3D tumor spheroids: morphological alterations a yardstick to anti-cancer drug response

Anna Senrung, Sakshi Lalwani, Divya Janjua, Tanya Tripathi, Jasleen Kaur, Netra Ghuratia, Nikita Aggarwal, Arun Chhokar, Joni Yadav, Apoorva Chaudhary, Udit Joshi, Alok Chandra Bharti
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Abstract

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.
三维肿瘤球体:形态改变是抗癌药物反应的标尺
肿瘤球体是一种具有良好特征的三维培养系统之一,具有与缺氧核心的无血管实体瘤阶段的生理组织结构和复杂性非常相似的特点。它们在医药科学和抗癌药物研究领域有着广泛的应用。然而,在确定产生具有均匀大小和形状的球体的最佳技术,评估实验结果或大规模生产方面的困难往往限制了它们在抗癌研究和高通量药物筛选中的使用。近年来,一些研究已经展示了各种简单的技术来生成均匀尺寸的三维球体,包括悬挂滴(HD)、液体覆盖技术(LOT)和微流体方法。除了生化分析外,形态学改变和染色技术适合用于评估3D球体模型内的实验结果。在有效的抗癌药物治疗下,三维肿瘤球体的形态改变,如球体尺寸减小,球体致密性和完整性或光滑表面的丧失,是高度可靠的。这些改变可以显著减少对生化分析和染色技术的需求,从而节省时间和成本。这篇文章具体地涵盖了各种可用的程序在球体生成。为了实用性,我们补充了我们的综述研究,使用HD和LOT方法生成胶质母细胞瘤U87球体。此外,我们还纳入了用阿霉素治疗U87球体对球体形态的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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