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Cancer discovery · 2026

Cabergoline Suppresses Postpartum Breast Cancer by Enhancing Mammary Gland Involution in Brca1-Mutant Mice and Is Associated with Reduced Risk in Younger Women.

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García-Sancha Natalia, Corchado-Cobos Roberto, Ghorayeb Ryan, Blanco-Gómez Adrián, Cunillera Oriol, Alonso-López Diego, Støer Nathalie C, Mateo Francesca, Espín Roderic, Nguyen Le Tam Nhan, Marzo-Castillejo Mercè, Gough Chelsey L, Milne Katy, Castillo-Lluva Sonia, De Las Rivas Javier, Pozo Julio, Orfao Alberto, Palomero Luis, Pignatelli Jaime, Sacristan-Horcajada Eva, Valero-Juan Luis Félix, Patino-Alonso Carmen, Perera David, Venkitaraman Ashok R, Mao Jian-Hua, Chang Hang, Jiménez-Navas Alejandro, Pérez-Baena Manuel Jesús, Salvador Nélida, Mendiburu-Eliçabe Marina, Gonzalez-Garcia Patricia, Caleiras Eduardo, Peset Isabel, García-Cenador María Begoña, Garcia-Criado Francisco Javier, Nelson Brad H, Botteri Edoardo, Pujana Miquel Angel, Maxwell Christopher A, Pérez-Losada Jesús

Аннотация

Breast cancer that arises in the postpartum period often carries a poor prognosis and urgently requires chemoprevention strategies, particularly for women at elevated risk. Here, we report that a single post-lactation dose of cabergoline, a dopaminergic agonist that blocks prolactin secretion, delays the onset and reduces the incidence of postpartum mammary cancer in K14-Cre; Brca1F/F, Trp53F/F mice. In these mice, cabergoline treatment remodels the mammary gland by potentiating involution, reducing ductal area and proliferation, and reversing T cell exhaustion, potentially through modulation of ion channel expression. Notably, independent retrospective studies in two large cohorts of European women showed that cabergoline treatment was associated with a lower incidence of postpartum breast cancer, with a meta-analysis indicating an approximate 69% reduction in risk. Our work underscores the importance of targeting postlactational involution as a strategy for the prevention of postpartum breast cancer and positions cabergoline as a novel, low-risk chemoprevention strategy.