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CS2164, a novel multi-target inhibitor against tumor angiogenesis, mitosis and chronic inflammation with anti-tumor potency.
- Source :
-
Cancer science [Cancer Sci] 2017 Mar; Vol. 108 (3), pp. 469-477. Date of Electronic Publication: 2017 Mar 07. - Publication Year :
- 2017
-
Abstract
- Although inhibitors targeting tumor angiogenic pathway have provided improvement for clinical treatment in patients with various solid tumors, the still very limited anti-cancer efficacy and acquired drug resistance demand new agents that may offer better clinical benefits. In the effort to find a small molecule potentially targeting several key pathways for tumor development, we designed, discovered and evaluated a novel multi-kinase inhibitor, CS2164. CS2164 inhibited the angiogenesis-related kinases (VEGFR2, VEGFR1, VEGFR3, PDGFRα and c-Kit), mitosis-related kinase Aurora B and chronic inflammation-related kinase CSF-1R in a high potency manner with the IC <subscript>50</subscript> at a single-digit nanomolar range. Consequently, CS2164 displayed anti-angiogenic activities through suppression of VEGFR/PDGFR phosphorylation, inhibition of ligand-dependent cell proliferation and capillary tube formation, and prevention of vasculature formation in tumor tissues. CS2164 also showed induction of G2/M cell cycle arrest and suppression of cell proliferation in tumor tissues through the inhibition of Aurora B-mediated H3 phosphorylation. Furthermore, CS2164 demonstrated the inhibitory effect on CSF-1R phosphorylation that led to the suppression of ligand-stimulated monocyte-to-macrophage differentiation and reduced CSF-1R <superscript>+</superscript> cells in tumor tissues. The in vivo animal efficacy studies revealed that CS2164 induced remarkable regression or complete inhibition of tumor growth at well-tolerated oral doses in several human tumor xenograft models. Collectively, these results indicate that CS2164 is a highly selective multi-kinase inhibitor with potent anti-tumor activities against tumor angiogenesis, mitosis and chronic inflammation, which may provide the rationale for further clinical assessment of CS2164 as a therapeutic agent in the treatment of cancer.<br /> (© 2016 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.)
- Subjects :
- 3T3 Cells
Animals
Aurora Kinase B antagonists & inhibitors
Cell Line, Tumor
Cell Proliferation drug effects
Female
Histones metabolism
Humans
Inflammation drug therapy
Mice
Mice, Inbred BALB C
Mice, Nude
Molecular Docking Simulation
Naphthalenes
Phosphorylation drug effects
Proto-Oncogene Proteins c-kit antagonists & inhibitors
Receptor, Platelet-Derived Growth Factor alpha antagonists & inhibitors
Receptors, Granulocyte-Macrophage Colony-Stimulating Factor antagonists & inhibitors
Receptors, Vascular Endothelial Growth Factor antagonists & inhibitors
Xenograft Model Antitumor Assays
Adenocarcinoma drug therapy
Angiogenesis Inhibitors therapeutic use
Colonic Neoplasms drug therapy
M Phase Cell Cycle Checkpoints drug effects
Mitosis drug effects
Neovascularization, Pathologic drug therapy
Phenylenediamines therapeutic use
Quinolines therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 1349-7006
- Volume :
- 108
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Cancer science
- Publication Type :
- Academic Journal
- Accession number :
- 28004478
- Full Text :
- https://doi.org/10.1111/cas.13141