Centro di Ricerche Oncologiche di Mercogliano (CROM), Mercogliano (AV), Italy.
Cell Death Dis. 2013 May 23;4(5):e641. doi: 10.1038/cddis.2013.165.
The nitrogen-containing bisphosphonates (N-BP) zoledronic acid (ZOL) inhibits osteoclast-mediated bone resorption, and it is used to prevent skeletal complications from bone metastases. ZOL has also demonstrated anticancer activities in preclinical models and, recently, in cancer patients, highlighting the interest in determining eventual mechanisms of resistance against this agent. In our study, we selected and characterised a resistant subline of prostate cancer (PCa) cells to better understand the mechanisms, by which tumour cells can escape the antitumour effect of ZOL. DU145R80-resistant cells were selected in about 5 months using stepwise increasing concentrations of ZOL from DU145 parental cells. DU145R80 cells showed a resistance index value of 5.5 and cross-resistance to another N-BP, pamidronate, but not to the non-nitrogen containing BP clodronate. Notably, compared with DU145 parental cells, DU145R80 developed resistance to apoptosis and anoikis, as well as overexpressed the anti-apoptotic protein Bcl-2 and oncoprotein c-Myc. Moreover, DU145R80 cells underwent epithelial to mesenchymal transition (EMT) and showed increased expression of the metalloproteases MMP-2/9, as well as increased invading capability. Interestingly, compared with DU145, DU145R80 cells also increased the gene expression and protein secretion of VEGF and the cytokines Eotaxin-1 and IL-12. At the molecular level, DU145R80 cells showed strong activation of the p38-MAPK-dependent survival pathway compared with parental sensitive cells. Moreover, using the p38-inhibitor SB203580, we completely reversed the resistance to ZOL, as well as EMT marker expression and invasion. Furthermore, SB203580 treatment reduced the expression of VEGF, Eotaxin-1, IL-12, MMP-9, Bcl-2 and c-Myc. Thus, for the first time, we demonstrate that the p38-MAPK pathway can be activated under continuous extensive exposure to ZOL in PCa cells and that the p38-MAPK pathway has a critical role in the induction of resistance, as well as in the acquisition of a more aggressive and invasive phenotype.
含氮双膦酸盐(N-BP)唑来膦酸(ZOL)抑制破骨细胞介导的骨吸收,用于预防骨转移引起的骨骼并发症。ZOL 在临床前模型和最近的癌症患者中也表现出抗癌活性,这凸显了确定该药物潜在耐药机制的重要性。在我们的研究中,我们选择并鉴定了前列腺癌细胞的耐药亚系,以更好地了解肿瘤细胞逃避 ZOL 抗肿瘤作用的机制。从 DU145 亲本细胞开始,通过逐步增加 ZOL 的浓度,大约 5 个月后选择出 DU145R80 耐药细胞。DU145R80 细胞的耐药指数值为 5.5,对另一种 N-BP 帕米膦酸具有交叉耐药性,但对不含氮的 BP 氯膦酸没有耐药性。值得注意的是,与 DU145 亲本细胞相比,DU145R80 细胞对细胞凋亡和失巢凋亡产生耐药性,并且过度表达抗凋亡蛋白 Bcl-2 和癌蛋白 c-Myc。此外,DU145R80 细胞发生上皮间质转化(EMT),并表现出金属蛋白酶 MMP-2/9 的表达增加以及侵袭能力增强。有趣的是,与 DU145 相比,DU145R80 细胞还增加了 VEGF、细胞因子 Eotaxin-1 和 IL-12 的基因表达和蛋白分泌。在分子水平上,与亲本敏感细胞相比,DU145R80 细胞中 p38-MAPK 依赖性存活途径的激活明显更强。此外,使用 p38 抑制剂 SB203580,我们完全逆转了对 ZOL 的耐药性,以及 EMT 标志物表达和侵袭。此外,SB203580 处理降低了 VEGF、Eotaxin-1、IL-12、MMP-9、Bcl-2 和 c-Myc 的表达。因此,我们首次证明 p38-MAPK 途径可以在 PCa 细胞中持续广泛暴露于 ZOL 下被激活,并且 p38-MAPK 途径在诱导耐药性以及获得更具侵袭性和侵袭性表型方面起着关键作用。