Evaluation of Consistency in Spheroid Invasion Assays

• Published in: Scientific reports Vol. 6; no. 1; p. 28375
• Main Authors: Cisneros Castillo, Liliana R., Oancea, Andrei-Dumitru, Stüllein, Christian, Régnier-Vigouroux, Anne
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 23.06.2016; Nature Publishing Group
• Subjects: 13; 13/106; 14; 14/63; 631/67; 631/80; Cancer; Cell Culture Techniques - instrumentation; Cell Line, Tumor; Cell Movement; Cell Proliferation; Cells; Collagen; Collagen - chemistry; Humanities and Social Sciences; Humans; Kinases; Methods; Models, Statistical; multidisciplinary; Neoplasm Invasiveness; Normal distribution; Reproducibility of Results; Science; Signal transduction; Spheroids; Spheroids, Cellular - cytology; Spheroids, Cellular - pathology; Standard deviation; Tumor Cells, Cultured - cytology; Tumor Cells, Cultured - pathology; Tumors; Germany
• ISSN: 2045-2322; 2045-2322
• 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.