Defining Splicing Factor Requirements for Androgen Receptor Variant Synthesis in Advanced Prostate Cancer
Resistance to androgen receptor (AR)-targeted therapies represents a major challenge in prostate cancer. A key mechanism of treatment resistance in patients who progress to castration-resistant prostate cancer (CRPC) is the generation of alternatively spliced AR variants (AR-V). Unlike full-length AR isoforms, AR-Vs are constitutively active and refractory to current receptor-targeting agents and hence drive tumor progression. Identifying regulators of AR-V synthesis may therefore provide new therapeutic opportunities in combination with conventional AR-targeting agents. Our understanding of AR transcript splicing, and the factors that control the synthesis of AR-Vs, remains limited. Although candidate-based approaches have identified a small number of AR-V splicing regulators, an unbiased analysis of splicing factors important for AR-V generation is required to fill an important knowledge gap and furnish the field with novel and tractable targets for prostate cancer treatment. To that end, we conducted a bespoke CRISPR screen to profile splicing factor requirements for AR-V synthesis. MFAP1 and CWC22 were shown to be required for the generation of AR-V mRNA transcripts, and their depletion resulted in reduced AR-V protein abundance and cell proliferation in several CRPC models. Global transcriptomic analysis of MFAP1-depleted cells revealed both AR-dependent and -independent transcriptional impacts, including genes associated with DNA damage response. As such, MFAP1 downregulation sensitized prostate cancer cells to ionizing radiation, suggesting that therapeutically targeting AR-V splicing could provide novel cellular vulnerabilities which can be exploited in CRPC. Implications: We have utilized a CRISPR screening approach to identify key regulators of pathogenic AR splicing in prostate cancer.
Authors
- Dominic Jones
- Nicholas Brittain
- R. Scott Duncan
- Sara Luzzi (ORCID: https://orcid.org/0000-0001-6337-7495)
- Beth Adamson (ORCID: https://orcid.org/0009-0006-8102-0135)
- Claire Crafter (ORCID: https://orcid.org/0000-0001-6566-0868)
- Luke Gaughan
- S Peel (ORCID: https://orcid.org/0000-0001-9850-1409)
- Laura Walker (ORCID: https://orcid.org/0000-0002-5298-924X)
- Lewis Chaytor
- Hannah Kendall (ORCID: https://orcid.org/0009-0001-2539-585X)
- Daniel O’Neill (ORCID: https://orcid.org/0009-0006-3424-7214)
Institutions
- AstraZeneca (United Kingdom) (GB)
- Centre for Life (GB)
- Pierre Fabre (United Kingdom) (GB)
- AstraZeneca (Singapore) (SG)
- Newcastle upon Tyne Hospital (GB)
- AstraZeneca (Spain) (ES)
- Newcastle University (GB)
Publication Details
- Journal
- Molecular Cancer Research
- Published
- 2024-09-30
- DOI
- https://doi.org/10.1158/1541-7786.mcr-23-0958
- Citations
- 4
- Primary Topic
- Prostate Cancer Treatment and Research
- Type
- article
- Field-Weighted Citation Impact
- 1.68
Funders
- JGW Patterson Foundation
- Cancer Research UK
- Medical Research Council
- Biotechnology and Biological Sciences Research Council
- European Regional Development Fund