Aging and TOR: interwoven in the fabric of life

Zelton Dave Sharp1

  • 1Department of Molecular Medicine, Institute of Biotechnology, University of Texas Health Science Center San Antonio, San Antonio, TX, 78245, USA. sharp@uthscsa.edu

Insights

Retarding aging to enhance healthspan is achievable by targeting the nutrient-sensing pathway, the target of rapamycin (TOR). Inhibiting TOR extends lifespan across species, suggesting conserved aging mechanisms.

Area of Science:

  • Aging research
  • Cellular biology
  • Metabolic pathways

Background:

  • Calorie restriction and growth factor restriction have long been known to extend lifespan.
  • Recent drug interventions targeting aging pathways show promise.
  • The target of rapamycin (TOR) pathway is a key regulator of cellular responses.

Purpose of the Study:

  • To explore the role of the target of rapamycin (TOR) pathway in aging.
  • To investigate the potential of retarding aging for improving healthspan in older individuals.

Main Methods:

  • Review of longstanding results from calorie and growth factor restriction studies.
  • Analysis of recent findings on interventional drugs targeting aging.
  • Examination of the conserved nature of TOR pathway's role in lifespan extension.

Main Results:

  • Evidence suggests retarding aging to improve quality of life is feasible.
  • The target of rapamycin (TOR) pathway is central to cellular responses to nutrients, growth factors, and stress.
  • Inhibiting TOR activity leads to conserved life-extending responses from yeast to mammals.

Conclusions:

  • Targeting the TOR pathway represents a promising strategy for interventions aimed at improving healthspan.
  • The conserved nature of TOR's role in aging suggests a fundamental biological mechanism.
  • Aging may have evolved to prioritize reproductive potential in younger organisms.

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