唑来膦酸和醋酸Leuprolide影响Du-145向干细胞条件培养基的迁移

G. Montagna, F. Bertolini, B. Mognetti, G. Sibille
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引用次数: 0

摘要

前列腺癌(PCa)是最常见的泌尿生殖系统肿瘤,也是第三大特定的死亡原因,主要是因为骨转移。目前,PCa通常与GnRH类似物(醋酸leuprolide - la)和双膦酸盐(唑来膦酸- za)联合治疗。因此,本研究的目的是在体外研究这些药物对来自PCa (DU-145)的细胞系的影响。我们特别关注了药物可能在肿瘤进化和转移中发挥作用的一些关键方面,通过干扰活力、迁移和与骨细胞的相互作用。在5 μM浓度下,DU-145在接触48小时后出现ZA细胞毒性,而在更高浓度(100 μM)接触72小时后才出现LA细胞毒性。亚细胞毒性ZA和LA剂量均降低3D (transwell实验)PCa细胞迁移率。LA降低了pAkt/Akt比率,ZA也降低了pAkt/Akt比率,这与各自的抑制迁移比率一致,尽管ZA的影响不那么明显。细胞在间充质干细胞-间充质干细胞条件培养基(MSC- cm)中进行迁移试验,显著提高了迁移率(210%±2.2;P < 0.05)。ZA和LA的加入使条件介质的吸引效果消失。我们的研究结果表明,LA和ZA对癌细胞有直接的毒性作用。此外,即使在MSC施加的吸引刺激下,它们也能抑制细胞迁移,这可能有助于解释它们在限制转移中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Zoledronic Acid and Leuprolide Acetate Affect Du-145 Migration towards Stem Cell Conditioned Medium
Prostate cancer (PCa) is the most frequent genitourinary tumour and the third specific death cause, mostly because of bone metastasis. Currently, PCa is treated with GnRH analogues (leuprolide acetate-LA) and bisphosphonates (zoledronic acid-ZA) often in association. Thus, the aim of this work has been to study, in vitro, the effects of these drugs on cell line derived from PCa (DU-145). Particularly, we focused on some crucial aspects that drugs might play in tumor evolution and metastatization, by interfering with vitality, migration and interactions with bone cells. ZA cytotoxicity has been confirmed on DU-145 after 48-hours incubation at 5 μM, while LA cytotoxicity appears only after 72-hours contact at higher concentrations (100 μM). Both sub cytotoxic ZA and LA doses decreased 3D (transwell assay) PCa cell migration rate. pAkt/Akt ratio is diminished by LA and, even if less strikingly, by ZA, in agreement with the respective inhibition migration ratios. Cells underwent migration test in mesenchymal stem cells – MSC – conditioned medium (MSC-CM), which significantly increases the rate of migration (210%± 2.2; P<0.05). Addition of both ZA and LA quenched the attractive effect of conditioned medium. Our results suggest that LA and, mostly, ZA have a direct toxic effect on cancer cells. Furthermore, they inhibit cellular migration even under attractive stimuli exerted by MSC, and this might contribute to explain their effect in limiting metastatization.
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