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Effect of IL24 on phosphorylation of eIF2α and proliferation in cancer cells.
Effect of IL24 on phosphorylation of eIF2α and proliferation in cancer cells. A, Melanoma (HO-1, WM35, and MeWo), breast (MCF-7, MDA-MB-231), and cervical cancer cells (HeLa) were treated for 48 hours with Ad.IL24 (100 pfu per cell) or Ad.vector (100 pfu per cell). Cells were collected, protein purified, and subjected to Western blot analysis to detect phospho-eIF2α protein. B, Cells were treated with Ad.IL24 (100 pfu per cell) or Ad.vector (100 pfu per cell), and cell viability was determined by the MTT proliferation assay 5 days after treatment. Numbers represent the ratio of specific treatments to values in control cells (Ad.vector). C, Cells were treated as described in B, and then assayed for cell death using Annexin V staining a measure of apoptosis, and it was determined 48 hours later by FACS analysis using the CellQuest software (Becton Dickinson). An average of three independent experiments is shown ±SD. Leah Persaud et al. Mol Cancer Res 2017;15: ©2017 by American Association for Cancer Research
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