The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
Extracellular Matrix-Inspired Growth Factor Delivery Systems for Skin Wound Healing
Open accessAbstract
Significance: Growth factors are very promising molecules for the treatment of skin wounds. However, their translation to clinical use has been seriously limited, facing issues related to safety and cost-effectiveness. These problems may derive from the fact that growth factors are used at vastly supra-physiological levels without optimized delivery systems. Recent Advances: The extracellular matrix (ECM) plays a fundamental role in coordinating growth factor signaling. Therefore, understanding the mechanisms by which the ECM modulates growth factor activity is key for designing efficient growth factor-based therapies. Recently, several growth factor-binding domains have been discovered within various ECM proteins, and growth factor delivery systems integrating these ECM growth factor-binding domains showed promising results in animal models of skin wound healing. Moreover, a novel strategy consisting of engineering growth factors to target endogenous ECM could substantially enhance their efficacy, even when used at low doses. Critical Issues: Optimal delivery of growth factors often requires complex engineered biomaterial matrices, which can face regulatory issues for clinical translation. To simplify delivery systems and render strategies more applicable, growth factors can be engineered to optimally function with clinically approved biomaterials or with endogenous ECM present at the delivery site. Future Directions: Further development and clinical trials will reveal whether growth factor-based therapies can be used as main therapeutic approaches for skin wound healing. The future impact of these therapies will depend on our capacity to deliver growth factors more precisely, to improve efficacy, safety, and cost-effectiveness.
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Cites
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Self-citationRegulation of Wound Healing by Growth Factors and Cytokines
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The Extracellular Matrix: Not Just Pretty Fibrils
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Chronic Wound Pathogenesis and Current Treatment Strategies: A Unifying Hypothesis
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Self-citationGrowth factor binding to the pericellular matrix and its importance in tissue engineering☆
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The promotion of endothelial cell attachment and spreading using FNIII10 fused to VEGF-A165
Traub, S., Morgner, J., Martino, M. M., Höning, S., Swartz, M. A., Wickström, S. A., Hubbell, J. A., & Eming, S. A. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.04.050 · Cited by 42
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Cited by
Advanced Growth Factor Delivery Systems in Wound Management and Skin Regeneration
Park, J., Hwang, S., & Yoon, I.-S. (2017) · Molecules · doi:10.3390/molecules22081259 · Cited by 414
Xiao, J., Zhu, Y., Huddleston, S., Li, P., Xiao, B., Farha, O. K., & Ameer, G. A. (2018) · ACS Nano · doi:10.1021/acsnano.7b01850 · Cited by 396
Focus on the Contribution of Oxidative Stress in Skin Aging
Papaccio, F., D′Arino, A., Caputo, S., & Bellei, B. (2022) · Antioxidants · doi:10.3390/antiox11061121 · Cited by 396
Advances in Growth Factor Delivery for Bone Tissue Engineering
Oliveira, É. R., Nie, L., Podstawczyk, D., Allahbakhsh, A., Ratnayake, J., Brasil, D. L., & Shavandi, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22020903 · Cited by 258
Nanoparticle-based hyperthermia, a local treatment modulating the tumor extracellular matrix
Kolosnjaj-Tabi, J., Marangon, I., Nicolas-Boluda, A., Silva, A. K. A., & Gazeau, F. (2017) · Pharmacological Research · doi:10.1016/j.phrs.2017.07.010 · Cited by 86
Metadata
- Authors
- Briquez, P. S., Hubbell, J. A., & Martino, M. M.
- Venue
- Advances in Wound Care
- Publisher
- SAGE Publications
- Published
- 2015-08
- Volume
- 4
- Issue
- 8
- Pages
- 479-489
- ISSN
- 2162-1918 (ISSN-L)
- 2162-1934
- OpenAlex
- W2020984693
- Cited by
- 234
- References
- 7
- FWCI
- 21.42
- Type
- journal article
- Language
- en
- Open access
- green
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.