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.
Abstract:
Gamma secretase inhibitors (GSIs), initially developed as Alzheimer's therapies, have been repurposed as anticancer agents given their inhibition of Notch receptor cleavage. The success of GSIs in preclinical models has been ascribed to induction of cancer stem-like cell differentiation and apoptosis, while also impairing epithelial-to-mesenchymal transition and sensitizing cells to traditional chemoradiotherapies. The promise of these agents has yet to be realized in the clinic, however, as GSIs have failed to demonstrate clinical benefit in most solid tumors with the notable exceptions of CNS malignancies and desmoid tumors. Disappointing clinical performance to date reflects important questions that remain to be answered. For example, what is the net impact of these agents on antitumor immune responses, and will they require concurrent targeting of tumor-intrinsic compensatory pathways? Addressing these limitations in our current understanding of GSI mechanisms will undoubtedly facilitate their rational incorporation into combinatorial strategies and provide a valuable tool with which to combat Notch-dependent cancers. In the present review, we provide a current understanding of GSI mechanisms, discuss clinical performance to date, and suggest areas for future investigation that might maximize the utility of these agents. IMPLICATIONS FOR PRACTICE: The performance of gamma secretase inhibitors (GSIs) in clinical trials generally has not reflected their encouraging performance in preclinical studies. This review provides a current perspective on the clinical performance of GSIs across various solid tumor types alongside putative mechanisms of antitumor activity. Through exploration of outstanding gaps in knowledge as well as reasons for success in certain cancer types, the authors identify areas for future investigation that will likely enable incorporation of GSIs into rational combinatorial strategies for superior tumor control and patient outcomes.
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.
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