Open access · CC-BY
via OpenAlex
Senescence under appraisal: hopes and challenges revisited
Camilla S. A. Davan-Wetton, Emanuela Pessolano, Mauro Perretti, Trinidad Montero‐Melendez
Cellular and Molecular Life Sciences · 2021 · ▲ 58 citations
Cellular senescence
Altered intercellular communication
Chronic inflammation
Senolytics
Human
Review
Abstract
In recent years, cellular senescence(definition) has become the focus of attention in multiple areas of biomedical research. Typically defined as an irreversible cell cycle arrest accompanied by increased cellular growth, metabolic activity and by a characteristic messaging secretome, cellular senescence can impact on multiple physiological and pathological processes such as wound healing, fibrosis, cancer and ageing. These unjustly called 'zombie cells' are indeed a rich source of opportunities for innovative therapeutic development. In this review, we collate the current understanding of the process of cellular senescence and its two-faced nature, i.e. beneficial/detrimental, and reason this duality is linked to contextual aspects. We propose the senescence programme as an endogenous pro-resolving mechanism that may lead to sustained inflammation and damage when dysregulated or when senescent cells are not cleared efficiently. This pro-resolving model reconciles the paradoxical two faces of senescence by emphasising that it is the unsuccessful completion of the programme, and not senescence itself, what leads to pathology. Thus, pro-senescence therapies under the right context, may favour inflammation resolution. We also review the evidence for the multiple therapeutic approaches under development based on senescence, including its induction, prevention, clearance and the use of senolytic and senomorphic drugs. In particular, we highlight the importance of the immune system in the favourable outcome of senescence and the implications of an inefficient immune surveillance in completion of the senescent cycle. Finally, we identify and discuss a number of challenges and existing gaps to encourage and stimulate further research in this exciting and unravelled field, with the hope of promoting and accelerating the clinical success of senescence-based therapies.
◌ CITATION ONLY
Full text is not openly licensed for redistribution here. Read it at the source:
Provenance
- Source
- OpenAlex
- DOI
- 10.1007/s00018-020-03746-x
- Canonical
- link ↗
- Fetched
- 2026-06-29 MST
Cite this
APA
Davan-Wetton, C.S.A., Pessolano, E., Perretti, M., & Montero‐Melendez, T. (2021). Senescence under appraisal: hopes and challenges revisited. <em>Cellular and Molecular Life Sciences</em>. https://doi.org/10.1007/s00018-020-03746-x
Vancouver
Davan-Wetton CSA, Pessolano E, Perretti M, Montero‐Melendez T. Senescence under appraisal: hopes and challenges revisited. Cellular and Molecular Life Sciences. 2021. doi:10.1007/s00018-020-03746-x.
BibTeX
@article{camilla2021Senesc,
title = {Senescence under appraisal: hopes and challenges revisited},
author = {Camilla S. A. Davan-Wetton and Emanuela Pessolano and Mauro Perretti and Trinidad Montero‐Melendez},
journal = {Cellular and Molecular Life Sciences},
year = {2021},
doi = {10.1007/s00018-020-03746-x},
}
Research neighborhood
References, citing works, and semantically nearest findings. Click a node to open it.
Related findings
Advances in Therapy 2020
Open access · CC-BY
Cellular Senescence as a Therapeutic Target for Age-Related Diseases: A Review
Nature Reviews Drug Discovery 2024
Open access · CC-BY
Senescence as a therapeutic target in cancer and age-related diseases
International Journal of Molecular Sciences 2024
Open access · CC-BY
Genetic and Epigenetic Interactions Involved in Senescence of Stem Cells
Biomolecules 2025
Open access · CC-BY
Targeting Senescence: A Review of Senolytics and Senomorphics in Anti-Aging Interventions
Cold Spring Harbor Symposia on Quantitative Biology 2008
Open access · OA
Implications of Cellular Senescence in Tissue Damage Response, Tumor Suppression, and Stem Cell Biology
Cancer Research and Treatment 2009
Open access · OA