Rank signaling drives basal cell-lineage infidelity leading to mammary tumorigenesis

Rank signaling regulates mammary gland development and epithelial differentiation. While Rank is expressed in both basal and luminal cells, its basal-specific role is unclear. Here, using inducible basal-specific Rank expression and lineage tracing, we show that Rank signaling regulates basal cell identity in postnatal mammary glands. Increased basal Rank activity disrupts basal and luminal identities, causing aberrant luminal-like differentiation, lactation defects, and premalignant lesions composed of hybrid basal-derived cells that progress to basal and luminal adenocarcinomas. Conversely, Rank loss reduces tumor formation and also impairs cell identity. Mechanistically, proteomic, transcriptomic, and chromatin analyses reveal that Rank activation drives epigenetic remodeling, leading to basal identity loss and tumor initiation. A basal Rank gene signature correlates with ductal carcinoma in situ recurrence, as well as poor outcomes in luminal breast cancers. Thus, basal Rank-driven lineage infidelity promotes pre-invasive lesions and transition to invasive breast cancer in females.

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Publication Details

Journal
Nature Communications
Published
2026-02-27
DOI
https://doi.org/10.1038/s41467-026-70020-2
Primary Topic
Hedgehog Signaling Pathway Studies
Type
article
Field-Weighted Citation Impact
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article

Rank signaling drives basal cell-lineage infidelity leading to mammary tumorigenesis

Helga Bergholtz, Pilar Ximénez‐Embún, Eva González‐Suárez, Felipe Cortés‐Ledesma et al.
Nature Communications
Hedgehog Signaling Pathway Studies
article

Rank signaling drives basal cell-lineage infidelity leading to mammary tumorigenesis

Helga Bergholtz, Pilar Ximénez‐Embún, Eva González‐Suárez, Felipe Cortés‐Ledesma, Osvaldo Graña‐Castro, Jaime Redondo-Pedraza, Christopher G. Mueller, Gonzalo Soria-Alcaide, Walid Khaled, Therese Sørlie, Eduardo Caleiras, Marta Isasa, Patricia G. Santamaría, Víctor López, Heena Dalal, Alejandro Sanchez-Juan, José Terrón-Bautista, María Jimenez, G. Kenneth Gray, Ruth Álvarez, Ana Sofia Rocha
article en

Abstract

Rank signaling regulates mammary gland development and epithelial differentiation. While Rank is expressed in both basal and luminal cells, its basal-specific role is unclear. Here, using inducible basal-specific Rank expression and lineage tracing, we show that Rank signaling regulates basal cell identity in postnatal mammary glands. Increased basal Rank activity disrupts basal and luminal identities, causing aberrant luminal-like differentiation, lactation defects, and premalignant lesions composed of hybrid basal-derived cells that progress to basal and luminal adenocarcinomas. Conversely, Rank loss reduces tumor formation and also impairs cell identity. Mechanistically, proteomic, transcriptomic, and chromatin analyses reveal that Rank activation drives epigenetic remodeling, leading to basal identity loss and tumor initiation. A basal Rank gene signature correlates with ductal carcinoma in situ recurrence, as well as poor outcomes in luminal breast cancers. Thus, basal Rank-driven lineage infidelity promotes pre-invasive lesions and transition to invasive breast cancer in females.

Nature Communications
Universidad San Pablo CEU (ES), Oslo University Hospital (NO), Centre National de la Recherche Scientifique (FR), Harvard University (US), University of Cambridge (GB), Institut d'Investigació Biomédica de Bellvitge (ES), Spanish National Cancer Research Centre (ES), Immunologie, Immunopathologie et Chimie Thérapeutique (FR), Centro de Investigación del Cáncer (ES)
Gender equality
Openalex Percentile: Top 40%
Hedgehog Signaling Pathway Studies
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