ZFIN ID: ZDB-PUB-130708-56
The perivascular niche regulates breast tumour dormancy
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., Chen, E.I., Lyden, D., and Bissell, M.J.
Date: 2013
Source: Nat. Cell Biol. 15(7): 807-817 (Journal)
Registered Authors: Evason, Kimberley, Stainier, Didier
Keywords: none
MeSH Terms: Animals; Bone Marrow Neoplasms/blood supply; Bone Marrow Neoplasms/metabolism; Bone Marrow Neoplasms/secondary*; Brain Neoplasms/blood supply (all 33) expand
PubMed: 23728425 Full text @ Nat. Cell Biol.
FIGURES   (current status)

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.