSCAN, a fluorescence digital image system for quantifying relative cell numbers in tissue culture plates, we have developed a 96-well cytotoxicity assay with a >4-log dynamic range. Methods: To overcome background fluorescence that limits detection of viable cells with fluorescein diacetate, we used 2′4′5′6′-tetrabromofluorescein (eosin Y) to quench background fluorescence in the medium and in nonviable cells to enhance the reduction of background fluorescence achieved with digital image thresholding. The sensitivity and linearity of the new assay were tested with serial dilutions of neuroblastoma and leukemia cell lines. DIMSCAN was compared with other in vitro cytotoxicity assays: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, colony formation, and trypan blue dye exclusion. Results: Without background fluorescence reduction, scans produced a nearly flat curve across various cell concentrations from 100 to 106 cells per well. Either digital image thresholding or eosin Y dramatically reduced background fluorescence, and combining them achieved a linear correlation (r > 0.9) of relative fluorescence to viable cell number over >4 logs of dynamic range, even in the presence of 4 × 104 nonviable cells per well. Cytotoxicity of deferoxamine for neuroblastoma cell lines measured by the DIMSCAN assay achieved dose-response curves similar to data obtained by manual trypan blue counts or colony formation in soft agar but with a wider dynamic range. Long-term cultures documented the clonogenic ability of viable cells detected by DIMSCAN over the entire dynamic range. The cytotoxicity of two drug combinations (buthionine sulfoximine + melphalan or fenretinide + safingol) was tested using both DIMSCAN and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assays, and the wider dynamic range of DIMSCAN facilitated detection of synergistic interactions. Conclusion: DIMSCAN offers the ability to rapidly and efficiently conduct cytotoxicity assays in 96-well plates with a dynamic range of >4 logs. This assay enables rapid testing of anticancer drug combinations in microplates. [Mol Cancer Ther 2007;6(3):886–97] |
| Databáze: | OpenAIRE |
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