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A second generation of senotherapies: the development of targeted senolytics, senoblockers and senoreversers for healthy ageing.
Dhokia, Vinesh; Albati, Amal; Smith, Hannah; Thomas, Gethin; Macip, Salvador.
Afiliação
  • Dhokia V; Mechanisms of Cancer and Ageing Laboratory, Barcelona, Spain.
  • Albati A; Department of Molecular and Cell Biology, University of Leicester, Leicester, U.K.
  • Smith H; Mechanisms of Cancer and Ageing Laboratory, Barcelona, Spain.
  • Thomas G; Department of Molecular and Cell Biology, University of Leicester, Leicester, U.K.
  • Macip S; Mechanisms of Cancer and Ageing Laboratory, Barcelona, Spain.
Biochem Soc Trans ; 2024 Jun 28.
Article em En | MEDLINE | ID: mdl-38940746
ABSTRACT
Cellular senescence, a form of terminal cell cycle arrest, is as a key driver of organismal ageing and an important factor in age-related diseases. Insights into the senescent phenotype have led to the development of novel therapeutic strategies, collectively known as senotherapies, that aim to ameliorate the detrimental effects of senescent cell accumulation in tissues. The senotherapeutic field has rapidly evolved over the past decade, with clinical translation of the first drugs discovered currently underway. What began as the straightforward removal of senescent cells using repurposed compounds, which were given the name of senolytics, has grown into an expanding field that uses different state of the art approaches to achieve the goal of preventing the build-up of senescent cells in the body. Here, we summarize the emergence of a new generation of senotherapies, based on improving the efficacy and safety of the original senolytics by making them targeted, but also branching out into drugs that prevent senescence (senoblockers) or revert it (senoreversers).The use of nanotechnology, specific antibodies, cell-based approaches and restored immunosurveillance is likely to revolutionize the field of senotherapies in the near future, hopefully allowing it to realize its full clinical potential.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article