| Literature DB >> 29762071 |
Ana B García-Martín1, Pascale Zwicky1, Thomas Gruber1, Christoph Matti1, Federica Moalli1, Jens V Stein1, David Francisco2, Gaby Enzmann1, Mitchell P Levesque3, Ekkehard Hewer4, Ruth Lyck1.
Abstract
Melanoma is the most aggressive skin cancer in humans. One severe complication is the formation of brain metastasis, which requires extravasation of melanoma cells across the tight blood-brain barrier (BBB). Previously, VLA-4 has been assigned a role for the adhesive interaction of melanoma cells with non-BBB endothelial cells. However, the role of melanoma VLA-4 for breaching the BBB remained unknown. In this study, we used a mouse in vitro BBB model and imaged the shear resistant arrest of melanoma cells on the BBB. Similar to effector T cells, inflammatory conditions of the BBB increased the arrest of melanoma cells followed by a unique post-arrest behavior lacking immediate crawling. However, over time, melanoma cells intercalated into the BBB and compromised its barrier properties. Most importantly, antibody ablation of VLA-4 abrogated melanoma shear resistant arrest on and intercalation into the BBB and protected the BBB from barrier breakdown. A tissue microarray established from human brain metastasis revealed that indeed a majority of 92% of all human melanoma brain metastases stained VLA-4 positive. We propose VLA-4 as a target for the inhibition of brain metastasis formation in the context of personalized medicine identifying metastasizing VLA-4 positive melanoma.Entities:
Keywords: BBB leakage; Blood–brain barrier; in vitro live cell imaging; melanoma brain metastasis; tissue microarray; very late antigen-4
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Year: 2018 PMID: 29762071 PMCID: PMC6775593 DOI: 10.1177/0271678X18775887
Source DB: PubMed Journal: J Cereb Blood Flow Metab ISSN: 0271-678X Impact factor: 6.200