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dc.contributor.authorDavan-Wetton, CSA
dc.contributor.authorPessolano, E
dc.contributor.authorPerretti, M
dc.contributor.authorMontero-Melendez, T
dc.date.accessioned2021-01-20T18:25:24Z
dc.date.available2020-12-17
dc.date.available2021-01-20T18:25:24Z
dc.date.issued2021-01-13
dc.identifier.citationDavan-Wetton, C.S.A., Pessolano, E., Perretti, M. et al. Senescence under appraisal: hopes and challenges revisited. Cell. Mol. Life Sci. (2021). https://doi.org/10.1007/s00018-020-03746-xen_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/69892
dc.description.abstractIn recent years, cellular senescence 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.en_US
dc.languageeng
dc.publisherSpringer Natureen_US
dc.relation.ispartofCell Mol Life Sci
dc.rightsThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
dc.subjectAgeingen_US
dc.subjectCanceren_US
dc.subjectResolution of inflammationen_US
dc.subjectSenescenceen_US
dc.subjectSenolyticsen_US
dc.subjectTissue repairen_US
dc.titleSenescence under appraisal: hopes and challenges revisited.en_US
dc.typeArticleen_US
dc.rights.holder© The Author(s) 2021
dc.identifier.doi10.1007/s00018-020-03746-x
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/33439271en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
pubs.publisher-urlhttp://doi.org/10.1007/s00018-020-03746-x
dcterms.dateAccepted2020-12-17
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US
qmul.funderTranslating the Resolution of Inflammation: MC3 in human arthritis synovia::Medical Research Councilen_US
qmul.funderTranslating the Resolution of Inflammation: MC3 in human arthritis synovia::Medical Research Councilen_US


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