β Scribed by Coffey, Dennis C. ;Kutko, Martha C. ;Glick, Richard D. ;Swendeman, Steven L. ;Butler, Lisa ;Rifkind, Richard ;Marks, Paul A. ;Richon, Victoria M. ;LaQuaglia, Michael P.
No coin nor oath required. For personal study only.
Neuroblastoma is a common childhood cancer with a poor overall prognosis. retinoic acids (ras) have been studied as a potential therapy, showing promise in recurrent disease. the histone deacetylase inhibitor (hdaci) m-carboxycinnamic acid bishydroxamide (cbha) is another potential therapy, which we recently described. combinations of ras and hdacis currently under investigation display synergy in certain neoplasms. in this study, we evaluate the effect of combinations of ras and hdacis on human neuroblastoma cells.
Established cell lines were cultured in increasing concentrations of hdacis, ras, and combinations thereof. following exposure, viable cell number was quantified by trypan blue dye exclusion on a hemacytometer. cell cycle analysis was performed by propidium iodide staining and facs.
All assayed hdacis and ras decreased viable cell number. lower concentrations of each agent were effective when the two were combined. the primary reason for decreased cell number appears to be apoptosis following hdaci exposure and g1 arrest following ra exposure. both effects are seen with cotreatment. caspase inhibition abrogates the apoptotic response.
Cbha causes apoptosis of human neuroblastoma in vitro, an effect that can add to the effects of ra. hdacis and ras inhibit neuroblastoma in significantly lower concentrations when used together than when used individually. combination therapy may improve the ultimate efficacy while reducing the side effects of these agents in clinical use.
π SIMILAR VOLUMES
Farnesyltransferase catalyzes the posttranslational modification of numerous proteins involved in intracellular signal transduction by transferring the farnesyl residue of farnesyl pyrophosphate to the thiol of a cysteine side chain of the protein substrate. The cysteine residue belongs to a charact
To examine the role of protein kinase A (EC 2.7.1.37) isozymes in the retinoic acid-induced growth inhibition and neuronal differentiation, we investigated the changes of protein kinase A isozyme patterns in retinoic acid-treated SH-SY5Y human neuroblastoma cells. Retinoic acid induced growth inhibi