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MDM2 Inhibitors for Cancer Therapy: The Past, Present, and Future
Wei Wang1, Najah Albadari2, Yi Du2
1Department of Pharmacological and Pharmaceutical Sciences, College of Pharmacy (W.W., Y.D., J.F.F., H.T.S., R.Z.), Drug Discovery Institute (W.W., R.Z.), Stem Cell Center, Department of Biology and Biochemistry (W.X., F.M.), University of Houston, Houston, Texas; College of Pharmacy, University of Tennessee Health Science Center, Memphis, Tennessee (N.A., W.L.); and Chemical Biology Program, Department of Pharmacology and Toxicology, University of Texas Medical Branch, Galveston, Texas (J.Z.) wwang4@central.uh.edu rzhang27@central.uh.edu.
Abstract:
Since its discovery over 35 years ago, MDM2 has emerged as an attractive target for the development of cancer therapy. MDM2's activities extend from carcinogenesis to immunity to the response to various cancer therapies. Since the report of the first MDM2 inhibitor more than 30 years ago, various approaches to inhibit MDM2 have been attempted, with hundreds of small-molecule inhibitors evaluated in preclinical studies and numerous molecules tested in clinical trials. Although many MDM2 inhibitors and degraders have been evaluated in clinical trials, there is currently no Food and Drug Administration (FDA)-approved MDM2 inhibitor on the market. Nevertheless, there are several current clinical trials of promising agents that may overcome the past failures, including agents granted FDA orphan drug or fast-track status. We herein summarize the research efforts to discover and develop MDM2 inhibitors, focusing on those that induce MDM2 degradation and exert anticancer activity, regardless of the p53 status of the cancer. We also describe how preclinical and clinical investigations have moved toward combining MDM2 inhibitors with other agents, including immune checkpoint inhibitors. Finally, we discuss the current challenges and future directions to accelerate the clinical application of MDM2 inhibitors. In conclusion, targeting MDM2 remains a promising treatment approach, and targeting MDM2 for protein degradation represents a novel strategy to downregulate MDM2 without the side effects of the existing agents blocking p53-MDM2 binding. Additional preclinical and clinical investigations are needed to finally realize the full potential of MDM2 inhibition in treating cancer and other chronic diseases where MDM2 has been implicated. SIGNIFICANCE STATEMENT: Overexpression/amplification of the MDM2 oncogene has been detected in various human cancers and is associated with disease progression, treatment resistance, and poor patient outcomes. This article reviews the previous, current, and emerging MDM2-targeted therapies and summarizes the preclinical and clinical studies combining MDM2 inhibitors with chemotherapy and immunotherapy regimens. The findings of these contemporary studies may lead to safer and more effective treatments for patients with cancers overexpressing MDM2.
Insights
Targeting MDM2 (mouse double minute 2 homolog) shows promise for cancer therapy by inducing protein degradation. Research explores MDM2 inhibitors, including combinations with immunotherapy, to overcome treatment resistance and improve patient outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Drug Discovery
Background:
- MDM2 (mouse double minute 2 homolog) oncogene overexpression is linked to cancer progression, treatment resistance, and poor outcomes.
- Despite decades of research, no MDM2 inhibitor is FDA-approved, though many candidates show promise.
Purpose of the Study:
- To review research on MDM2 inhibitors, focusing on those inducing MDM2 degradation for anticancer activity.
- To explore the combination of MDM2 inhibitors with other therapies, including immune checkpoint inhibitors.
- To discuss challenges and future directions for MDM2-targeted cancer therapies.
Main Methods:
- Review of preclinical and clinical studies on MDM2 inhibitors and degraders.
- Analysis of therapeutic strategies involving MDM2 inhibition, including combination therapies.
- Examination of challenges and future prospects in MDM2-targeted drug development.
Main Results:
- MDM2 inhibitors, particularly those inducing protein degradation, demonstrate anticancer potential irrespective of p53 status.
- Combination strategies, including with chemotherapy and immunotherapy, are advancing clinical investigations.
- Promising agents have received FDA orphan drug or fast-track designations, indicating potential to overcome past failures.
Conclusions:
- Targeting MDM2, especially through protein degradation, offers a novel strategy for cancer treatment with potentially fewer side effects than current agents.
- Further preclinical and clinical research is crucial to fully realize the therapeutic potential of MDM2 inhibition in cancer and other diseases.
- MDM2-targeted therapies hold promise for developing safer and more effective treatments for cancers with MDM2 overexpression.
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