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Docetaxel/zoledronic acid combination triggers apoptosis synergistically through downregulating antiapoptotic Bcl-2 protein level in hormone-refractory prostate cancer cells

机译:多西紫杉醇/唑来膦酸联合通过下调激素难治性前列腺癌细胞中抗凋亡的Bcl-2蛋白水平来协同触发凋亡

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摘要

Docetaxel, a semi-synthetic taxane analogue, is used effectively in the treatment of metastatic prostate cancer. Zoledronic acid, the most potent member of bisphosphonates, has shown pleiotropic anti-tumoral effects on prostate cancer cells. We have explored the possible additive/synergistic effects and the apoptotic pathways induced by combination treatment of docetaxel and zoledronic acid in hormone and drug refractory, PC-3 and DU-145 prostate cancer cells. Combination of docetaxel and zoledronic acid synergistically inhibits cell growth in PC-3 and DU-145 cells. Moreover, this effect was due to downregulation of antiapoptotic protein Bcl-2 in PC-3 and DU-145 cells. In conclusion, docetaxel/zoledronic acid combination is potentially a novel and effective approach for the treatment of prostate cancer.
机译:多西他赛是一种半合成紫杉烷类似物,可有效用于治疗转移性前列腺癌。唑来膦酸是最有效的双膦酸酯成员,对前列腺癌细胞具有多效抗肿瘤作用。我们已经探索了多西他赛和唑来膦酸联合治疗荷尔蒙和药物难治性,PC-3和DU-145前列腺癌细胞中可能产生的加性/协同效应和凋亡途径。多西紫杉醇和唑来膦酸的组合协同抑制PC-3和DU-145细胞的细胞生长。此外,该作用归因于PC-3和DU-145细胞中抗凋亡蛋白Bcl-2的下调。总之,多西他赛/唑来膦酸的组合可能是治疗前列腺癌的一种新颖有效的方法。

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