Division of Medical Oncology, Tulay Aktas Oncology Hospital, School of Medicine, Ege University, Bornova, Izmir, Turkey.
Mol Biol Rep. 2011 Jan;38(1):249-59. doi: 10.1007/s11033-010-0102-6. Epub 2010 Mar 28.
We report that all-trans retinoic acid (ATRA) in combination with zoledronic acid has strong synergistic cytotoxic and apoptotic effects against human hormone- and drug-refractory prostate cancer cells, PC-3 and DU-145, in a time- and dose-dependent manner. We further investigated the effect of the combination treatment on the apoptotic process by both oligoarray and protein array analysis in DU-145 cells, in which the drug combination shows much more strong synergistic effects, as compared to PC-3 cells. Moreover, we have also performed real time-PCR array analysis to validate oligoarray results. We demonstrated that the combination of ATRA and zoledronic acid is a strong inducer of apoptotic related cell death in human androgen-and drug refractory prostate cancer cells DU-145, at either transcriptional or translational levels. While expression of proapoptotic genes such as tumor necrosis factor receptor superfamily (TNFRSF), Bad, Bax, Fas, FADD are induced with the exposure of the combination, expression of antiapoptotic genes or proteins such as members of inhibitor apoptosis family (IAPs), MCL-1, LTBR, p53 and bcl-2 are reduced. Because this novel combination treatment has fewer side effects than is generally the case with conventional cytotoxic agents, this regimen may be a good option for treatment of elderly prostate cancer patients.
我们报告称,全反式维甲酸(ATRA)与唑来膦酸联合使用对人激素和药物难治性前列腺癌细胞 PC-3 和 DU-145 具有强烈的协同细胞毒性和凋亡作用,这种作用具有时间和剂量依赖性。我们通过 DU-145 细胞中的寡核苷酸和蛋白质阵列分析进一步研究了联合治疗对凋亡过程的影响,结果表明与 PC-3 细胞相比,该药物联合具有更强的协同作用。此外,我们还进行了实时 PCR 阵列分析以验证寡核苷酸阵列结果。我们证明,ATRA 和唑来膦酸的联合使用在转录或翻译水平上均能强烈诱导人雄激素和药物难治性前列腺癌细胞 DU-145 中的凋亡相关细胞死亡。当暴露于联合治疗时,促凋亡基因(如肿瘤坏死因子受体超家族(TNFRSF)、Bad、Bax、Fas、FADD)的表达被诱导,而凋亡抑制基因或蛋白(如凋亡抑制因子家族(IAPs)的成员、MCL-1、LTBR、p53 和 bcl-2)的表达则减少。由于这种新的联合治疗方案比传统细胞毒性药物的副作用少,因此对于老年前列腺癌患者的治疗可能是一个不错的选择。