Cited by 1,148Cancer Cells and MetastasisAngiogenesis and VEGF in CancerMechanisms of cancer metastasis

The DOI matches its Crossref record; 65 of the 65 references it cites were found in a registry or an index.

The perivascular niche regulates breast tumour dormancy

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Abstract

In a significant fraction of breast cancer patients, distant metastases emerge after years or even decades of latency. How disseminated tumour cells (DTCs) are kept dormant, and what wakes them up, are fundamental problems in tumour biology. To address these questions, we used metastasis assays in mice and showed that dormant DTCs reside on microvasculature of lung, bone marrow and brain. We then engineered organotypic microvascular niches to determine whether endothelial cells directly influence breast cancer cell (BCC) growth. These models demonstrated that endothelial-derived thrombospondin-1 induces sustained BCC quiescence. This suppressive cue was lost in sprouting neovasculature; time-lapse analysis showed that sprouting vessels not only permit, but accelerate BCC outgrowth. We confirmed this surprising result in dormancy models and in zebrafish, and identified active TGF-β1 and periostin as tumour-promoting factors derived from endothelial tip cells. Our work reveals that stable microvasculature constitutes a dormant niche, whereas sprouting neovasculature sparks micrometastatic outgrowth.

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Metadata

Authors
Ghajar, C. M., Peinado, H., Mori, H., Matei, I. R., Evason, K. J., Brazier, H., Almeida, D., Koller, A., Hajjar, K. A., Stainier, D. Y. R., Chen, E. I., Lyden, D., & Bissell, M. J.
Affiliations
  • Lawrence Berkeley National Laboratory (US)
  • Weill Cornell Medicine (US)
  • University of California, San Francisco (US)
  • Stony Brook University (US)
  • Champalimaud Foundation (PT)
Corresponding author
  • Ghajar, Cyrus M.
  • Bissell, Mina J.
Venue
Nature Cell Biology
Published
2013-06-02
Volume
15
Issue
7
Pages
807-817
ISSN
  • 1465-7392 (ISSN-L)
  • 1476-4679
OpenAlex
W2155542819
Cited by
1,148
References
65
Citations by year
2026: 62 · 2025: 68 · 2024: 70 · 2023: 86 · 2022: 89 · 2021: 122 · 2020: 125 · 2019: 97 · 2018: 98 · 2017: 69 · 2016: 89 · 2015: 64 · 2014: 78 · 2013: 29
FWCI
46.44
Type
journal article
Language
en
Open access
Locations
  • Nature Cell Biology (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • Max Planck Institute for Plasma Physics (submittedVersion)
Funders
  • National Heart, Lung, and Blood Institute (R01HL042493, R01HL054737, R01HL090895, HL54737)
  • National Cancer Institute (U54CA126552, U54CA143836, U01CA169538, R37CA064786)
  • National Center for Research Resources (1 S10 RR023680-1, S10RR023680)
Topics
  • Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mechanisms of cancer metastasis
Keywords
breast cancer, tumor dormancy, disseminated tumor cells, perivascular niche, endothelial cells, thrombospondin-1, TGF-β1, periostin, organotypic culture, micrometastases, microcirculation
MeSH terms
Animals, Brain Neoplasms, Breast Neoplasms, Endothelium, Vascular, Female, Fluorescent Antibody Technique, Humans, Lung Neoplasms, Neovascularization, Pathologic, Tumor Cells, Cultured, Zebrafish, Cell Adhesion Molecules, Transforming Growth Factor beta, Neoplasm, Residual, Bone Marrow Neoplasms, Thrombospondin 1, Pericytes, Mice, Stem Cell Niche, Tumor Microenvironment

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