Tenta R, Pitulis N, Tiblalexi D, Consoulas C, Katopodis H, Konstantinidou E, Manoussakis M, Kletsas D, Alexis M N, Poyatzi A, Koutsilieris M
Department of Experimental Physiology, Medical School, University of Athens, Goudi-Athens Greece.
Horm Metab Res. 2008 Nov;40(11):737-45. doi: 10.1055/s-2008-1078753. Epub 2008 Jun 18.
The aim of our study was to analyze the action of zoledronic acid on MG-63 human osteosarcoma cells. The proliferation of MG-63 cells was inhibited by either continuous or pulsatile exposures of zoledronic acid in a dose-dependent manner (10-250 microM). Zoledronic acid did not produce evidence of MG-63 cell death when administered at 100 mM for 48 hours, but only after exposure of 96 hours. Zoledronic acid (100 microM) increased the distribution of MG-63 cells in G0/G1 phase, however, it did not increase the adriamycin-induced apoptosis. In addition, zoledronic acid action was partially neutralized by exogenous administration of geranylgeranyl pyrophosphate (GGPP), but not by farnesyl pyrophosphate (FPP). Furthermore, zoledronic acid resulted in the attenuation of the prenylated form of Ras. Zoledronic acid and EDTA increased fluorescence of Fluo-3 loaded MG-63 cells in a similar pattern. This increase was owing to the release of Ca2+ from intracellular stores since zoledronic acid failed to reveal such a change to intracellular Ca2+ when cells were previously treated with 1 mM caffeine. Moreover, zoledronic acid significantly decreased the expression of estrogen receptor alpha (ERalpha) whereas it did not change significantly the expression of estrogen receptor beta (ERbeta) in MG-63 cells. These data suggest that zoledronic acid can control the proliferation and the differentiation of osteosarcoma-like cells.
我们研究的目的是分析唑来膦酸对MG-63人骨肉瘤细胞的作用。唑来膦酸连续或脉冲暴露均以剂量依赖性方式(10 - 250微摩尔)抑制MG-63细胞的增殖。当以100毫摩尔给药48小时时,唑来膦酸未产生MG-63细胞死亡的证据,但仅在暴露96小时后才出现。唑来膦酸(100微摩尔)增加了MG-63细胞在G0/G1期的分布,然而,它并未增加阿霉素诱导的细胞凋亡。此外,唑来膦酸的作用可被外源性给予香叶基香叶基焦磷酸(GGPP)部分中和,但不能被法尼基焦磷酸(FPP)中和。此外,唑来膦酸导致Ras的异戊二烯化形式减少。唑来膦酸和EDTA以类似模式增加了负载Fluo-3的MG-63细胞的荧光。这种增加是由于细胞内钙库释放Ca2+,因为当细胞预先用1毫摩尔咖啡因处理时,唑来膦酸未能显示出对细胞内Ca2+的这种变化。此外,唑来膦酸显著降低了雌激素受体α(ERα)的表达,而在MG-63细胞中它并未显著改变雌激素受体β(ERβ)的表达。这些数据表明唑来膦酸可以控制骨肉瘤样细胞的增殖和分化。