Senotherapeutics: Targeting senescent cells for the main age-related diseases

Virginia Boccardi1, Patrizia Mecocci1

  • 1Santa Maria della Misericordia Hospital, Section of Gerontology and Geriatrics, Department of Medicine and Surgery, University of Perugia, Italy.

Insights

Targeting senescent cells with senotherapeutics shows promise for reducing age-related diseases. Natural compounds may offer safer anti-aging benefits, but more research is needed on their mechanisms and potential side effects.

Area of Science:

  • Gerontology and Cellular Biology
  • Pharmacology and Therapeutics

Background:

  • Cellular senescence plays a key role in aging and age-related diseases like Alzheimer's, atherosclerosis, and type 2 diabetes.
  • Senescent cells accumulate with age, contributing to tissue dysfunction and disease pathogenesis.

Purpose of the Study:

  • To review current knowledge on targeting senescent cells to mitigate age-related diseases.
  • To discuss senotherapeutic strategies, including senolytics and senomorphics, in preclinical and clinical studies.

Main Methods:

  • Literature review of animal models and human studies on cellular senescence and senotherapeutics.
  • Analysis of molecules with anti-senescence activities, including synthetic agents and natural compounds.
  • Evaluation of safety and efficacy data from clinical trials of senotherapeutics.

Main Results:

  • Senotherapeutic approaches show potential for translation to human therapies against aging and related diseases.
  • Numerous molecules, both synthetic and natural, are being investigated for their senotherapeutic properties.
  • Clinical trials indicate growing interest and initial positive findings for senotherapeutics.

Conclusions:

  • Targeting cellular senescence is a promising strategy for combating age-related diseases.
  • Natural senolytic compounds may offer a safer alternative with lower toxicity for human application.
  • Further research is required to define mechanisms of action and ensure the safety of senolytic agents.

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