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Mechanometabolism: recent findings on the intersection of cell adhesion, cell migration, and metabolism
Open accessAbstract
Chemical and mechanical cues within the extracellular matrix (ECM) can initiate intracellular signaling that changes an array of fundamental cell functions. In recent work, studies of cell-ECM adhesion have deepened to include the influence of the physical ECM on cell metabolism. Since many biological processes involve metabolic programs, changes to cellular metabolism in response to cues in the ECM can have marked effects on cell health. In this review, we describe molecular mechanisms associated with cell-ECM adhesion that are key players in metabolism-induced changes to cell behaviors, including migration. We first review how changes to metabolite availability in the extracellular environment or manipulation of metabolic machinery in cells impact focal adhesions. We then connect this work to recent findings regarding the reverse relationship, namely, how the manipulation of focal adhesion proteins or integrins feeds back to alter cell metabolism. Finally, we consider the latest findings from studies that describe how the mechanical properties of the ECM, primarily stiffness and confinement, alter cellular metabolism. We identify key areas of future investigation that may elucidate the molecular drivers that permit cells to respond to mechanical and chemical ECM cues by reprogramming their metabolism to better inform future diagnostics and therapeutics for disease states.
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“These mechanical cues have been shown to modulate transcriptional programs related to cell adhesion, survival, and drug resistance, leading to gene expression profiles that diverge significantly from those observed in ECM-free conditions [213,217,218].”
From Modeling Tumor Microenvironment Complexity In Vitro: Spheroids as Physiologically Relevant Tumor Models and Strategies for Their Analysis (2025) · cites this paper as [218]
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Sorted by citations
Shah, S., & D’Souza, G. G. M. (2025) · Cells · doi:10.3390/cells14100732 · Cited by 83
“These mechanical cues have been shown to modulate transcriptional programs related to cell adhesion, survival, and drug resistance, leading to gene expression profiles that diverge significantly from those observed in ECM-free conditions [213,217,218].”
Metadata
- Authors
- Fabiano, E. D., Poole, J. M., & Reinhart-King, C. A.
- Affiliations
- Vanderbilt University (US)
- University of Alabama (US)
- Vanderbilt University
- Venue
- American Journal of Physiology-Cell Physiology
- Publisher
- American Physiological Society
- Published
- 2025-06-01
- Volume
- 328
- Issue
- 6
- Pages
- C1866-C1879
- ISSN
- 0363-6143 (ISSN-L)
- 1522-1563
- PMC
- PMC12643094
- OpenAlex
- W4409770237
- Cited by
- 17
- References
- 2
- Citations by year
- 2026: 13 · 2025: 4
- FWCI
- 2.03
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- American Journal of Physiology-Cell Physiology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- Funders
- HHS | NIH | National Institute of General Medical Sciences (GM131178)
- W. M. Keck Foundation
- NSF | EDU | Division of Graduate Education (1937963)
- HHS | NIH | NCI | Division of Cancer Prevention, National Cancer Institute (CA271715)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- cell-matrix adhesion, cell migration, focal adhesions, integrins, extracellular matrix stiffness, cellular metabolism, metabolic reprogramming, mechanotransduction
- MeSH terms
- Animals, Cell Adhesion, Cell Movement, Energy Metabolism, Extracellular Matrix, Humans, Signal Transduction, Integrins, Focal Adhesions, Mechanotransduction, Cellular
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