Bryostatin 1-tamoxifen combinations show synergistic effects on the inhibition of growth of P388 cells in vitro.
dc.contributor.author | McGown, Alan T | |
dc.contributor.author | Jayson, Gordon C | |
dc.contributor.author | Pettit, G R | |
dc.contributor.author | Haran, M S | |
dc.contributor.author | Ward, Timothy H | |
dc.contributor.author | Crowther, Derek | |
dc.date.accessioned | 2010-02-12T15:51:41Z | |
dc.date.available | 2010-02-12T15:51:41Z | |
dc.date.issued | 1998 | |
dc.identifier.citation | Bryostatin 1-tamoxifen combinations show synergistic effects on the inhibition of growth of P388 cells in vitro. 1998, 77 (2):216-20 Br. J. Cancer | en |
dc.identifier.issn | 0007-0920 | |
dc.identifier.pmid | 9460991 | |
dc.identifier.uri | http://hdl.handle.net/10541/92029 | |
dc.description.abstract | This study shows that combinations of bryostatin 1, a novel modulator of protein kinase C currently under clinical evaluation, with the anti-oestrogenic agent tamoxifen caused a large synergistic enhancement of growth inhibition in P388 cells in vitro. The growth-inhibitory effects of bryostatin 1 in the presence of non-inhibitory concentrations of tamoxifen were increased by approximately 200-fold, whereas growth inhibition by tamoxifen in the presence of non-inhibitory concentrations of bryostatin 1 were increased over 30-fold. These data have been confirmed by isobologram analysis. The precise mechanism underlying this effect is unknown, although preliminary data implicating protein kinase C is presented. The magnitude of this synergistic effect, together with evidence of clinical responses seen when these agents were given sequentially in ovarian cancer, merits further study. | |
dc.language.iso | en | en |
dc.subject | Leukaemia P388 | en |
dc.subject.mesh | Animals | |
dc.subject.mesh | Bryostatins | |
dc.subject.mesh | Cell Division | |
dc.subject.mesh | Drug Synergism | |
dc.subject.mesh | Enzyme Activation | |
dc.subject.mesh | Growth Inhibitors | |
dc.subject.mesh | Lactones | |
dc.subject.mesh | Leukemia P388 | |
dc.subject.mesh | Macrolides | |
dc.subject.mesh | Mice | |
dc.subject.mesh | Protein Kinase C | |
dc.subject.mesh | Staurosporine | |
dc.subject.mesh | Tamoxifen | |
dc.subject.mesh | Tetradecanoylphorbol Acetate | |
dc.title | Bryostatin 1-tamoxifen combinations show synergistic effects on the inhibition of growth of P388 cells in vitro. | en |
dc.type | Article | en |
dc.contributor.department | Paterson Institute for Cancer Research, Christie Hospital NHS Trust, Manchester, UK. | en |
dc.identifier.journal | British Journal of Cancer | en |
html.description.abstract | This study shows that combinations of bryostatin 1, a novel modulator of protein kinase C currently under clinical evaluation, with the anti-oestrogenic agent tamoxifen caused a large synergistic enhancement of growth inhibition in P388 cells in vitro. The growth-inhibitory effects of bryostatin 1 in the presence of non-inhibitory concentrations of tamoxifen were increased by approximately 200-fold, whereas growth inhibition by tamoxifen in the presence of non-inhibitory concentrations of bryostatin 1 were increased over 30-fold. These data have been confirmed by isobologram analysis. The precise mechanism underlying this effect is unknown, although preliminary data implicating protein kinase C is presented. The magnitude of this synergistic effect, together with evidence of clinical responses seen when these agents were given sequentially in ovarian cancer, merits further study. |