Glutaminase as a metabolic target of choice to counter acquired resistance to Palbociclib by colorectal cancer cells

Tarrado-Castellarnau, M.; Foguet, C.; Tarrago-Celada, J.; Palobart, M.; Hernandez-Carro, C.; Perarnau, J.; Zodda, E.; Polat, I. H.; Marin, S.; Suarez-Bonnet, A.; Lozano, J. J.; Yuneva, M.; Thomson, T. M.; Cascante, M.

doi:10.1101/2024.01.04.574237

bioRxiv · 10.1101/2024.01.04.574237

Glutaminase as a metabolic target of choice to counter acquired resistance to Palbociclib by colorectal cancer cells

Tarrado-Castellarnau, M.·Foguet, C.·Tarrago-Celada, J.·Palobart, M.·Hernandez-Carro, C.·Perarnau, J.·Zodda, E.·Polat, I. H.·Marin, S.·Suarez-Bonnet, A.·Lozano, J. J.·Yuneva, M.·Thomson, T. M.·Cascante, M.

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Abstract

Several mechanisms of resistance of cancer cells to cyclin-dependent kinase inhibitors (CDKi) have been identified, including the upregulation of metabolic regulators such as glutaminase. However, whether such mechanisms and targets are optimal has not been determined. Here, we have systematically analyzed metabolic reprogramming in colorectal cancer cells exposed to Palbociclib, a CDKi selectively targeting CDK4/6, or Telaglenestat, a selective glutaminase inhibitor. Through multiple approaches, we show that Palbociclib and Telaglenestat elicit complementary metabolic responses and are thus uniquely suited to counter the metabolic reprogramming induced by the reciprocal drug. As such, while Palbociclib induced reduced tumor growth in vivo, and Telaglenestat did not show a significant effect, the drug combination displayed a strong synergistic effect on tumor growth. Likewise, initial responses to Palbociclib were followed by signs of adaptation and resistance, which were prevented by combining Palbociclib with Telaglenestat. In conclusion, combination with Telaglenestat optimally forestalls acquired resistance to Palbociclib in cancer cells.

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Tarrado-Castellarnau, M., Foguet, C., Tarrago-Celada, J., Palobart, M., Hernandez-Carro, C., Perarnau, J., Zodda, E., Polat, I. H., Marin, S., Suarez-Bonnet, A., Lozano, J. J., Yuneva, M., Thomson, T. M., Cascante, M.. 2024-01-05. Glutaminase as a metabolic target of choice to counter acquired resistance to Palbociclib by colorectal cancer cells. https://doi.org/10.1101/2024.01.04.574237

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