以聚合物胶束为载体的马卡巴油能减少三阴性乳腺癌细胞的迁移和增殖

Davi T. Aleixo, Ana C. M. Gualberto, Ana B. C. dos S. Valle, Luan C. da Silva, Kézia C. B. Ferreira, Ari S. de O. Lemos, Rodrigo L. Fabri, Guilherme D. Tavares, Maurílio de S. Cazarim, Jacy Gameiro and Frederico Pittella
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引用次数: 0

摘要

三阴性乳腺癌(TNBC)约占所有乳腺癌病例的 10-15%,通常影响年轻女性和 BRCA1 基因突变的女性。它更具侵袭性,确诊后最初几年内的复发风险较高。由于其侵袭性强、治疗方案有限以及耐药性等原因,迫切需要替代性策略。在这种情况下,Macauba(Acrocomia aculeata)是一种南美棕榈,其果实富含抗氧化剂,含有脂肪酸、类胡萝卜素和酚类化合物,可以清除活性氧(ROS),保护细胞。我们的研究重点是制作含有马古巴果肉油的聚合物胶束(PM-MO),并评估其在细胞毒性、抗增殖和抗迁移方面对三阴性乳腺癌细胞的影响。在配制 PM-MO 之前,我们对马卡巴油进行了化学特性鉴定和测试。此外,PM-MO 的流体力学直径为 105 nm,多分散指数(PdI)为 0.12,Zeta 电位为 -17.5 mV。48 小时和 72 小时后,PM-MO 对三阴性乳腺癌细胞的细胞毒性增强,而对非肿瘤细胞则无毒性。克隆生成试验显示,在 PM-MO 的最高浓度下,细胞集落的形成减少了 97% 至 81.9%。用 PM-MO 处理可减少乳腺癌细胞在体外的迁移,这表明它具有作为抗转移剂的潜力。我们的结论是,生产 PM-MO 的方法产生了大小适中、分布均匀的纳米颗粒。细胞存活率、增殖和迁移测试的结果突显了 PM-MO 在未来针对三阴性乳腺癌的体内试验中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Macauba oil carried by polymeric micelles reduces migration and proliferation of triple-negative breast cancer cells

Macauba oil carried by polymeric micelles reduces migration and proliferation of triple-negative breast cancer cells

Triple-negative breast cancer (TNBC) accounts for about 10–15% of all breast cancer cases, often affecting younger women and those with a BRCA1 mutation. It is more aggressive and has a higher recurrence risk within the first few years after diagnosis. Due to its aggressive nature, limited treatment options, and drug resistance, alternative strategies are urgently needed. In this context, Macauba (Acrocomia aculeata) is a South American palm with antioxidant-rich fruits containing fatty acids, carotenoids, and phenolic compounds, which can remove reactive oxygen species (ROS) and protect cells. Our study focused on creating Macauba pulp oil-loaded polymeric micelles (PM-MO) and assessing their impact on triple-negative breast cancer cells in terms of cytotoxicity, antiproliferation, and antimigration. Before formulating PM-MO, we conducted chemical characterization and testing of Macauba oil. Further, PM-MO presented hydrodynamic diameters of 105 nm, polydispersity index (PdI) of 0.12 and Zeta potential of −17.5 mV. PM-MO showed enhanced cytotoxicity against triple negative breast cancer cells after 48h and 72h, while no toxicity was observed on non-tumor cells. The clonogenicity assay showed a reduction in the formation of cell colonies ranging from 97% to 81.9% at the highest concentration of PM-MO. Treatment with PM-MO reduced breast cancer cell migration in vitro, indicating potential as an anti-metastatic agent. We conclude that the method used to produce PM-MO yielded well-sized nanoparticles with uniform distribution. Results from cell viability, proliferation, and migration tests highlight its potential for future in vivo trials against triple-negative breast cancer.

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