aging isnt a scam but immortality almost certainly is Biology Diagrams Bi et al. propose the Senoreverse anti-aging strategy, which aims to reverse the proliferative arrest of senescent cells. Exosomal miR-302b is identified as a Senoreverse candidate that targets the cell cycle inhibitors Cdkn1a and Ccng2, rejuvenating aging mice by improving physical and cognitive functions, extending lifespan, and exhibiting no safety concerns throughout a 24-month observation
This improvement is primarily attributed to the restoration of cell proliferation rather than a change in cell identity. miR-302b exerts its rejuvenating effects by targeting specific pathways involved in senescence, such as the downregulation of cell cycle inhibitors Cdkn1a and Ccng2, known contributors to the maintenance of the senescent Cellular senescence is an aging mechanism characterized by cell cycle arrest and a senescence-associated secretory phenotype (SASP). Preclinical studies demonstrate that senolytic drugs, which Tight regulation of cell division is critical throughout life for normal developmental processes, tissue regeneration, aging, and recovery from cellular damage. Abnormal development, aging-related disease, or carcinogenesis may result from aberrant cell cycle control. Drugs targeting different phases of the cell cycle may be leveraged for various therapeutic purposes, such as synthetic
302b rejuvenates aging mice by reversing the proliferative ... Biology Diagrams
This Review summarizes current research on cellular senescence including its molecular basis and examines how drugs may be targeted against senescent cells to treat age-related multimorbidities. Aging is a complex and multifaceted process involving a variety of interrelated molecular mechanisms and cellular systems. Phenotypically, the biological aging process is accompanied by a gradual loss of cellular function and the systemic deterioration of multiple tissues, resulting in susceptibility to aging-related diseases. Emerging evidence suggests that aging is closely associated with Cellular aging occurs through cell cycle arrest, which is the result of extended DDR cascade signaling networks via MDC1, 53BP1, H2AX, ATM, ARF, P53, P13-Akt, BRAF, Sirtuins, NAD + , and so forth. These persistent cell cycle arrests initiated by DDR and other associated stress-induced signals promote a permanent state of cell cycle arrest
Cell senescence is often associated with increased ROS level, enhanced ฮฒ-galactosidase activity and cell cycle arrest [[36], [37], [38]]. In this study, we assessed the anti-aging properties of Anti-VCAM1-GM1@Q micelles in vitro using these parameters (Fig. 3 A). D-gal has been used to induce cell senescence in vitro [39].