Blockade of Dll4 inhibits tumour growth by promoting non-productive angiogenesis
By Irene Noguera-Troise, C. Daly, N. Papadopoulos, Sandra Coetzee, P. Boland, N. Gale, H. Lin, G. Yancopoulos, Gavin Thurston. Nature, 2006
1,009 citations recorded by the source corpus.
Subfields: Cancer Research, Cell Biology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/226ed9325b992c8787d3e31f9a8755679d897ae2
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Citations in the corpus
- Exciting New Advances in Neuro-Oncology (2010, background): “59 Finally, tumor cells secrete chemokines that serve to recruit proangiogenic myeloid cells to the tumor.”
- The notch ligands Dll4 and Jagged1 have opposing effects on angiogenesis. (2009, neutral): “, 2007; Siekmann and Lawson, 2007), or in experimental tumors (Li et al., 2007; Noguera-Troise et al., 2006; Ridgway et al., 2006).”
- The Canonical Notch Signaling Pathway: Unfolding the Activation Mechanism (2009, background): “Notch signaling has emerged as a specific therapeutic target for T cell acute lymphoblastic leukemia (Weng et al., 2004) and colon cancer (van Es et al., 2005), as well as a potential target in the effort to curb tumor angiogenesis (Noguera-Troise et al., 2006; Ridgway et al., 2006).”
- Vascularization and Angiogenesis in Tissue Engineering: Beyond Creating Static Networks. (2016, background): “Studies that stimulate vascular maturation and stabilization by contrast result in reduced vascular branching and density, but enhanced vessel diameter and perfusion [80].”
- Targeting the tumour vasculature: insights from physiological angiogenesis (2010, background): “The role of DLL4–Notch signalling during physiological angiogenesis is to limit excessive angiogenesis as a negative feedback mechanism and to promote the formation of a functional, mature vasculatur”
- Tumour-initiating cells: challenges and opportunities for anticancer drug discovery (2009, background): “Recently, antibodies that are selective for the Notch ligand Delta-like 4 ( DLL4 ) were shown to inhibit tumour growth by deregulating angiogenesis without much of the toxicity related to γ-secretase inhibition in animal model”