A Critical Appraisal of the Utility of Targeting Therapy-Induced Senescence for Cancer Treatment

Tareq Saleh1,2, Edward F Greenberg3, Anthony C Faber4,5,6

  • 1Department of Pharmacology and Therapeutics, College of Medicine and Health Sciences, Arabian Gulf University, Manama, Bahrain.

Cancer Research
|March 4, 2025
PubMed

Insights

Senolytic compounds eliminate senescent cells, potentially improving cancer therapy. Preclinical studies show promise, but further research is needed for clinical translation and safe, effective senolytic agents.

Area of Science:

  • Oncology
  • Gerontology
  • Pharmacology

Background:

  • Cancer treatments like chemotherapy and radiotherapy often leave behind senescent tumor cells.
  • These senescent cells can promote tumor growth and suppress the immune system, potentially leading to recurrence.
  • Senolytics, which clear senescent cells, are being investigated to improve cancer treatment outcomes.

Purpose of the Study:

  • To review preclinical literature on senolytics as an adjunct cancer therapy.
  • To discuss limitations of current preclinical models for senolytic research.
  • To provide perspectives on the clinical development of senolytics in cancer treatment.

Main Methods:

  • Review of recent preclinical studies on senolytic compounds in cancer treatment.
  • Analysis of the role of therapy-induced senescence in cancer recurrence.
  • Evaluation of senolytic agents' potential for enhancing conventional cancer therapies.

Main Results:

  • Preclinical evidence suggests senolytics can enhance the efficacy of standard cancer therapies.
  • Senolytics show potential in prolonging the antitumor activity of senescence-inducing treatments.
  • Current preclinical models have limitations in fully assessing senolytic efficacy and safety.

Conclusions:

  • Senolytics hold promise as an adjunct therapy to improve cancer treatment efficacy and prolong antitumor effects.
  • Further development of senolytic agents with optimal properties for clinical testing is crucial.
  • Addressing tolerability and activity in therapy-induced senescence is key for successful clinical translation.

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