Skip to content
Review Open access

Modulating senescence for therapeutic delivery

Sep 2026 · Med-X · Vol 4 · 0 citations · 87 references

TL;DR

Recent progress in elucidating the relationship between senescence and disease progression is summarized and representative delivery strategies that demonstrate superior therapeutic potential are shown.

Abstract

Senescence has emerged as a promising therapeutic target in diverse age-related diseases and cancer, owing to its critical roles in tissue homeostasis, chronic inflammation, and tumor progression. Accumulating evidence indicates that senescent cells contribute to disease pathology through various pathophysiological mechanisms. Despite growing interest in exploiting senescence for therapeutic benefit, achieving precise and controllable senescence modulation remains challenging. Current strategies, including senolytics that selectively eliminate senescent cells and senomorphics that suppress senescence-associated secretory phenotype factors, often suffer from limited specificity, off-target toxicity, and inadequate control over treatment timing and dosage. To overcome these limitations, recent research has increasingly focused on interdisciplinary approaches that integrate advances in materials science, nanotechnology, and molecular biology, particularly through the development of advanced delivery systems designed to improve targeting efficiency and therapeutic outcomes. In this review, we summarize recent progress in elucidating the relationship between senescence and disease progression and show representative delivery strategies that demonstrate superior therapeutic potential. Senescence appears to be an encouraging therapeutic target in various diseases. The clinical translation of conventional senotherapeutics remains a major challenge. Advanced drug delivery systems for the targeted modulation of senescent cells exhibit significant promise. Senescence appears to be an encouraging therapeutic target in various diseases. The clinical translation of conventional senotherapeutics remains a major challenge. Advanced drug delivery systems for the targeted modulation of senescent cells exhibit significant promise.

Read PDF

Similar papers

Review Open access Aug 2026

Targeting Cellular Senescence for Cancer Therapy

The biological mechanisms regulating cellular senescence are summarized, its contrasting roles in cancer development are highlighted, emerging therapeutic approaches are discussed, and current challenges and future directions for translating senescence-based therapies into clinical oncology are outlined.

Awateef Fatima, Saba Yousuf · 0 citations
Sep 2026

Senescence-directed nanotherapy ameliorates fibrosis and overcomes immune exclusion in cancer

Fibrotic remodeling of tissues and tumors establishes immunosuppressive microenvironments that drive organ dysfunction and, in cancer, limit response to immunotherapy. Senescent-like cells are conserved drivers of fibrosis and therapeutic targets, yet their functional heterogeneity complicates therapeutic intervention....

Clemens Hinterleitner, Valentin J. A. Barthet, Hailey V. Goldberg et al. · 0 citations
Review Aug 2026

The senescence-immune axis as a target for combining immunotherapy and senotherapy.

This review focuses on the molecular and cellular mechanisms through which SnCs modulate immune composition and function, emphasizing immune checkpoint ligands, stress-associated surface molecules, and senescence-associated transcriptional programs governing senescence-associated secretory phenotype (SASP) expression.

Fernanda Saez-Calazans, L. Grun, Lucas Emanuel Stein et al. · 0 citations
Review Open access Aug 2026

The Role of Cellular Senescence in Chronic Lung Diseases: Emerging Mechanisms and Translational Perspectives: A Narrative Review

Cellular senescence is one of the major risk factors for the onset and progression of chronic pulmonary diseases. Cellular senescence can be induced by diverse stressors, including genotoxic damage, oncogenic signaling, and therapeutic interventions. These senescent cells communicate via the release of multiple inflamm...

Shravani Etrouth, Yin Zhu, Duo Zhang · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.