Devadass Jessy Mercy, Koyeli Girigoswami, Agnishwar Girigoswami
Wound healing is the critical process regulated through a harmonious coordination of cellular, molecular, pathological, and systemic communications. Normally, healing occurs in four overlapping phases, which are modified and controlled by various growth factor interactions and signaling pathways. Disruption of the tightly coordinated wound-healing cascade, together with aberrant protein signaling, mitochondrial dysfunction, antimicrobial resistance, sustained fibroblast activation, and maladaptive epigenetic reprogramming, drives pathological tissue repair culminating in chronic non-healing wounds, including diabetic, ischemic, and venous ulcers, as well as fibrotic outcomes such as hypertrophic and keloid scarring. The persistent fibroblast activation, reduced apoptosis, prolonged TGF-β activity, and severe fibrosis induced by mechanical methods trigger excessive healing, while existing therapies fail to manage these functions. Therefore, in order to develop advancements toward precise and personalized medicine, it is important to understand the various mechanisms involved in wound healing. The current review provides a comprehensive understanding of various fundamental mechanisms involved in wound healing, such as cellular, molecular, signaling pathways, genetic, epigenetic, pathological, immunological, and systemic mechanisms. Knowledge of these mechanisms and how they work under physiological as well as pathological conditions connects to clinical inefficiency, which helps to provide accurate medicine. A deeper mechanistic knowledge paves the way for developing innovative biomaterials; nanotechnology-based therapeutic strategies, specific drug delivery, molecular biomarkers, and scar-free healing of wounds, which enrich the future with advanced therapeutics and personalized medicine for wounds.