Blocking tumor-intrinsic MNK1 kinase restricts metabolic adaptation and diminishes liver metastasis

Dysregulation of the mitogen-activated protein kinase interacting kinases 1/2 (MNK1/2)-eukaryotic initiation factor 4E (eIF4E) signaling axis promotes breast cancer progression. MNK1 is known to influence cancer stem cells (CSCs); self-renewing populations that support metastasis, recurrence, and chemotherapeutic resistance, making them a clinically relevant target. The precise function of MNK1 in regulating CSCs, however, remains unexplored. Here, we generated MNK1 knockout cancer cell lines, resulting in diminished CSC properties in vitro and slowed tumor growth in vivo. Using a multiomics approach, we functionally demonstrated that loss of MNK1 restricts tumor cell metabolic adaptation by reducing glycolysis and increasing dependence on oxidative phosphorylation. Furthermore, MNK1-null breast and pancreatic tumor cells demonstrated suppressed metastasis to the liver, but not the lung. Analysis of The Cancer Genome Atlas (TCGA) data from breast cancer patients validated the positive correlation between MNK1 and glycolytic enzyme protein expression. This study defines metabolic perturbations as a previously unknown consequence of targeting MNK1/2, which may be therapeutically exploited.

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Publication Details

Journal
Science Advances
Published
2024-09-13
DOI
https://doi.org/10.1126/sciadv.adi7673
Citations
5
Primary Topic
Cancer, Hypoxia, and Metabolism
Type
article
Field-Weighted Citation Impact
1.43
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article

Blocking tumor-intrinsic MNK1 kinase restricts metabolic adaptation and diminishes liver metastasis

Christophe Gonçalves, Fan Huang, Natascha Gagnon, Carolina Lopez Naranjo et al.
5 citations
Science Advances
Cancer, Hypoxia, and Metabolism
1.43
article

Blocking tumor-intrinsic MNK1 kinase restricts metabolic adaptation and diminishes liver metastasis

Christophe Gonçalves, Fan Huang, Natascha Gagnon, Carolina Lopez Naranjo, Samuel E.J. Preston, Paige A. McCallum, Eleanor Dakin, René P. Zahedi, Raúl Ernesto Flores González, Vincent R. Richard, Russell G. Jones, Wilson H. Miller, Pnina Brodt, Christoph H. Borchers, Stéphanie Perrino, Michael S. Dahabieh, Theodore Papadopoulos, Sonia Victoria Del Rincon, Matthew Leibovitch
article en
5 citations

Abstract

Dysregulation of the mitogen-activated protein kinase interacting kinases 1/2 (MNK1/2)-eukaryotic initiation factor 4E (eIF4E) signaling axis promotes breast cancer progression. MNK1 is known to influence cancer stem cells (CSCs); self-renewing populations that support metastasis, recurrence, and chemotherapeutic resistance, making them a clinically relevant target. The precise function of MNK1 in regulating CSCs, however, remains unexplored. Here, we generated MNK1 knockout cancer cell lines, resulting in diminished CSC properties in vitro and slowed tumor growth in vivo. Using a multiomics approach, we functionally demonstrated that loss of MNK1 restricts tumor cell metabolic adaptation by reducing glycolysis and increasing dependence on oxidative phosphorylation. Furthermore, MNK1-null breast and pancreatic tumor cells demonstrated suppressed metastasis to the liver, but not the lung. Analysis of The Cancer Genome Atlas (TCGA) data from breast cancer patients validated the positive correlation between MNK1 and glycolytic enzyme protein expression. This study defines metabolic perturbations as a previously unknown consequence of targeting MNK1/2, which may be therapeutically exploited.

Science AdvancesVol. 10(37)
Van Andel Institute (US), McGill University Health Centre (CA), Jewish General Hospital (CA), CancerCare Manitoba (CA), University of Manitoba (CA), McGill University (CA)
Good health and well-being
Openalex Percentile: Top 18%
Cancer, Hypoxia, and Metabolism
1.43
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