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An Optimized Workflow for the Analysis of Metabolic Fluxes in Cancer Spheroids Using Seahorse Technology. | LitMetric

AI Article Synopsis

  • Three-dimensional cancer models, like spheroids, replicate tumor biology better than traditional 2D cultures, making them valuable for studying cancer metabolism.
  • The Agilent Seahorse XFe96 system offers insights into cancer cell metabolism, but its use with 3D cultures hasn't been fully refined until now.
  • An optimized workflow improves spheroid uniformity and allows for detailed metabolic analysis, revealing that metabolic variations are primarily due to the cancer cell line rather than spheroid size.

Article Abstract

Three-dimensional cancer models, such as spheroids, are increasingly being used to study cancer metabolism because they can better recapitulate the molecular and physiological aspects of the tumor architecture than conventional monolayer cultures. Although Agilent Seahorse XFe96 (Agilent Technologies, Santa Clara, CA, United States) is a valuable technology for studying metabolic alterations occurring in cancer cells, its application to three-dimensional cultures is still poorly optimized. We present a reliable and reproducible workflow for the Seahorse metabolic analysis of three-dimensional cultures. An optimized protocol enables the formation of spheroids highly regular in shape and homogenous in size, reducing variability in metabolic parameters among the experimental replicates, both under basal and drug treatment conditions. High-resolution imaging allows the calculation of the number of viable cells in each spheroid, the normalization of metabolic parameters on a per-cell basis, and grouping of the spheroids as a function of their size. Multivariate statistical tests on metabolic parameters determined by the Mito Stress test on two breast cancer cell lines show that metabolic differences among the studied spheroids are mostly related to the cell line rather than to the size of the spheroid. The optimized workflow allows high-resolution metabolic characterization of three-dimensional cultures, their comparison with monolayer cultures, and may aid in the design and interpretation of (multi)drug protocols.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8909358PMC
http://dx.doi.org/10.3390/cells11050866DOI Listing

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