Modeling Mammary Gland Development and Reproductive Cycles With Organoids

Mammary organoids bridge the gap between reductionist 2D systems and in vivo models by recapitulating bilayered epithelial architecture, branching, hormone responsiveness, and, in advanced platforms, functional readouts of lactation. This review synthesizes organoid models across the reproductive cycle, including branching morphogenesis, pregnancy-induced alveologenesis and milk secretion, and involution; it also surveys emerging directions, including embryonic/pluripotent and cross-species systems, as well as co-culture and organ-on-chip platforms that incorporate stromal, adipose, and immune elements. We outline priorities for building more complex, physiologically faithful ex vivo models that will enable mechanistic dissection of mammary development, yield comparative and translational insights, and create scalable platforms for perturbation and screening, advancing lactation research, breast cancer studies, and women's health in general.

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Publication Details

Journal
Biology of the Cell
Published
2025-12-01
DOI
https://doi.org/10.1111/boc.70048
Primary Topic
Cancer Cells and Metastasis
Type
article
Field-Weighted Citation Impact
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article

Modeling Mammary Gland Development and Reproductive Cycles With Organoids

Aurélie Chiche, Han Li, Lamia Djoual, Laurianne Temime
Biology of the Cell
Cancer Cells and Metastasis
article

Modeling Mammary Gland Development and Reproductive Cycles With Organoids

Aurélie Chiche, Han Li, Lamia Djoual, Laurianne Temime
article en

Abstract

Mammary organoids bridge the gap between reductionist 2D systems and in vivo models by recapitulating bilayered epithelial architecture, branching, hormone responsiveness, and, in advanced platforms, functional readouts of lactation. This review synthesizes organoid models across the reproductive cycle, including branching morphogenesis, pregnancy-induced alveologenesis and milk secretion, and involution; it also surveys emerging directions, including embryonic/pluripotent and cross-species systems, as well as co-culture and organ-on-chip platforms that incorporate stromal, adipose, and immune elements. We outline priorities for building more complex, physiologically faithful ex vivo models that will enable mechanistic dissection of mammary development, yield comparative and translational insights, and create scalable platforms for perturbation and screening, advancing lactation research, breast cancer studies, and women's health in general.

Biology of the CellVol. 117(12)
Centre National de la Recherche Scientifique (FR), Institut Pasteur (FR), Université Paris Cité (FR)
Gender equality
Openalex Percentile: Top 30%
Cancer Cells and Metastasis
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