US2011177075A1PendingUtilityA1

Targeting pax2 for the induction of defb1-mediated tumor immunity and cancer therapy

Assignee: UNIV SOUTH CAROLINAPriority: Oct 14, 2005Filed: Jan 19, 2011Published: Jul 21, 2011
Est. expiryOct 14, 2025(expired)· nominal 20-yr term from priority
C12N 15/115C12N 15/113A61P 35/00C12N 2310/111C12N 2310/14A61P 35/04C07K 14/4723
59
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Claims

Abstract

Provided is a method of treating cancer in a subject by inhibiting expression of PAX2. An example of a cancer treated by the present method is prostate cancer. In the cancer treatment methods disclosed, the method of inhibiting expression of PAX2 can be by administration of a nucleic acid encoding an siRNA for PAX2. A method of treating cancer in a subject by administering DEFB1 is also provided. Similarly, provided is a method of treating cancer in a subject by increasing expression of DEFB1 in the subject.

Claims

exact text as granted — not AI-modified
1 - 11 . (canceled) 
     
     
         12 . A method for treating cancer in a subject, comprising:
 administering an effective amount of an anti-PAX2 agent to said subject,   wherein said anti-PAX2 agent comprises an anti-PAX2 antibody.   
     
     
         13 . The method of  claim 12 , wherein said cancer is prostate cancer. 
     
     
         14 . The method of  claim 12 , wherein said anti-PAX2 agent is administered with a pharmaceutically acceptable carrier. 
     
     
         15 . The method of  claim 12 , wherein said anti-PAX2 agent is administered parenterally. 
     
     
         16 . The method of  claim 12 , wherein said anti-PAX2 agent is administered subcutaneously. 
     
     
         17 . The method of  claim 12 , wherein said anti-PAX2 agent is administered intramuscularly. 
     
     
         18 . The method of  claim 12 , wherein said anti-PAX2 agent is administered intravenously. 
     
     
         19 . The method of  claim 12 , wherein said anti-PAX2 agent is formulated for sustained release. 
     
     
         20 . The method of  claim 12 , wherein said anti-PAX2 agent is conjugated to an antibody to target a particular cell type. 
     
     
         21 . The method of  claim 12 , wherein said anti-PAX2 agent is conjugated to a receptor to target a particular cell type. 
     
     
         22 . The method of  claim 12 , wherein said anti-PAX2 agent is conjugated to a receptor ligand to target a particular cell type. 
     
     
         23 . A composition for treating cancer, comprising:
 an effective amount of an anti-PAX2 antibody; and   a pharmaceutically acceptable carrier,   wherein said composition is formulated for parenteral administration.   
     
     
         24 . The composition of  claim 23 , wherein said composition is formulated for intramuscular administration. 
     
     
         25 . The composition of  claim 23 , wherein said composition is formulated for intravenous administration. 
     
     
         26 . The composition of  claim 23 , wherein said composition is formulated for subcutaneous administration. 
     
     
         27 . The composition of  claim 23 , wherein said composition is formulated for sustained release. 
     
     
         28 . The composition of  claim 23 , wherein said anti-PAX2 agent is conjugated to an antibody to target a particular cell type. 
     
     
         29 . The composition of  claim 23 , wherein said anti-PAX2 agent is conjugated to a receptor to target a particular cell type. 
     
     
         30 . The composition of  claim 23 , wherein said anti-PAX2 agent is conjugated to a receptor ligand to target a particular cell type. 
     
     
         31 . The composition of  claim 23 , wherein said pharmaceutically acceptable carrier comprises semipermeable matrices of solid hydrophobic polymers and wherein said matrices are in the form of shaped articles.

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