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Vascular heterogeneity of tight junction Claudins guides organotropic metastasis.

Authors :
Zhou X
LeBleu VS
Fletcher-Sananikone E
Kim J
Dai J
Li B
Wu CC
Sugimoto H
Miyake T
Becker LM
Volpert OV
Lawson E
Espinosa Da Silva C
Patel SI
Kizu A
Ehsanipour EA
Sha D
Karam JA
McAndrews KM
Kalluri R
Source :
Nature cancer [Nat Cancer] 2024 Sep; Vol. 5 (9), pp. 1371-1389. Date of Electronic Publication: 2024 Sep 17.
Publication Year :
2024

Abstract

Carcinomas are associated with metastasis to specific organs while sparing others. Breast cancer presents with lung metastasis but rarely kidney metastasis. Using this difference as an example, we queried the mechanism(s) behind the proclivity for organ-specific metastasis. We used spontaneous and implant models of metastatic mammary carcinoma coupled with inflammatory tissue fibrosis, single-cell sequencing analyses and functional studies to unravel the causal determinants of organ-specific metastasis. Here we show that lung metastasis is facilitated by angiopoietin 2 (Ang2)-mediated suppression of lung-specific endothelial tight junction protein Claudin 5, which is augmented by the inflammatory fibrotic microenvironment and prevented by anti-Ang2 blocking antibodies, while kidney metastasis is prevented by non-Ang2-responsive Claudins 2 and 10. Suppression of Claudins 2 and 10 was sufficient to induce the emergence of kidney metastasis. This study illustrates the influence of organ-specific vascular heterogeneity in determining organotropic metastasis, independent of cancer cell-intrinsic mechanisms.<br /> (© 2024. The Author(s), under exclusive licence to Springer Nature America, Inc.)

Details

Language :
English
ISSN :
2662-1347
Volume :
5
Issue :
9
Database :
MEDLINE
Journal :
Nature cancer
Publication Type :
Academic Journal
Accession number :
39289595
Full Text :
https://doi.org/10.1038/s43018-024-00813-1