Gamma Secretase Inhibitors in Cancer: A Current Perspective on Clinical Performance

Tyler R McCaw1, Evelyn Inga1, Herbert Chen2

  • 1Divisions of Surgical Oncology, The University of Alabama at Birmingham, Birmingham, Alabama, USA.

The Oncologist
|December 7, 2020
PubMed

Insights

Gamma secretase inhibitors (GSIs) show promise in preclinical cancer models but have limited clinical success. Further research is needed to optimize their use in combination therapies for better cancer control.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cancer Therapeutics

Background:

  • Gamma secretase inhibitors (GSIs) target Notch receptor cleavage, initially for Alzheimer's disease, and show anticancer potential in preclinical studies.
  • GSIs induce cancer stem-like cell differentiation, apoptosis, inhibit epithelial-to-mesenchymal transition, and sensitize cells to chemoradiotherapy.

Purpose of the Study:

  • To review the current understanding of GSI mechanisms in cancer.
  • To discuss the clinical performance of GSIs in various solid tumors.
  • To identify future research areas for optimizing GSI utility in cancer treatment.

Main Methods:

  • Review of preclinical data and clinical trial outcomes for GSIs in cancer.
  • Analysis of GSI mechanisms, including effects on Notch signaling and immune responses.
  • Exploration of compensatory pathways and combinatorial strategies.

Main Results:

  • GSIs have shown significant promise in preclinical cancer models but have largely failed to demonstrate clinical benefit in solid tumors, except for CNS malignancies and desmoid tumors.
  • Disappointing clinical performance highlights unanswered questions regarding GSI impact on antitumor immunity and the need to target compensatory pathways.

Conclusions:

  • Optimizing GSI therapy requires addressing limitations in understanding their mechanisms and clinical effects.
  • Future investigations should focus on rational incorporation of GSIs into combinatorial strategies to improve outcomes in Notch-dependent cancers.