Cisneros Castillo Liliana R, Oancea Andrei-Dumitru, Stüllein Christian, Régnier-Vigouroux Anne
Molecular Cell Biology, Institute of Zoology, Johannes Gutenberg University of Mainz, Mainz, Germany.
CLADIAC GmbH, Heidelberg, Germany.
Sci Rep. 2016 Jun 23;6:28375. doi: 10.1038/srep28375.
Multicellular tumor spheroids embedded in a matrix represent invaluable tools to analyze cell invasion. Spheroid sizes and invasiveness are the main observables easily measurable to evaluate effects of biological or pharmaceutical manipulations on invasion. They largely account for these 3-D platforms variability, leading to flaws in data interpretation. No method has been established yet that characterizes this variability and guarantees a reliable use of 3-D platforms. Spheroid initial/end sizes and invasiveness were systematically analyzed and compared in spheroids of U87MG cells generated by three different methods and embedded at different times in a collagen matrix. A normality test was used to characterize size distribution. We introduced the linearity-over-yield analysis as a novel mathematical tool to assess end sizes and invasion reproducibility. We further provide a proof of concept by applying these tools to the analysis of a treatment known to be effective beforehand. We demonstrate that implementation of these statistical and mathematical tools warranted a confident quantification and interpretation of in 3-D conducted assays. We propose these tools could be incorporated in a guideline for generation and use of 3-D platforms.
嵌入基质中的多细胞肿瘤球体是分析细胞侵袭的宝贵工具。球体大小和侵袭性是易于测量的主要可观测指标,用于评估生物或药物操作对侵袭的影响。它们在很大程度上导致了这些三维平台的变异性,从而导致数据解释存在缺陷。目前尚未建立表征这种变异性并保证三维平台可靠使用的方法。对通过三种不同方法生成并在不同时间嵌入胶原基质的U87MG细胞球体的初始/最终大小和侵袭性进行了系统分析和比较。使用正态性检验来表征大小分布。我们引入了产量线性分析作为一种新颖的数学工具,以评估最终大小和侵袭的可重复性。我们通过将这些工具应用于事先已知有效的治疗分析,进一步提供了概念验证。我们证明,这些统计和数学工具的实施保证了对三维实验进行可靠的量化和解释。我们建议这些工具可纳入三维平台生成和使用的指南中。