The oestrous cycle stage affects mammary tumour sensitivity to chemotherapy

The response of breast cancer to neoadjuvant chemotherapy (NAC) varies substantially, even when tumours belong to the same molecular or histological subtype<sup>1</sup>. Here we identify the oestrous cycle as an important contributor to this heterogeneity. In three mouse models of breast cancer, we show reduced responses to NAC when treatment is initiated during the dioestrus stage, when compared with initiation during the oestrus stage. Similar findings were observed in retrospective premenopausal cohorts of human patients. Mechanistically, the dioestrus stage exhibits systemic and localized changes, including (1) an increased number of cells undergoing epithelial-to-mesenchymal transition linked to chemoresistance<sup>2-4</sup> and (2) decreased tumour vessel diameter, suggesting potential constraints to drug sensitivity and delivery. In addition, an elevated presence of macrophages, previously associated with chemoresistance induction<sup>5</sup>, characterizes the dioestrus phase. Whereas NAC disrupts the oestrous cycle, this elevated macrophage prevalence persists and depletion of macrophages mitigates the reduced therapy response observed when initiating treatment during dioestrus. Our data collectively demonstrate the oestrous cycle as a crucial infradian rhythm determining chemosensitivity, warranting future clinical studies to exploit optimal treatment initiation timing for enhanced chemotherapy outcomes.

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Publication Details

Journal
Nature
Published
2024-12-04
DOI
https://doi.org/10.1038/s41586-024-08276-1
Citations
13
Primary Topic
Cancer Cells and Metastasis
Type
article
Field-Weighted Citation Impact
3.67
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article

The oestrous cycle stage affects mammary tumour sensitivity to chemotherapy

Marieke van de Ven, Lennart J. van Winden, Laura Bornes, Natalie Proost et al.
13 citations
Nature
Cancer Cells and Metastasis
3.67
article

The oestrous cycle stage affects mammary tumour sensitivity to chemotherapy

Marieke van de Ven, Lennart J. van Winden, Laura Bornes, Natalie Proost, Marika Caruso, Jelle Wesseling, Judith R. Kroep, Huub H. van Rossum, Nadia de Gruil, Jeroen Lohuis, Annegien Broeks, Manon Boeije, Colinda L. G. J. Scheele, Renée X. de Menezes, Jacco van Rheenen, Sabine C. Linn, Marleen Kok, Guillaume Belthier, Mirthe Lanfermeijer, Beaunelle de Bruijn, Leyla Azarang, Veerle Geurts, E Delgado
article en
13 citations

Abstract

The response of breast cancer to neoadjuvant chemotherapy (NAC) varies substantially, even when tumours belong to the same molecular or histological subtype<sup>1</sup>. Here we identify the oestrous cycle as an important contributor to this heterogeneity. In three mouse models of breast cancer, we show reduced responses to NAC when treatment is initiated during the dioestrus stage, when compared with initiation during the oestrus stage. Similar findings were observed in retrospective premenopausal cohorts of human patients. Mechanistically, the dioestrus stage exhibits systemic and localized changes, including (1) an increased number of cells undergoing epithelial-to-mesenchymal transition linked to chemoresistance<sup>2-4</sup> and (2) decreased tumour vessel diameter, suggesting potential constraints to drug sensitivity and delivery. In addition, an elevated presence of macrophages, previously associated with chemoresistance induction<sup>5</sup>, characterizes the dioestrus phase. Whereas NAC disrupts the oestrous cycle, this elevated macrophage prevalence persists and depletion of macrophages mitigates the reduced therapy response observed when initiating treatment during dioestrus. Our data collectively demonstrate the oestrous cycle as a crucial infradian rhythm determining chemosensitivity, warranting future clinical studies to exploit optimal treatment initiation timing for enhanced chemotherapy outcomes.

NatureVol. 637(8044)
Utrecht University (NL), Leiden University Medical Center (NL), The Netherlands Cancer Institute (NL), University Medical Center Utrecht (NL), VIB-KU Leuven Center for Cancer Biology (BE), Oncode Institute (NL)
Good health and well-being
Openalex Percentile: Top 5%
Cancer Cells and Metastasis
3.67
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