Department of Cancer Biology, Metastasis Research Center, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Department of Internal Medicine, Baylor College of Medicine, Houston, TX, USA.
Nat Cancer. 2024 Sep;5(9):1371-1389. doi: 10.1038/s43018-024-00813-1. Epub 2024 Sep 17.
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.
癌与特定器官的转移相关,而对其他器官则具有选择性。乳腺癌常发生肺转移,但很少发生肾转移。以这种差异为例,我们探究了器官特异性转移倾向背后的机制。我们使用自发和植入的转移性乳腺肿瘤模型,结合炎症组织纤维化、单细胞测序分析和功能研究,揭示了器官特异性转移的因果决定因素。在这里,我们表明,血管生成素 2(Ang2)介导的肺特异性内皮紧密连接蛋白 Claudin 5 的抑制促进了肺转移,而炎症性纤维微环境则增强了这种抑制作用,抗 Ang2 阻断抗体则可以阻止这种抑制作用,而肾转移则被非 Ang2 反应性 Claudin 2 和 10 所阻止。 Claudin 2 和 10 的抑制足以诱导肾转移的出现。这项研究说明了器官特异性血管异质性在决定器官趋向性转移中的影响,而这种影响独立于癌细胞内在机制。