Dietary palmitic acid promotes a prometastatic memory via Schwann cells
Gloria Pascual # 1, Diana Domínguez # 2, Marc Elosúa-Bayes 3, Felipe Beckedorff 4, Carmelo Laudanna 2, Claudia Bigas 2, Delphine Douillet 5, Carolina Greco 6, Aikaterini Symeonidi 2, Inmaculada Hernández 2 3, Sara Ruiz Gil 3, Neus Prats 2, Coro Bescós 7, Ramin Shiekhattar 4, Moran Amit 8, Holger Heyn 3, Ali Shilatifard 9, Salvador Aznar Benitah 10 11
Affiliations expand
- PMID: 34759321
- DOI: 10.1038/s41586-021-04075-0
Abstract
Fatty acid uptake and altered metabolism constitute hallmarks of metastasis1,2, yet evidence of the underlying biology, as well as whether all dietary fatty acids are prometastatic, is lacking. Here we show that dietary palmitic acid (PA), but not oleic acid or linoleic acid, promotes metastasis in oral carcinomas and melanoma in mice. Tumours from mice that were fed a short-term palm-oil-rich diet (PA), or tumour cells that were briefly exposed to PA in vitro, remained highly metastatic even after being serially transplanted (without further exposure to high levels of PA). This PA-induced prometastatic memory requires the fatty acid transporter CD36 and is associated with the stable deposition of histone H3 lysine 4 trimethylation by the methyltransferase Set1A (as part of the COMPASS complex (Set1A/COMPASS)). Bulk, single-cell and positional RNA-sequencing analyses indicate that genes with this prometastatic memory predominantly relate to a neural signature that stimulates intratumoural Schwann cells and innervation, two parameters that are strongly correlated with metastasis but are aetiologically poorly understood3,4. Mechanistically, tumour-associated Schwann cells secrete a specialized proregenerative extracellular matrix, the ablation of which inhibits metastasis initiation. Both the PA-induced memory of this proneural signature and its long-term boost in metastasis require the transcription factor EGR2 and the glial-cell-stimulating peptide galanin. In summary, we provide evidence that a dietary metabolite induces stable transcriptional and chromatin changes that lead to a long-term stimulation of metastasis, and that this is related to a proregenerative state of tumour-activated Schwann cells.
© 2021. The Author(s), under exclusive licence to Springer Nature Limited.
Comment in
Alkan HF, Altea-Manzano P, Fendt SM.Cell Metab. 2022 Jan 4;34(1):7-9. doi: 10.1016/j.cmet.2021.12.015.PMID: 34986339
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