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Inhibition of breast cancer cell proliferation in repeated and non-repeated treatment with zoledronic acid

机译:唑来膦酸重复和非重复治疗对乳腺癌细胞增殖的抑制作用

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Zoledronic acid is used to treat bone metastases and has been shown to reduce skeletal-related events and exert antitumor activity. The present in vitro study investigates the mechanism of action of Zoledronic Acid on breast cancer cell lines with different hormonal and HER2 patterns. Furthermore, we investigated the efficacy of repeated versus non-repeated treatments. The study was performed on 4 breast cancer cell lines (BRC-230, SkBr3, MCF-7 and MDA-MB-231). Non-repeated treatment (single exposure of 168 hrs’ duration) with zoledronic acid was compared with repeated treatment (separate exposures, each of 48 hrs’ duration, for a total of 168 hrs) at different dosages. A dose–response profile was generated using sulforhodamine B assay. Apoptosis was evaluated by TUNEL assay and biomolecular characteristics were analyzed by western blot. Zoledronic acid produced a dose-dependent inhibition of proliferation in all cell lines. Anti-proliferative activity was enhanced with the repeated treatment, proving to be statistically significant in the triple-negative lines. In these lines repeated treatment showed a cytocidal effect, with apoptotic cell death caused by caspase 3, 8 and 9 activation and decreased RAS and pMAPK expression. Apoptosis was not observed in estrogen receptor-positive line: p21 overexpression suggested a slowing down of cell cycle. A decrease in RAS and pMAPK expression was seen in HER2-overexpressing line after treatment. The study suggests that zoledronic acid has an antitumor activity in breast cancer cell lines. Its mechanism of action involves the decrease of RAS and RHO, as in osteoclasts. Repeated treatment enhances antitumor activity compared to non-repeated treatment. Repeated treatment has a killing effect on triple-negative lines due to apoptosis activation. Further research is warranted especially in the treatment of triple-negative breast cancer.
机译:唑来膦酸用于治疗骨转移,并已显示可减少骨骼相关事件并发挥抗肿瘤活性。目前的体外研究研究了唑来膦酸对具有不同激素和HER2模式的乳腺癌细胞系的作用机理。此外,我们研究了重复治疗与非重复治疗的疗效。该研究在4种乳腺癌细胞系(BRC-230,SkBr3,MCF-7和MDA-MB-231)上进行。将唑来膦酸的非重复治疗(单次暴露时间为168 hrs)与不同剂量的重复治疗(每次暴露48个小时,总共168 hrs)进行比较。使用磺基罗丹明B测定法产生剂量-反应曲线。通过TUNEL分析评估细胞凋亡,并通过蛋白质印迹分析生物分子特征。唑来膦酸在所有细胞系中均产生剂量依赖性的增殖抑制。重复治疗可增强抗增殖活性,在三阴性细胞系中证明具有统计学意义。在这些细胞系中,重复治疗显示出杀细胞作用,由caspase 3、8和9激活引起的凋亡性细胞死亡以及RAS和pMAPK表达降低。在雌激素受体阳性细胞系中未观察到细胞凋亡:p21过表达提示细胞周期减慢。治疗后在HER2过表达株中观察到RAS和pMAPK表达降低。该研究表明唑来膦酸在乳腺癌细胞系中具有抗肿瘤活性。如破骨细胞一样,其作用机制涉及RAS和RHO的降低。与非重复治疗相比,重复治疗可增强抗肿瘤活性。由于凋亡激活,重复治疗对三阴性细胞系具有杀伤作用。特别是在三阴性乳腺癌的治疗中,有待进一步研究。

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