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  2. Physiological Cell Culture Media Tune Mitochondrial Bioenergetics and Drug Sensitivity in Cancer Cell Models

Physiological Cell Culture Media Tune Mitochondrial Bioenergetics and Drug Sensitivity in Cancer Cell Models

  • Cancers (Basel). 2022 Aug 13;14(16):3917. doi: 10.3390/cancers14163917.
Omar Torres-Quesada 1 2 Carolina Doerrier 3 Sophie Strich 1 Erich Gnaiger 3 Eduard Stefan 1 2
Affiliations

Affiliations

  • 1 Tyrolean Cancer Research Institute (TKFI), Innrain 66, 6020 Innsbruck, Austria.
  • 2 Institute of Biochemistry and Center for Molecular Biosciences, University of Innsbruck, Innrain 80/82, 6020 Innsbruck, Austria.
  • 3 Oroboros Instruments, Schoepfstrasse 18, 6020 Innsbruck, Austria.
Abstract

Two-dimensional cell cultures are established models in research for studying and perturbing cell-type specific functions. However, many limitations apply to the cell growth in a monolayer using standard Cell Culture media. Although they have been used for decades, their formulations do not mimic the composition of the human cell environment. In this study, we analyzed the impact of a newly formulated human plasma-like media (HPLM) on cell proliferation, mitochondrial bioenergetics, and alterations of drug efficacies using three distinct Cancer cell lines. Using high-resolution respirometry, we observed that cells grown in HPLM displayed significantly altered mitochondrial bioenergetic profiles, particularly related to mitochondrial density and mild uncoupling of respiration. Furthermore, in contrast to standard media, the growth of cells in HPLM unveiled mitochondrial dysfunction upon exposure to the FDA-approved kinase inhibitor sunitinib. This seemingly context-dependent side effect of this drug highlights that the selection of the Cell Culture medium influences the assessment of Cancer drug sensitivities. Thus, we suggest to prioritize media with a more physiological composition for analyzing bioenergetic profiles and to take it into account for assigning drug efficacies in the Cell Culture model of choice.

Keywords

cancer cells; cell bioenergetics; cell culture media; cell proliferation; kinase inhibitor; mitochondrial function.

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