The interplay between FOXO3 and FOXM1 influences sensitivity to AKT inhibition in PIK3CA and PIK3CA/PTEN altered estrogen receptor positive breast cancer

Loss of PTEN expression, via homozygous or hemizygous deletion, is common in PIK3CA mutant ER + BC tumors. We assessed reduction of PTEN protein expression on AKT inhibitor capivasertib efficacy in PIK3CA altered tumors. In PIK3CA altered, PTEN protein high models, PI3Kα and AKT inhibition was effective, however ablation and partial PTEN expression reduction attenuated PI3Kαi but not AKTi efficacy, alone or combined with fulvestrant. Efficacy was FOXO3 dependent and associated with FOXM1 downregulation. FOXO3A deletion reduced response to capivasertib, and increased FOXM1 expression. Long term capivasertib exposure of ER+ BC cells upregulated FOXM1 expression. Downregulating FOXM1 expression reversed resistance to capivasertib, while FOXM1 overexpression reduced capivasertib efficacy. Collectively this suggests the AKT-FOXO3-FOXM1 axis plays a pivotal role in response to AKTi in ER+ breast cancer with PIK3CA mutations with and without expression of PTEN, that FOXO3 expression loss can mediate resistance, and that FOXM1 downregulation is a potential biomarker of response.

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Publication Details

Journal
npj Breast Cancer
Published
2025-04-22
DOI
https://doi.org/10.1038/s41523-025-00752-9
Citations
1
Primary Topic
PI3K/AKT/mTOR signaling in cancer
Type
article
Field-Weighted Citation Impact
0.81

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article

The interplay between FOXO3 and FOXM1 influences sensitivity to AKT inhibition in PIK3CA and PIK3CA/PTEN altered estrogen receptor positive breast cancer

Brandon S. Willis, Eleanor M. Wigmore, Ming Li Chia, Sophie D’Arcy et al.
1 citations
npj Breast Cancer
PI3K/AKT/mTOR signaling in cancer
0.81
article

The interplay between FOXO3 and FOXM1 influences sensitivity to AKT inhibition in PIK3CA and PIK3CA/PTEN altered estrogen receptor positive breast cancer

Brandon S. Willis, Eleanor M. Wigmore, Ming Li Chia, Sophie D’Arcy, Catherine Blaker, Kevin Michael Brindle, Cath Eberlein, Stuart C. Williamson, Lambert Montava‐Garriga, Amanda L. Christie, Lauren Bradshaw, Valentina Cutano, Simon T. Barry, Susan E. Critchlow, Lorna Hopcroft, Elza C. de Bruin, Susana R�os, Rhys Fox, James Kerr, Jenny Ashforth
article en
1 citations

Abstract

Loss of PTEN expression, via homozygous or hemizygous deletion, is common in PIK3CA mutant ER + BC tumors. We assessed reduction of PTEN protein expression on AKT inhibitor capivasertib efficacy in PIK3CA altered tumors. In PIK3CA altered, PTEN protein high models, PI3Kα and AKT inhibition was effective, however ablation and partial PTEN expression reduction attenuated PI3Kαi but not AKTi efficacy, alone or combined with fulvestrant. Efficacy was FOXO3 dependent and associated with FOXM1 downregulation. FOXO3A deletion reduced response to capivasertib, and increased FOXM1 expression. Long term capivasertib exposure of ER+ BC cells upregulated FOXM1 expression. Downregulating FOXM1 expression reversed resistance to capivasertib, while FOXM1 overexpression reduced capivasertib efficacy. Collectively this suggests the AKT-FOXO3-FOXM1 axis plays a pivotal role in response to AKTi in ER+ breast cancer with PIK3CA mutations with and without expression of PTEN, that FOXO3 expression loss can mediate resistance, and that FOXM1 downregulation is a potential biomarker of response.

npj Breast CancerVol. 11(1)
AstraZeneca (United Kingdom) (GB), Cancer Research UK Cambridge Center (GB), AstraZeneca (Singapore) (SG), AstraZeneca (United States) (US), AstraZeneca (Germany) (DE)
AstraZeneca
Good health and well-being
Openalex Percentile: Top 29%
PI3K/AKT/mTOR signaling in cancer
0.81
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