Abstract
Meningiomas are relatively common (22%) vascular brain tumors. 3-11% of meningiomas are malignant, and defy currently available therapy. Inhibition of neovascularization is one potential strategy for treating these hypervascular tumors. Inhibition of tumor-induced angiogenesis by TNP-470 (previously termed AGM-1470), a synthetic analogue of fumagillin, was tested on the growth of human non-malignant and malignant meningiomas in nude mice. TNP-470 significantly inhibited tumor neovascularization and tumor growth of both non-malignant and malignant meningiomas. TNP-470 is now in human trial and should be tested for efficacy in treating malignant or recurrent aggressive meningiomas.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Antibiotics, Antineoplastic / therapeutic use*
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Body Weight / drug effects
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Cell Transplantation
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Cyclohexanes
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Female
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Humans
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Meningeal Neoplasms / blood supply
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Meningeal Neoplasms / drug therapy*
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Meningeal Neoplasms / pathology
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Meningioma / blood supply
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Meningioma / drug therapy*
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Meningioma / pathology
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Mice
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Mice, Inbred BALB C
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Mice, Nude
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Neoplasm Transplantation
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Neovascularization, Pathologic / drug therapy*
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Neovascularization, Pathologic / pathology
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Neurofibromatoses / drug therapy
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O-(Chloroacetylcarbamoyl)fumagillol
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Regional Blood Flow / drug effects
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Sesquiterpenes / therapeutic use*
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Transplantation, Heterologous
Substances
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Antibiotics, Antineoplastic
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Cyclohexanes
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Sesquiterpenes
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O-(Chloroacetylcarbamoyl)fumagillol