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February 6, 20260 citationsOpen Access

Niche-labeled single-cell RNA-seq analysis of breast cancer metastatic ecosystems in brain, lung, liver, and bone.

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JIJacob Insua-RodríguezDLDevon A. LawsonKKKai Kessenbrock

Key Points

  • To understand how breast cancer cells colonize different organs and to create a detailed map of metastatic ecosystems.
  • Utilized a mouse model for stage IV breast cancer.
  • Applied niche labeling for targeted identification of metastatic sites.
  • Conducted single-cell RNA sequencing to analyze over 70,000 cells.
  • Generated a comprehensive cellular and molecular atlas of metastasis across brain, lung, liver, and bone.
  • Identified distinct cellular populations in each metastatic niche.
  • Provided insights into the molecular mechanisms of breast cancer metastasis.

Abstract

Metastasis frequently affects multiple organs in stage IV breast cancer patients and is associated with dismal outcomes. The mechanisms enabling cancer cell colonization across diverse anatomical sites remain poorly understood, mainly due to lack of models of systemic disease and of studies in clinical samples involving multiple metastatic sites. Here, we combined metastatic niche labeling with single-cell RNA sequencing (scRNA-seq) in a mouse model of breast cancer multi-organ metastasis, and generated a cellular and molecular atlas of metastatic ecosystems encompassing >70,000 cells across brain, lung, liver, and bone.

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Cite This Study

Insua-Rodríguez et al. (2025) studied this question.

synapsesocial.com/papers/698585db8f7c464f230099eahttps://doi.org/10.5281/zenodo.18326241
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