US2013236889A1PendingUtilityA1

Vascularization Inhibitors

49
Assignee: KISHIMOTO TADAMITSUPriority: Mar 24, 1998Filed: Aug 8, 2011Published: Sep 12, 2013
Est. expiryMar 24, 2018(expired)· nominal 20-yr term from priority
G01N 33/5011A61P 43/00A61P 35/00A61K 38/1793
49
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Claims

Abstract

This invention provides a therapeutic agent for inhibiting neovascularization, a therapeutic agent for a solid cancer, a therapeutic agent for a disease pathologically caused by neovascularization, and a therapeutic agent for repairing a tissue comprising as the effective ingredient, a substance that potentiates the action of CXCR4. Based on the finding that vascularization is suppressed in CXCR4 knockout mice, it becomes possible to prepare a therapeutic agent for suppressing vascularization, a therapeutic agent for a solid cancer, a therapeutic agent for a disease pathologically caused by neovascularization, each of which comprises as the effective ingredient, a substance that inhibits the action of CXCR4, as well as to prepare a therapeutic agent for repairing a tissue comprising as the effective ingredient, a substance that potentiates the action of CXCR4. Methods for treatment are made possible that use these therapeutic agents.

Claims

exact text as granted — not AI-modified
1 - 27 . (canceled) 
     
     
         28 . A method for screening a substance that inhibits vascularization, treats a solid cancer or treats a disease pathologically caused by neovascularization, based on the inhibition of the action due to CXCR4, which comprises a step of identifying a substance that inhibits the action due to CXCR4 as a substance that inhibits vascularization, treats a solid cancer or treats a disease pathologically caused by neovascularization. 
     
     
         29 . The method according to  claim 28 , which comprises a step of identifying a substance that inhibits (1) the binding between SDF-1 and CXCR4, (2) the signaling from CXCR4 to nuclei, (3) the expression of CXCR4, or (4) the expression of SDF-1 as a substance that inhibits vascularization, treats a solid cancer or treats a disease pathologically caused by neovascularization. 
     
     
         30 . A method for evaluating vascularization inhibitory activity, anti-solid tumor activity or anti-disease pathologically caused by neovascularization activity of a substance, based on the inhibition of the action due to CXCR4, which comprises a step of measuring the inhibitory activity of the action due to CXCR4. 
     
     
         31 . The method according to  claim 30 , which comprises a step of measuring the inhibitory activity of (1) the binding between SDF-1 and CXCR4, (2) the signaling from CXCR4 to nuclei, (3) the expression of CXCR4, or (4) the expression of SDF-1.

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