Senrung Anna, Lalwani Sakshi, Janjua Divya, Tripathi Tanya, Kaur Jasleen, Ghuratia Netra, Aggarwal Nikita, Chhokar Arun, Yadav Joni, Chaudhary Apoorva, Joshi Udit, Bharti Alok Chandra
Molecular Oncology Laboratory, Department of Zoology, University of Delhi (North Campus), Delhi, 110007 India.
Neuropharmacology & Drug Delivery Laboratory, Zoology Department, Daulat Ram College, University of Delhi, Delhi, 110007 India.
In Vitro Model. 2023 Sep 20;2(6):219-248. doi: 10.1007/s44164-023-00059-8. eCollection 2023 Dec.
Tumor spheroids are one of the well-characterized 3D culture systems bearing close resemblance to the physiological tissue organization and complexity of avascular solid tumor stage with hypoxic core. They hold a wide-spread application in the field of pharmaceutical science and anti-cancer drug research. However, the difficulty in determining optimal technique for the generation of spheroids with uniform size and shape, evaluation of experimental outputs, or mass production often limits their usage in anti-cancer research and in high-throughput drug screening. In recent times, several studies have demonstrated various simple techniques for generating uniform-size 3D spheroids, including the hanging drop (HD), liquid overlay technique (LOT), and microfluidic approaches. Morphological alterations apart from biochemical assays, and staining techniques are suitably employed for the evaluation of experimental outcomes within 3D spheroid models. Morphological alterations in response to effective anti-cancer drug treatment in 3D tumor spheroids such as reduced spheroid size, loss of spheroid compactness and integrity or smooth surface, are highly reliable. These alterations can significantly reduce the need for biochemical assays and staining techniques, resulting in both time and cost savings. The present article specifically covers a variety of available procedures in spheroid generation. For practical applicability, we have supplemented our review study with the generation of glioblastoma U87 spheroids using HD and LOT methods. Additionally, we have also incorporated the outcome of U87 spheroid treatment with doxorubicin on spheroid morphology.
肿瘤球体是一种特征明确的三维培养系统,与具有缺氧核心的无血管实体瘤阶段的生理组织结构和复杂性极为相似。它们在制药科学和抗癌药物研究领域有着广泛的应用。然而,确定生成大小和形状均匀的球体的最佳技术、评估实验结果或进行大规模生产的难度,常常限制了它们在抗癌研究和高通量药物筛选中的应用。近年来,多项研究展示了多种生成大小均匀的三维球体的简单技术,包括悬滴法(HD)、液体覆盖技术(LOT)和微流控方法。除了生化检测外,形态学改变和染色技术也适用于评估三维球体模型中的实验结果。三维肿瘤球体在有效抗癌药物治疗下的形态学改变,如球体大小减小、球体紧实度和完整性丧失或表面变得光滑,是高度可靠的。这些改变可以显著减少生化检测和染色技术的需求,从而节省时间和成本。本文特别介绍了多种可用的球体生成方法。为了便于实际应用,我们在综述研究中补充了使用悬滴法和液体覆盖技术生成胶质母细胞瘤U87球体的内容。此外,我们还纳入了阿霉素处理U87球体对球体形态的影响结果。