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用于纳米颗粒体外治疗筛选的 3D 肿瘤球体模型。

3D Tumor Spheroid Models for In Vitro Therapeutic Screening of Nanoparticles.

机构信息

Life Sciences Center, Vilnius University, Vilnius, Lithuania.

Laboratory of Drug Targets Histopathology, Institute of Cardiology, Lithuanian University of Health Sciences, Kaunas, Lithuania.

出版信息

Adv Exp Med Biol. 2021;1295:243-270. doi: 10.1007/978-3-030-58174-9_11.

Abstract

The anticancer activity of compounds and nanoparticles is most often determined in the cell monolayer. However, three-dimensional (3D) systems, such as tumor spheroids, are more representing the natural tumor microenvironment. They have been shown to have higher invasiveness and resistance to cytotoxic agents and radiotherapy compared to cells growing in 2D monolayer. Furthermore, to improve the prediction of clinical efficacy of drugs, in the past decades, even more sophisticated systems, such as multicellular 3D cultures, closely representing natural tumor microenvironment have been developed. Those cultures are formed from either cell lines or patient-derived tumor cells. Such models are very attractive and could improve the selection of tested materials for clinical trials avoiding unnecessary expensive tests in vivo. The microenvironment in tumor spheroids is different, and those differences or the interaction between several cell populations may contribute to different tumor response to the treatment. Also, different types of nanoparticles may have different behavior in 3D models, depending on their nature, physicochemical properties, the presence of targeting ligands on the surface, etc. Therefore, it is very important to understand in which cases which type of tumor spheroid is more suitable for testing specific types of nanoparticles, which conditions should be used, and which analytical method should be applied.

摘要

化合物和纳米粒子的抗癌活性通常在单层细胞中进行测定。然而,三维(3D)系统,如肿瘤球体,更能代表自然肿瘤微环境。与在 2D 单层中生长的细胞相比,它们显示出更高的侵袭性和对细胞毒性药物和放射治疗的抵抗力。此外,为了提高对药物临床疗效的预测,在过去几十年中,甚至更复杂的系统,如更紧密地代表自然肿瘤微环境的多细胞 3D 培养物,也已经被开发出来。这些培养物由细胞系或患者来源的肿瘤细胞组成。这些模型非常有吸引力,可以改进临床试验中测试材料的选择,避免不必要的昂贵的体内测试。肿瘤球体中的微环境不同,这些差异或几种细胞群体之间的相互作用可能导致肿瘤对治疗的反应不同。此外,不同类型的纳米粒子在 3D 模型中的行为可能不同,具体取决于它们的性质、物理化学特性、表面上存在的靶向配体等。因此,了解在哪些情况下哪种类型的肿瘤球体更适合测试特定类型的纳米粒子,应使用哪些条件以及应应用哪种分析方法是非常重要的。

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