Dual Bcl-2/Bcl-xl inhibition via AZD0466 combines with immune checkpoint blockade to enhance anti-tumour activity
Small molecule inhibitors designed to specifically target oncogenic proteins have demonstrated potent anti-tumour activities due to direct effects on tumour cells survival and/or proliferation. However, the effects of these compounds on normal cells, specifically immune cells and their potential to impede or enhance anti-cancer immunotherapies has yet to be fully explored. Using an in vitro co-culture system to assess CD8+ T cell killing of tumour cells, we identified compounds that inhibit Bcl-2 and Bcl-xl as agents that can induce tumour cell death without impacting the differentiation or function of anti-tumour T cells. Accordingly, in vivo treatment of mice bearing solid tumours with a combination of the Bcl-2/Bcl-xl inhibitor AZD0466 and anti-PD-L1 immunotherapy resulted in enhanced anti-tumour effects and improved survival compared to equivalent monotherapies.
Authors
- Deanna A. Mele (ORCID: https://orcid.org/0000-0002-6429-4269)
- Andrea Newbold (ORCID: https://orcid.org/0000-0002-0481-2431)
- Peter Fraser (ORCID: https://orcid.org/0000-0002-0041-1227)
- Ricky W. Johnstone (ORCID: https://orcid.org/0000-0001-7053-9237)
- Leonie A. Cluse (ORCID: https://orcid.org/0000-0001-8613-0508)
- Courtney L. Andersen (ORCID: https://orcid.org/0000-0003-2064-2273)
- Dane M. Newman
- Luyao Kevin Xu
- Benjamin W. C. Legg
Institutions
- The University of Melbourne (AU)
- Peter MacCallum Cancer Centre (AU)
- AstraZeneca (South Korea) (KR)
- AstraZeneca (Brazil) (BR)
- AstraZeneca (United States) (US)
Publication Details
- Journal
- Cell Death and Disease
- Published
- 2026-01-06
- DOI
- https://doi.org/10.1038/s41419-025-08354-w
- Primary Topic
- Cancer Immunotherapy and Biomarkers
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Australian Cancer Research Foundation
- Peter MacCallum Cancer Centre
- Kids' Cancer Project
- Peter MacCallum Foundation
- Medical Research Council
- National Health and Medical Research Council