Abstract B18: CXCL10 suppresses tumor angiogenesis and impedes expression of critical angiogenic factors in renal cell carcinoma

Author(s):  
Hyun A Jin ◽  
Jun Hyeok Heo ◽  
You Hyun Kang ◽  
Ki Hong Kim ◽  
Kyung Suk Han ◽  
...  
2019 ◽  
Vol 50 (4) ◽  
pp. 225-233 ◽  
Author(s):  
Shan Xu ◽  
Haibao Zhang ◽  
Yue Chong ◽  
Bing Guan ◽  
Peng Guo

2008 ◽  
Vol 68 (2) ◽  
pp. 545-552 ◽  
Author(s):  
Veronica A. Carroll ◽  
Margaret Ashcroft

2007 ◽  
Vol 100 (1) ◽  
pp. 209-214 ◽  
Author(s):  
Tobias Klatte ◽  
Malte Böhm ◽  
Thomas Nelius ◽  
Stephanie Filleur ◽  
Frank Reiher ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
Alessandro Conti ◽  
Matteo Santoni ◽  
Consuelo Amantini ◽  
Luciano Burattini ◽  
Rossana Berardi ◽  
...  

Vascular endothelial growth factor (VEGF) plays a crucial role in tumor angiogenesis. VEGF expression in metastatic renal cell carcinoma (mRCC) is mostly regulated by hypoxia, predominantly via the hypoxia-induced factor (HIF)/Von Hippel-Lindau (VHL) pathway. Advances in our knowledge of VEGF role in tumor angiogenesis, growth, and progression have permitted development of new approaches for the treatment of mRCC, including several agents targeting VEGF and VEGF receptors: tyrosine kinase pathway, serine/threonine kinases,α5β1-integrin, deacetylase, CD70, mammalian target of rapamycin (mTOR), AKT, and phosphatidylinositol 3′-kinase (PI3K). Starting from sorafenib and sunitinib, several targeted therapies have been approved for mRCC treatment, with a long list of agents in course of evaluation, such as tivozanib, cediranib, and VEGF-Trap. Here we illustrate the main steps of tumor angiogenesis process, defining the pertinent therapeutic targets and the efficacy and toxicity profiles of these new promising agents.


2011 ◽  
Vol 185 (4S) ◽  
Author(s):  
Akio Horiguchi ◽  
Takako Asano ◽  
Kenji Kuroda ◽  
Akinori Sato ◽  
Junichi Asakuma ◽  
...  

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