Crossing the endothelial barrier during metastasis
By Nicolas Reymond, Bárbara Borda d'Água, A. Ridley. Nature Reviews. Cancer, 2013
881 citations recorded by the source corpus.
Subfields: Cancer Research, Immunology and Allergy, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/5262c679fac48079e7f9e8560db9edfee25763be
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Citations in the corpus
- Tumor angiogenesis and vascular normalization: alternative therapeutic targets (2017, background): “Hypoxic tumor cells often show a more aggressive phenotype, activating oncogenes and undergoing an ‘‘epithelial to mesenchymal transition’’ (EMT), which heightens their metastatic potential [44].”
- Mathematical Modelling of Molecular Pathways Enabling Tumour Cell Invasion and Migration (2015, background): “stroma, cancer cells can migrate to distant sites by intravasation and extravasation of the vascular system [2].”
- Human 3D vascularized organotypic microfluidic assays to study breast cancer cell extravasation (2014, background): “Tissue Eng Part C Methods 19(9):730–737.”
- EMERGING BIOLOGICAL PRINCIPLES OF METASTASIS (2017, neutral): “A uthor M anuscript A uthor M anuscript A uthor M anuscript A uthor M anuscript angiopoietin-like 4 (ANGPTL4), which enhances the permeability of the lung vasculature, promotes TEM of carcinoma cells, and leads to an increased capacity for metastatic outgrowth (Padua et al., 2008).”
- Metastatic Stem Cells: Sources, Niches, and Vital Pathways (2014, background): “blood platelets (Bos et al., 2009; Chabottaux et al., 2009; Chen et al., 2011a; Gay and Felding-Habermann, 2011; Gocheva et al., 2010; Greenberg et al., 2008; Gupta et al., 2007; Kim et al., 2009; Labelle et al., 2011; Li et al., 2010; Padua et al., 2008; Reymond et al., 2013; Rolny et al., 2011; So”
- Rho GTPase signalling in cell migration (2015, background): “Cancer cells also migrate in and out of blood vessels during metastasis [107].”
- Revisiting the hallmarks of cancer. (2017, neutral): “Factors involved in extravasation inlcude ligand-receptor interactions, chemokines, and circulating non-tumor cells, although our understanding of the process is incomplete [122, 124, 125].”