Related Experiment Video
Updated: Feb 18, 2026

Induction and Validation of Cellular Senescence in Primary Human Cells
Published on: June 20, 2018
Cellular senescence and liver disease: Mechanisms and therapeutic strategies
1Department of Pathogenic Biology and Immunology of Medical School, Southeast University, Nanjing, Jiangsu, 210009, China.
Abstract:
Cellular senescence is a fundamental cell fate caused by several cellular injuries which results in irreversible cell cycle arrest yet remaining metabolically active across all species. Cellular senescence not only can prevent tumor occurrence by inhibiting the proliferation of injured cells, but also can affect the surrounding cells through the senescence-associated secretory phenotype (SASP). Attractively, accumulating evidence shows that cellular senescence is closely related to various liver diseases. Therapeutic opportunities based on targeting senescent cells and the SASP are considered to be potential strategy for liver diseases. However, although research on cell senescence has attracted widespread attention, the overview on detailed mechanism and biological function of cell senescence in liver disease is still largely unknown. The present review summarizes the specific role of cell senescence in various liver diseases, and updates the molecular mechanisms underlying cell senescence. Moreover, the review also explores new strategies for prevention and treatment of liver disease through promoting senescence or counteracting excessive pathological senescence.
Insights
Cellular senescence, a state of irreversible cell cycle arrest, plays a key role in liver disease. Targeting senescent cells and their secretory phenotype offers potential therapeutic strategies for liver conditions.
Area of Science:
- Cellular biology
- Hepatology
- Molecular mechanisms
Background:
- Cellular senescence is a conserved cell fate characterized by irreversible cell cycle arrest and metabolic activity.
- Senescence can prevent tumors but also influence surrounding cells via the senescence-associated secretory phenotype (SASP).
- Emerging evidence links cellular senescence to various liver diseases, highlighting its complex role.
Purpose of the Study:
- To review the specific roles of cellular senescence in diverse liver diseases.
- To update the understanding of molecular mechanisms driving senescence in the liver.
- To explore novel therapeutic strategies targeting senescence for liver disease prevention and treatment.
Main Methods:
- Literature review and synthesis of existing research on cellular senescence and liver disease.
- Analysis of molecular pathways involved in senescence induction and SASP.
- Evaluation of therapeutic approaches targeting senescent cells in preclinical and clinical studies.
Main Results:
- Cellular senescence is implicated in the pathogenesis and progression of multiple liver diseases.
- The senescence-associated secretory phenotype (SASP) contributes to liver inflammation and fibrosis.
- Targeting senescent cells shows promise in ameliorating liver injury and disease.
Conclusions:
- Cellular senescence is a critical factor in liver disease, with both protective and detrimental effects.
- Understanding the molecular basis of senescence in the liver is crucial for developing effective therapies.
- Targeting senescent cells and SASP represents a promising therapeutic avenue for liver diseases.
Related Concept Videos
Replicative Cell Senescence
Liver Regeneration
Cells of Liver
The liver comprises four major types of cells— hepatocytes, stellate, Kupffer, and sinusoidal endothelial cells. The hepatocytes are...
Aging
Cellular Clock Theory
The cellular clock theory posits that the human lifespan is closely tied to the finite capacity of cells to divide, a phenomenon governed by telomeres, which are protective caps at the ends of...
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow
Tissue Renewal without Stem Cells
However, failure of such a system...
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test

