Orlandi L, Zaffaroni N, Bearzatto A, Silvestrini R
Divisione di Oncologia Sperimentale C, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy.
Br J Cancer. 1996 Dec;74(12):1924-8. doi: 10.1038/bjc.1996.654.
We previously reported that combined treatment with melphalan and mild hyperthermia (1 h at 42 degrees C) caused a synergistic cytotoxic effect in JR8 melanoma cells, paralleled by a stabilisation of a melphalan-induced G2-phase cell block. In this study, we investigated the effect of melphalan and hyperthermia on proteins that regulate G2-M transition. Neither hyperthermia nor melphalan at a concentration of 2.5 micrograms ml-1, which had no antiproliferative effect at 37 degrees C, interfered with cyclin B1 expression or p34cdc2 kinase activity. At a concentration of 8.5 micrograms ml-1, which reduced cell growth by 50% at 37 degrees C, melphalan inhibited p34cdc2 kinase activity as a consequence of an increased tyrosine phosphorylation of the protein. A similar inhibitory effect on p34cdc2 kinase was obtained when the lowest melphalan concentration (2.5 micrograms ml-1) was used under hyperthermic conditions. Our results indicate that thermal enhancement of melphalan cytotoxicity could be mediated at least in part by an inhibition of p34cdc2 kinase activity, which prevents cell progression into mitosis.
我们之前报道过,美法仑与轻度热疗(42摄氏度,1小时)联合治疗在JR8黑色素瘤细胞中产生了协同细胞毒性作用,同时美法仑诱导的G2期细胞阻滞得到了稳定。在本研究中,我们研究了美法仑和热疗对调节G2-M期转换的蛋白质的影响。浓度为2.5微克/毫升的热疗或美法仑在37摄氏度时无抗增殖作用,它们均未干扰细胞周期蛋白B1的表达或p34cdc2激酶活性。在浓度为8.5微克/毫升时,美法仑在37摄氏度下使细胞生长减少50%,该浓度的美法仑由于蛋白质酪氨酸磷酸化增加而抑制p34cdc2激酶活性。当在热疗条件下使用最低美法仑浓度(2.5微克/毫升)时,对p34cdc2激酶也获得了类似的抑制作用。我们的结果表明,美法仑细胞毒性的热增强作用至少部分可能是由对p34cdc2激酶活性的抑制介导的,该抑制作用阻止细胞进入有丝分裂。