阿霉素和钙化二醇联合作用对MCF-7乳腺癌细胞的影响

Oliwia Abramczyk, Sylwia Stawieraj, Agnieszka Mlicka, Wioletta Zielińska, Paweł Niewiadomski, Marta Hałas-Wiśniewska, M. Izdebska
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引用次数: 0

摘要

乳腺癌是女性最常见的癌症之一。目前对乳腺癌患者联合治疗的建议仍在制定中,人们正在寻求更成功的新疗法。一种相对较新的方法是将细胞抑制剂与维生素联合使用。因此,本研究旨在阐明钙化二醇[25(OH)D3]与阿霉素联用是否会影响MCF-7乳腺癌细胞系对细胞抑制剂的反应。材料和方法:在MCF-7细胞系中,作者使用MTT法评估细胞毒性,使用流式细胞术分析细胞周期和细胞死亡机制,并检查细胞骨架结构和细胞形态。结果:阿霉素与钙化二醇按1:1的比例联用具有协同作用,使细胞存活率呈剂量依赖性降低。进一步的研究表明,这是由于这些化合物组合的促凋亡和坏死作用。细胞骨架的组织和细胞形态也发生了变化。此外,在MCF-7细胞中发现了内吞的特征。结论:阿霉素与钙化二醇的协同作用可显著降低MCF-7乳腺癌细胞的生存能力。考虑到阿霉素的心脏毒性,通过降低细胞抑制剂剂量来诱导预期的效果具有重要的临床意义。另一个非常有趣的方面是本研究中诱导的内吞过程,它可能具有双重性质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of combined action of doxorubicin and calcifediol on MCF-7 breast cancer cells
Introduction : Breast cancer is one of the most common cancers in women. Current recommendations for combination therapy in patients with breast cancer are still being developed and new therapies with greater success are sought. A relatively new approach is the administration of cytostatics in combination with vitamins. Hence, the study aimed to clarify whether the combination of calcifediol [25(OH)D3] with doxorubicin affects the response of the MCF-7 breast cancer cell line to the cytostatic. Material and methods : In the MCF-7 cell line, the authors assessed cytotoxicity using the MTT assay, analysed the cell cycle and cell death mechanism using flow cytometry, and examined the structure of the cytoskeleton and cell morphology. Results : The results showed that doxorubicin in combination with calcifediol in a 1:1 ratio showed a synergistic effect resulting in a dose-dependent decrease in cell survival. Further studies have shown that this is due to the pro-apoptotic and necrotic effects of the combination of these compounds. There were also changes in the organization of the cytoskeleton and cell morphology. In addition, features of entosis were noted in MCF-7 cells. Conclusion : The synergistic effect of doxorubicin and calcifediol significantly reduced the viability of MCF-7 breast cancer cells. Inducing the desired effect by lowering the cytostatic dose is of great clinical importance, taking into account the cardiotoxicity of doxorubicin. Another very interesting aspect is the entosis process induced in the present research, which may have a dual nature.
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