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INSIDIA 2.0 高通量分析 3D 癌症模型:用于脑胶质瘤和胰腺癌的石墨烯量子点光热治疗的多参数定量分析。

INSIDIA 2.0 High-Throughput Analysis of 3D Cancer Models: Multiparametric Quantification of Graphene Quantum Dots Photothermal Therapy for Glioblastoma and Pancreatic Cancer.

机构信息

Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Largo Francesco Vito 1, 00168 Rome, Italy.

Fondazione Policlinico Universitario A. Gemelli IRCSS, 00168 Rome, Italy.

出版信息

Int J Mol Sci. 2022 Mar 16;23(6):3217. doi: 10.3390/ijms23063217.

Abstract

Cancer spheroids are in vitro 3D models that became crucial in nanomaterials science thanks to the possibility of performing high throughput screening of nanoparticles and combined nanoparticle-drug therapies on in vitro models. However, most of the current spheroid analysis methods involve manual steps. This is a time-consuming process and is extremely liable to the variability of individual operators. For this reason, rapid, user-friendly, ready-to-use, high-throughput image analysis software is necessary. In this work, we report the INSIDIA 2.0 macro, which offers researchers high-throughput and high content quantitative analysis of in vitro 3D cancer cell spheroids and allows advanced parametrization of the expanding and invading cancer cellular mass. INSIDIA has been implemented to provide in-depth morphologic analysis and has been used for the analysis of the effect of graphene quantum dots photothermal therapy on glioblastoma (U87) and pancreatic cancer (PANC-1) spheroids. Thanks to INSIDIA 2.0 analysis, two types of effects have been observed: In U87 spheroids, death is accompanied by a decrease in area of the entire spheroid, with a decrease in entropy due to the generation of a high uniform density spheroid core. On the other hand, PANC-1 spheroids' death caused by nanoparticle photothermal disruption is accompanied with an overall increase in area and entropy due to the progressive loss of integrity and increase in variability of spheroid texture. We have summarized these effects in a quantitative parameter of spheroid disruption demonstrating that INSIDIA 2.0 multiparametric analysis can be used to quantify cell death in a non-invasive, fast, and high-throughput fashion.

摘要

肿瘤球体是一种体外 3D 模型,由于能够在体外模型上对纳米粒子进行高通量筛选和联合纳米粒子-药物治疗,因此在纳米材料科学中变得至关重要。然而,目前大多数球体分析方法都涉及手动步骤。这是一个耗时的过程,并且非常容易受到个体操作人员的变化影响。出于这个原因,需要快速、用户友好、即用型、高通量的图像分析软件。在这项工作中,我们报告了 INSIDIA 2.0 宏,它为研究人员提供了高通量和高内涵定量分析体外 3D 癌细胞球体的方法,并允许对扩展和入侵的癌细胞团进行高级参数化。INSIDIA 已经被实现用于进行深入的形态分析,并已被用于分析石墨烯量子点光热疗法对神经胶质瘤(U87)和胰腺癌(PANC-1)球体的影响。通过 INSIDIA 2.0 分析,观察到了两种类型的效果:在 U87 球体中,死亡伴随着整个球体面积的减少,由于产生了高均匀密度的球体核心,熵值降低。另一方面,由于纳米颗粒光热破坏导致的 PANC-1 球体死亡伴随着整体面积和熵值的增加,这是由于球体完整性的逐渐丧失和球体纹理的可变性增加所致。我们已经在球体破坏的定量参数中总结了这些效果,表明 INSIDIA 2.0 多参数分析可用于以非侵入性、快速和高通量的方式定量细胞死亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5028/8948775/601b33171cad/ijms-23-03217-g001.jpg

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