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脂质核纳米胶囊包封克服了肺癌细胞对维甲酸的耐药性。

Encapsulation in lipid-core nanocapsules overcomes lung cancer cell resistance to tretinoin.

机构信息

Programa de Pós-Graduação em Biotecnologia (PPGB), Grupo de Pesquisa em Oncologia Celular e Molecular, Biotecnologia/Centro de Desenvolvimento Tecnológico, Universidade Federal de Pelotas, Pelotas, Brazil.

Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.

出版信息

Eur J Pharm Biopharm. 2014 May;87(1):55-63. doi: 10.1016/j.ejpb.2014.02.003. Epub 2014 Feb 11.

DOI:10.1016/j.ejpb.2014.02.003
PMID:24525073
Abstract

Tretinoin is a retinoid derivative that has an antiproliferative effect on several kinds of tumours. Human lung adenocarcinoma epithelial cell lines (A549) exhibit a profound resistance to the effects of tretinoin. Nanocarriers seem to be a good alternative to overcomecellular resistance to drugs. The aim of this study was to test whether tretinoin-loaded lipid-core nanocapsules exert anantitumor effect on A549 cells. A549 cells were incubated with free tretinoin (TTN), blank nanocapsules (LNC) and tretinoin-loaded lipid-core nanocapsules (TTN-LNC). Data from evaluation of DNA content and Annexin V binding assay by flow cytometry showed that TTN-LNC induced apoptosis and cell cycle arrest at the G1-phase while TTN did not. TTN-LNC showed higher cytotoxic effects than TTN on A549 cells evaluated by MTT and LIVE/DEAD cell viability assay. Gene expression profiling identified up-regulated expression of gene p21 by TTN-LNC, supporting the cell cycle arrest effect. These results showed for the first time that TTN-LNC are able to overcome the resistance of adenocarcinoma cell line A549 to treatment with TTN by inducing apoptosis and cell cycle arrest, providing support for their use in applications in lung cancer therapy.

摘要

维 A 酸是一种维 A 衍生物,对多种肿瘤具有抗增殖作用。人肺腺癌细胞系(A549)对维 A 酸的作用表现出明显的耐药性。纳米载体似乎是克服细胞耐药性的一种很好的选择。本研究旨在测试载维 A 酸的脂核纳米囊是否对 A549 细胞具有抗肿瘤作用。用游离维 A 酸(TTN)、空白纳米囊(LNC)和载维 A 酸的脂核纳米囊(TTN-LNC)孵育 A549 细胞。通过流式细胞术评估 DNA 含量和 Annexin V 结合试验的数据表明,TTN-LNC 诱导细胞凋亡和细胞周期阻滞在 G1 期,而 TTN 则没有。MTT 和 LIVE/DEAD 细胞活力测定评估显示,与 TTN 相比,TTN-LNC 对 A549 细胞具有更高的细胞毒性作用。基因表达谱分析表明,TTN-LNC 上调了 p21 基因的表达,支持了细胞周期阻滞作用。这些结果首次表明,TTN-LNC 能够通过诱导细胞凋亡和细胞周期阻滞来克服腺癌细胞系 A549 对 TTN 治疗的耐药性,为其在肺癌治疗中的应用提供了支持。

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