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WP631, a new DNA-binding drug that bisintercalates into DNA with high affinity, seems to be highly cytotoxic against Jurkat T lymphocytes. The purpose of this study was to gain new insights into the mechanisms by which WP631 halts proliferation in this cell type. Treating Jurkat cells with nanomolar concentrations of WP631 produced G(2)/M arrest, inhibited the transcription of c-myc and p53 genes, and induced limited apoptosis during the duration of treatment. Suppression of c-myc and p53 expression, and time-dependent decline in c-Myc and p53 protein levels, was associated with growth arrest. A weak interdependence was also found between the potent antiproliferative activity and the apoptotic response; treatment with WP631 for 24-36hr produced arrest in G(2)/M and allowed for partial DNA repair. Longer treatments with WP631 allowed some repaired cells to re-enter the cell cycle, but produced aneuploidy or apoptosis in others.
G2 Phase, Transcription, Genetic, Daunorubicin, Mitosis, Intercalating Agents, Proto-Oncogene Proteins c-myc, Jurkat Cells, T-Lymphocyte Subsets, Tumor Cells, Cultured, Humans, Tumor Suppressor Protein p53
G2 Phase, Transcription, Genetic, Daunorubicin, Mitosis, Intercalating Agents, Proto-Oncogene Proteins c-myc, Jurkat Cells, T-Lymphocyte Subsets, Tumor Cells, Cultured, Humans, Tumor Suppressor Protein p53
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| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
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