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.

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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

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article

Dual Bcl-2/Bcl-xl inhibition via AZD0466 combines with immune checkpoint blockade to enhance anti-tumour activity

Deanna A. Mele, Andrea Newbold, Peter Fraser, Ricky W. Johnstone et al.
Cell Death and Disease
Cancer Immunotherapy and Biomarkers
article

Dual Bcl-2/Bcl-xl inhibition via AZD0466 combines with immune checkpoint blockade to enhance anti-tumour activity

Deanna A. Mele, Andrea Newbold, Peter Fraser, Ricky W. Johnstone, Leonie A. Cluse, Courtney L. Andersen, Dane M. Newman, Luyao Kevin Xu, Benjamin W. C. Legg
article en

Abstract

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.

Cell Death and DiseaseVol. 17(1)
The University of Melbourne (AU), Peter MacCallum Cancer Centre (AU), AstraZeneca (South Korea) (KR), AstraZeneca (Brazil) (BR), AstraZeneca (United States) (US)
Australian Cancer Research Foundation, Peter MacCallum Cancer Centre, Kids' Cancer Project, Peter MacCallum Foundation, Medical Research Council, National Health and Medical Research Council
Good health and well-being
Openalex Percentile: Top 97%
Cancer Immunotherapy and Biomarkers
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