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The emerging role of targeted protein degradation to treat and study cancer
Maximillian H Brodermann1, Elizabeth K Henderson1, Rob S Sellar1
1Department of Haematology, UCL Cancer Institute, University College London, London, UK.
Abstract:
The evolution of cancer treatment has provided increasingly targeted strategies both in the upfront and relapsed disease settings. Small-molecule inhibitors and immunotherapy have risen to prominence with chimeric antigen receptor T-cells, checkpoint inhibitors, kinase inhibitors, and monoclonal antibody therapies being deployed across a range of solid organ and haematological malignancies. However, novel approaches are required to target transcription factors and oncogenic fusion proteins that are central to cancer biology and have generally eluded successful drug development. Thalidomide analogues causing protein degradation have been a cornerstone of treatment in multiple myeloma, but a lack of in-depth mechanistic understanding initially limited progress in the field. When the protein cereblon (CRBN) was found to mediate thalidomide analogues' action and CRBN's neo-targets were identified, existing and novel drug development accelerated, with applications outside multiple myeloma, including non-Hodgkin's lymphoma, myelodysplastic syndrome, and acute leukaemias. Critically, transcription factors were the first canonical targets described. In addition to broadening the application of protein-degrading drugs, resistance mechanisms are being overcome and targeted protein degradation is widening the scope of druggable proteins against which existing approaches have been ineffective. Examples of targeted protein degraders include molecular glues and proteolysis targeting chimeras (PROTACs): heterobifunctional molecules that bind to proteins of interest and cause proximity-induced ubiquitination and proteasomal degradation via a linked E3 ligase. Twenty years since their inception, PROTACs have begun progressing through clinical trials, with early success in targeting the oestrogen receptor and androgen receptor in breast and prostate cancer respectively. This review explores important developments in targeted protein degradation to both treat and study cancer. It also considers the potential advantages and challenges in the translational aspects of developing new treatments. © 2024 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.
Insights
Targeted protein degradation, including molecular glues and proteolysis targeting chimeras (PROTACs), offers novel cancer treatment strategies by degrading previously undruggable proteins like transcription factors. These advancements are expanding therapeutic options and overcoming resistance mechanisms in various cancers.
Area of Science:
- Oncology and Molecular Biology
- Drug Discovery and Development
- Biochemistry
Background:
- Cancer treatment has evolved with targeted therapies like immunotherapy and small-molecule inhibitors.
- Transcription factors and oncogenic fusion proteins remain challenging targets for conventional drug development.
- Thalidomide analogues demonstrated the potential of protein degradation, with cereblon (CRBN) identified as a key mediator.
Purpose of the Study:
- To review recent advancements in targeted protein degradation for cancer treatment and research.
- To explore the mechanisms and applications of molecular glues and proteolysis targeting chimeras (PROTACs).
- To discuss the translational potential, advantages, and challenges of developing targeted protein degraders.
Main Methods:
- Review of scientific literature on targeted protein degradation in cancer.
- Analysis of mechanisms involving molecular glues and PROTACs.
- Examination of clinical trial progress and therapeutic applications.
Main Results:
- Targeted protein degradation, utilizing molecular glues and PROTACs, effectively degrades proteins previously considered undruggable.
- CRBN's role has accelerated drug development, expanding applications beyond multiple myeloma to other hematological malignancies and solid tumors.
- PROTACs are progressing in clinical trials, showing early success in targeting hormone receptors in breast and prostate cancers.
Conclusions:
- Targeted protein degradation represents a significant paradigm shift in cancer therapy, offering new avenues for treating resistant and previously intractable malignancies.
- Further research into mechanisms and overcoming resistance is crucial for maximizing the clinical benefit of these novel agents.
- PROTACs and molecular glues hold immense promise for expanding the scope of druggable targets and improving patient outcomes in oncology.
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