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Directed movement toward, translocation along, penetration into and exit from vascular networks by breast cancer cells in 3D.


ABSTRACT: We developed a computer-assisted platform using laser scanning confocal microscopy to 3D reconstruct in real-time interactions between metastatic breast cancer cells and human umbilical vein endothelial cells (HUVECs). We demonstrate that MB-231 cancer cells migrate toward HUVEC networks, facilitated by filopodia, migrate along the network surfaces, penetrate into and migrate within the HUVEC networks, exit and continue migrating along network surfaces. The system is highly amenable to 3D reconstruction and computational analyses, and assessments of the effects of potential anti-metastasis monoclonal antibodies and other drugs. We demonstrate that an anti-RHAMM antibody blocks filopodium formation and all of the behaviors that we found take place between MB-231 cells and HUVEC networks.

SUBMITTER: Wessels DJ 

PROVIDER: S-EPMC8331046 | biostudies-literature | 2021 Dec

REPOSITORIES: biostudies-literature

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Directed movement toward, translocation along, penetration into and exit from vascular networks by breast cancer cells in 3D.

Wessels Deborah J DJ   Pujol Claude C   Pradhan Nikash N   Lusche Daniel F DF   Gonzalez Luis L   Kelly Sydney E SE   Martin Elizabeth M EM   Voss Edward R ER   Park Yang-Nim YN   Dailey Michael M   Sugg Sonia L SL   Phadke Sneha S   Bashir Amani A   Soll David R DR  

Cell adhesion & migration 20211201 1


We developed a computer-assisted platform using laser scanning confocal microscopy to 3D reconstruct in real-time interactions between metastatic breast cancer cells and human umbilical vein endothelial cells (HUVECs). We demonstrate that MB-231 cancer cells migrate toward HUVEC networks, facilitated by filopodia, migrate along the network surfaces, penetrate into and migrate within the HUVEC networks, exit and continue migrating along network surfaces. The system is highly amenable to 3D recons  ...[more]

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