Directed movement toward, translocation along, penetration into and exit from vascular networks by breast cancer cells in 3D.
Directed movement toward, translocation along, penetration into and exit from vascular networks by breast cancer cells in 3D.
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DOI:
10.1080/19336918.2021.1957527
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发表时间:
2021-12
影响因子:
3.2
通讯作者:
Soll DR
中科院分区:
文献类型:
--
作者:
Wessels DJ;Pujol C;Pradhan N;Lusche DF;Gonzalez L;Kelly SE;Martin EM;Voss ER;Park YN;Dailey M;Sugg SL;Phadke S;Bashir A;Soll DR
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.
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影响因子:
3.2
作者:
Arjonen, Antti;Kaukonen, Riina;Ivaska, Johanna
通讯作者:
Ivaska, Johanna
影响因子:
4.8
作者:
Chen, Chia-Chi;Chen, Li-Li;Huang, Tze-Sing
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影响因子:
15.9
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CHERESH, DA
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Torre V
影响因子:
8.8
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Arwert EN;Harney AS;Entenberg D;Wang Y;Sahai E;Pollard JW;Condeelis JS
通讯作者:
Condeelis JS