Institute of Biochemistry, Faculty of Biology, University of Warsaw, Miecznikowa 1, 02-096 Warsaw, Poland.
Oncol Rep. 2012 Jan;27(1):281-5. doi: 10.3892/or.2011.1500. Epub 2011 Oct 12.
Inhibitors of CK2 kinase inhibit cell proliferation and induce apoptosis in numerous cancer cell lines. Due to these properties, they are considered potentially useful in anticancer therapy. In this study, we show that the exact effect of the specific CK2 inhibitor TBB on PC-3 human prostate cancer cell viability depends on the time schedule of administration: it was not observed when the treatment was directly followed by the viability assay but it appeared when the treatment and the assay were separated by a 24-h incubation without the inhibitor. Such a pattern was maintained when the TBB treatment was combined with either camptothecin or TRAIL. The time schedule-dependence of cell viability was not reflected by a similar dependence of induction of apoptosis. Despite this, the schedule in which a treatment with the CK2 inhibitor precedes that with an anticancer drug seems to be a good choice for a potential therapy against androgen-refractory prostate cancer.
CK2 激酶抑制剂可抑制多种癌细胞系的增殖并诱导其凋亡。由于这些特性,它们被认为在癌症治疗中有潜在的应用价值。在这项研究中,我们发现特定的 CK2 抑制剂 TBB 对 PC-3 人前列腺癌细胞活力的确切影响取决于给药的时间安排:当处理直接跟随活力测定时,没有观察到这种影响,但当处理和测定通过 24 小时无抑制剂孵育分开时,这种影响就出现了。当 TBB 处理与喜树碱或 TRAIL 联合使用时,这种模式得以维持。细胞活力的时间安排依赖性并没有反映在凋亡诱导的类似依赖性上。尽管如此,在 CK2 抑制剂治疗之前进行抗癌药物治疗的时间安排似乎是治疗雄激素难治性前列腺癌的一个不错选择。