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Updated: Feb 5, 2026

Techniques to Induce and Quantify Cellular Senescence
Published on: May 1, 2017
Biomarkers of Cellular Senescence and Skin Aging
Audrey S Wang1, Oliver Dreesen1,2
1Cell Ageing, Skin Research Institute of Singapore (SRIS), A∗STAR, Singapore, Singapore.
Abstract:
Cellular senescence is an irreversible growth arrest that occurs as a result of different damaging stimuli, including DNA damage, telomere shortening and dysfunction or oncogenic stress. Senescent cells exert a pleotropic effect on development, tissue aging and regeneration, inflammation, wound healing and tumor suppression. Strategies to remove senescent cells from aging tissues or preneoplastic lesions can delay tissue dysfunction and lead to increased healthspan. However, a significant hurdle in the aging field has been the identification of a universal biomarker that facilitates the unequivocal detection and quantification of senescent cell types in vitro and in vivo. Mammalian skin is the largest organ of the human body and consists of different cell types and compartments. Skin provides a physical barrier against harmful microbes, toxins, and protects us from ultraviolet radiation. Increasing evidence suggests that senescent cells accumulate in chronologically aged and photoaged skin; and may contribute to age-related skin changes and pathologies. Here, we highlight current biomarkers to detect senescent cells and review their utility in the context of skin aging. In particular, we discuss the efficacy of biomarkers to detect senescence within different skin compartments and cell types, and how they may contribute to myriad manifestations of skin aging and age-related skin pathologies.
Insights
Cellular senescence, a state of irreversible cell growth arrest, contributes to aging. Identifying reliable biomarkers for senescent cells in skin is crucial for understanding and treating age-related skin conditions.
Area of Science:
- Cellular and Molecular Biology
- Dermatology
- Gerontology
Background:
- Cellular senescence is a permanent cell cycle arrest triggered by various stressors, impacting tissue aging and disease.
- Senescent cells accumulate in aged tissues, including skin, and are implicated in age-related changes and pathologies.
- A universal biomarker for senescent cells is lacking, hindering research in aging and disease.
Purpose of the Study:
- To review current biomarkers for detecting senescent cells.
- To evaluate the utility of these biomarkers in the context of skin aging.
- To discuss biomarker efficacy across different skin compartments and cell types.
Main Methods:
- Literature review of existing senescent cell biomarkers.
- Analysis of biomarker applicability in skin aging research.
- Discussion of senescent cell detection in various skin contexts.
Main Results:
- Senescent cells are present in both chronological and photoaged skin.
- Various biomarkers exist for senescent cell detection, each with specific applications.
- Biomarker efficacy varies depending on the skin compartment and cell type studied.
Conclusions:
- Senescent cells play a role in skin aging and associated pathologies.
- Effective biomarkers are essential for quantifying senescent cells in skin.
- Further research is needed to optimize biomarker use for understanding skin aging.
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