Mechanical Forces in Cutaneous Wound Healing: Emerging Therapies to Minimize Scar Formation

Excessive scarring is major clinical and financial burden in the United States. Improved therapies are necessary to reduce scarring, especially in patients affected by hypertrophic and keloid scars. Advances in our understanding of mechanical forces in the wound environment enable us to target mecha...

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Veröffentlicht in:Advances in wound care (New Rochelle, N.Y.) N.Y.), 2018-02, Vol.7 (2), p.47-56
Hauptverfasser: Barnes, Leandra A, Marshall, Clement D, Leavitt, Tripp, Hu, Michael S, Moore, Alessandra L, Gonzalez, Jennifer G, Longaker, Michael T, Gurtner, Geoffrey C
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Sprache:eng
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Zusammenfassung:Excessive scarring is major clinical and financial burden in the United States. Improved therapies are necessary to reduce scarring, especially in patients affected by hypertrophic and keloid scars. Advances in our understanding of mechanical forces in the wound environment enable us to target mechanical forces to minimize scar formation. Fetal wounds experience much lower resting stress when compared with adult wounds, and they heal without scars. Therapies that modulate mechanical forces in the wound environment are able to reduce scar size. Increased mechanical stresses in the wound environment induce hypertrophic scarring via activation of mechanotransduction pathways. Mechanical stimulation modulates integrin, Wingless-type, protein kinase B, and focal adhesion kinase, resulting in cell proliferation and, ultimately, fibrosis. Therefore, the development of therapies that reduce mechanical forces in the wound environment would decrease the risk of developing excessive scars. The development of novel mechanotherapies is necessary to minimize scar formation and advance adult wound healing toward the scarless ideal. Mechanotransduction pathways are potential targets to reduce excessive scar formation, and thus, continued studies on therapies that utilize mechanical offloading and mechanomodulation are needed.
ISSN:2162-1918
2162-1934
DOI:10.1089/wound.2016.0709