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Effect of Nitroxoline on Angiogenesis and Growth of Human Bladder Cancer
- Source :
- JNCI: Journal of the National Cancer Institute. 102:1855-1873
- Publication Year :
- 2010
- Publisher :
- Oxford University Press (OUP), 2010.
-
Abstract
- Angiogenesis plays an important role in tumor growth and metastasis; therefore, inhibition of angiogenesis is a promising strategy for developing new anticancer drugs. Type 2 methionine aminopeptidase (MetAP2) protein is likely a molecular target of angiogenesis inhibitors.Nitroxoline, an antibiotic used to treat urinary tract infections, was identified from a high-throughput screen of a library of 175,000 compounds for MetAP2 inhibitors and from a parallel screen using the Johns Hopkins Drug Library to identify currently used clinical drugs that can also inhibit human umbilical vein endothelial cells (HUVEC) proliferation. To investigate the mechanism of action of nitroxoline, inhibition of MetAP2 activity and induction of senescence were assessed in HUVEC. To test the antiangiogenic activity of nitroxoline, endothelial tube formation in Matrigel and microvessel formation in Matrigel plugs in vivo were assessed. Antitumor efficacy of nitroxoline was evaluated in mouse models of human breast cancer xenograft (n = 10) and bladder cancer orthotopic xenograft (n = 11). Furthermore, the mechanism of action of nitroxoline was investigated in vivo.Nitroxoline inhibited MetAP2 activity in vitro (half maximal inhibitory concentration [IC(50)] = 54.8 nM, 95% confidence interval [CI] = 22.6 to 132.8 nM) and HUVEC proliferation (IC(50) = 1.9 μM, 95% CI = 1.54 to 2.39 μM). Nitroxoline inhibited MetAP2 activity in HUVEC in a dose-dependent manner and induced premature senescence in a biphasic manner. Nitroxoline inhibited endothelial tube formation in Matrigel and reduced microvessel density in vivo. Mice (five per group) treated with nitroxoline showed a 60% reduction in tumor volume in breast cancer xenografts (tumor volume on day 30, vehicle vs nitroxoline, mean = 215.4 vs 86.5 mm(3), difference = 128.9 mm(3), 95% CI = 32.9 to 225.0 mm(3), P = .012) and statistically significantly inhibited growth of bladder cancer in an orthotopic mouse model (tumor bioluminescence intensities of vehicle [n = 5] vs nitroxoline [n = 6], P = .045).Nitroxoline shows promise as a potential therapeutic antiangiogenic agent.
- Subjects :
- Umbilical Veins
Cancer Research
Angiogenesis
Angiogenesis Inhibitors
Aminopeptidases
Metastasis
Mice
chemistry.chemical_compound
Sirtuin 1
Methionyl Aminopeptidases
RNA, Small Interfering
Neovascularization, Pathologic
biology
Reverse Transcriptase Polymerase Chain Reaction
Nitroquinolines
Acetylation
Drug Synergism
Articles
Immunohistochemistry
Recombinant Proteins
Drug Combinations
Oncology
Female
Proteoglycans
Collagen
Sesquiterpenes
Immunoblotting
Anti-Infective Agents, Urinary
Mice, Nude
Breast Neoplasms
Transfection
Cyclohexanes
medicine
Animals
Humans
Cell Proliferation
Glycoproteins
O-(Chloroacetylcarbamoyl)fumagillol
Bladder cancer
Cell growth
Endothelial Cells
Cancer
medicine.disease
Xenograft Model Antitumor Assays
METAP2
Disease Models, Animal
Urinary Bladder Neoplasms
Nitroxoline
chemistry
Immunology
biology.protein
Cancer research
Endothelium, Vascular
Laminin
Subjects
Details
- ISSN :
- 14602105 and 00278874
- Volume :
- 102
- Database :
- OpenAIRE
- Journal :
- JNCI: Journal of the National Cancer Institute
- Accession number :
- edsair.doi.dedup.....a64f2ef32d55451a605cfbce18149856
- Full Text :
- https://doi.org/10.1093/jnci/djq457