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Tumor mechanics and metabolic dysfunction
- Source :
- Free radical biologymedicine. 79
- Publication Year :
- 2014
-
Abstract
- Desmosplasia is a characteristic of most solid tumors and leads to fibrosis through abnormal extracellular matrix (ECM) deposition, remodeling and post translational modifications. The resulting stiff tumor stroma not only compromises vascular integrity to induce hypoxia and impede drug delivery, but also promotes aggressiveness by potentiating the activity of key growth, invasion, and survival pathways. Intriguingly, many of the pro-tumorigenic signaling pathways which are mechanically activated by ECM stiffness also promote glucose uptake and aerobic glycolysis, and an altered metabolism is a recognized hallmark of cancer. Indeed, emerging evidence suggests that metabolic alterations and an abnormal ECM may cooperatively drive cancer cell aggression and treatment resistance. Accordingly, improved methods to monitor tissue mechanics and metabolism promise to improve diagnostics and treatments to ameliorate ECM stiffening and elevated mechanosignaling may improve patient outcome. Here we discuss the interplay between ECM mechanics and metabolism in tumor biology and suggest that monitoring these processes and targeting their regulatory pathways may improve diagnostics, therapy, and the prevention of malignant transformation.
- Subjects :
- Biochemistry & Molecular Biology
Free radicals
Biology
Medical Biochemistry and Metabolomics
Biochemistry
Article
Malignant transformation
Extracellular matrix
Medicinal and Biomolecular Chemistry
Mechanosignaling
Fibrosis
Physiology (medical)
Neoplasms
medicine
Tumor Microenvironment
2.1 Biological and endogenous factors
Humans
Aetiology
Tumor metabolism
Cancer
Tumor microenvironment
Prevention
Mechanics
Hypoxia (medical)
medicine.disease
Extracellular Matrix
Anaerobic glycolysis
Cancer cell
Disease Progression
Biochemistry and Cell Biology
medicine.symptom
Signal transduction
ECM stiffness
Subjects
Details
- ISSN :
- 18734596
- Volume :
- 79
- Database :
- OpenAIRE
- Journal :
- Free radical biologymedicine
- Accession number :
- edsair.doi.dedup.....3880f0ed93c0a50fdd7e8ba8c98626d9