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Cellular senescence is characterized by a stable arrest in the cell cycle and encompasses a range of cellular changes that culminate in the development of a complex, pro-inflammatory secretory profile known as the senescence-associated secretory phenotype (SASP), which plays a critical role in fibrosis and tumors by affecting numerous processes, including invasion and therapy resistance 10

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2D), which had significant formation when EGT was oxidized with hypochlorite

Each of its four components targets a different bottleneck in the repair-and-remodel cascade: GHK-Cu drives extracellular-matrix remodeling and copper delivery, BPC-157 supports angiogenesis (new blood-vessel formation) and blood flow, TB-500 (a thymosin beta-4 fragment) promotes cell migration and actin regulation, and KPV is an anti-inflammatory tripeptide