Induction of apoptosis by NS398.

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Induction of apoptosis by NS398. Induction of apoptosis by NS398. A, DNA fragmentation assay. Colon cancer cells were treated with DMSO (control) or 100 μm NS398 for 2 days. Both floating and adherent cells were collected, and soluble DNA from each cell fraction was extracted and electrophoresed on a 1.8% agarose gel. The gels were stained with ethidium bromide and photographed. The experiments were repeated once. B, TUNEL assay. Cells were treated with DMSO (control) or 100 μm NS398 for 2 days. Both floating and adherent cells were collected, labeled with BrdUrd, and stained with propidium iodide. The cells were then analyzed by flow cytometry using a FACScan flow cytometer. The experiments were repeated once. Ming Li et al. Clin Cancer Res 2001;7:1010-1016 ©2001 by American Association for Cancer Research