Alqahtani Saud, Alqahtani Taha, Venkatesan Krishnaraju, Sivadasan Durgaramani, Ahmed Rehab, Sirag Nizar, Elfadil Hassabelrasoul, Abdullah Mohamed Hanem, T A Haseena, Elsayed Ahmed Rasha, Muralidharan Pooja, Paulsamy Premalatha
Department of Pharmacology, College of Pharmacy, King Khalid University, Abha 62521, Saudi Arabia.
Department of Pharmaceutics, College of Pharmacy, Jazan University, Jazan 45142, Saudi Arabia.
Cells. 2025 Apr 17;14(8):608. doi: 10.3390/cells14080608.
Cellular senescence regulates aging, tissue maintenance, and disease progression through the Senescence-Associated Secretory Phenotype (SASP), a secretory profile of cytokines, chemokines, growth factors, and matrix-remodeling enzymes. While transient SASP aids wound healing, its chronic activation drives inflammation, fibrosis, and tumorigenesis. This review examines SASP's molecular regulation, dual roles in health and pathology, and therapeutic potential. The following two main strategies are explored: senescence clearance, which eliminates SASP-producing cells, and SASP modulation, which refines secretion to suppress inflammation while maintaining regenerative effects. Key pathways, including NF-κB, C/EBPβ, and cGAS-STING, are discussed alongside pharmacological, immunotherapeutic, gene-editing, and epigenetic interventions. SASP heterogeneity necessitates tissue-specific biomarkers for personalized therapies. Challenges include immune interactions, long-term safety, and ethical considerations. SASP modulation emerges as a promising strategy for aging, oncology, and tissue repair, with future advancements relying on multi-omics and AI-driven insights to optimize clinical outcomes.
细胞衰老通过衰老相关分泌表型(SASP)调节衰老、组织维持和疾病进展,SASP是细胞因子、趋化因子、生长因子和基质重塑酶的一种分泌谱。虽然短暂的SASP有助于伤口愈合,但其长期激活会引发炎症、纤维化和肿瘤发生。本综述探讨了SASP的分子调控、在健康和病理中的双重作用以及治疗潜力。探讨了以下两种主要策略:衰老清除,即消除产生SASP的细胞;SASP调节,即优化分泌以抑制炎症,同时保持再生效应。讨论了关键途径,包括NF-κB、C/EBPβ和cGAS-STING,以及药理学、免疫治疗、基因编辑和表观遗传干预措施。SASP的异质性需要组织特异性生物标志物来实现个性化治疗。挑战包括免疫相互作用、长期安全性和伦理考量。SASP调节成为衰老、肿瘤学和组织修复的一种有前景的策略,未来的进展依赖于多组学和人工智能驱动的见解来优化临床结果。