US2005227938A1PendingUtilityA1

Antisense modulation of TFAP2C expression

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Assignee: BENNETT C FPriority: Jun 26, 1998Filed: Dec 17, 2004Published: Oct 13, 2005
Est. expiryJun 26, 2018(expired)· nominal 20-yr term from priority
C12N 15/1138A61K 38/00C12N 2310/315C12N 2310/321C12N 2310/322C12N 2310/335C12N 2310/341C12N 2310/346Y02P20/582
61
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Claims

Abstract

Antisense compounds, compositions and methods are provided for modulating the expression of TFAP2C. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding TFAP2C. Methods of using these compounds for modulation of TFAP2C expression and for treatment of diseases associated with expression of TFAP2C are provided.

Claims

exact text as granted — not AI-modified
1 . A compound 8 to 50 nucleobases in length targeted to a nucleic acid molecule encoding TFAP2C, wherein said compound specifically hybridizes with said nucleic acid molecule encoding TFAP2C and inhibits the expression of TFAP2C.  
     
     
         2 . The compound of  claim 1  which is an antisense oligonucleotide.  
     
     
         3 . The compound of  claim 2  wherein the antisense oligonucleotide has a sequence comprising SEQ ID NO: 18, 20, 23, 24, 31, 33, 36, 37, 38, 39, 44, 45, 46, 47, 48, 50, 51, 52, 53, 54, 56, 57, 58, 59, 60, 62, 63, 65, 66, 71, 75, 77, 78, 80, 82, 83, 84 or 85.  
     
     
         4 . The compound of  claim 2  wherein the antisense oligonucleotide comprises at least one modified internucleoside linkage.  
     
     
         5 . The compound of  claim 4  wherein the modified internucleoside linkage is a phosphorothioate linkage.  
     
     
         6 . The compound of  claim 2  wherein the antisense oligonucleotide comprises at least one modified sugar moiety.  
     
     
         7 . The compound of  claim 6  wherein the modified sugar moiety is a 2′-O-methoxyethyl sugar moiety.  
     
     
         8 . The compound of  claim 2  wherein the antisense oligonucleotide comprises at least one modified nucleobase.  
     
     
         9 . The compound of  claim 8  wherein the modified nucleobase is a 5-methylcytosine.  
     
     
         10 . The compound of  claim 2  wherein the antisense oligonucleotide is a chimeric oligonucleotide.  
     
     
         11 . A compound 8 to 50 nucleobases in length which specifically hybridizes with at least an 8-nucleobase portion of an active site on a nucleic acid molecule encoding TFAP2C.  
     
     
         12 . A composition comprising the compound of  claim 1  and a pharmaceutically acceptable carrier or diluent.  
     
     
         13 . The composition of  claim 12  further comprising a colloidal dispersion system.  
     
     
         14 . The composition of  claim 12  wherein the compound is an antisense oligonucleotide.  
     
     
         15 . A method of inhibiting the expression of TFAP2C in cells or tissues comprising contacting said cells or tissues with the compound of  claim 1  so that expression of TFAP2C is inhibited.  
     
     
         16 . A method of treating an animal having a disease or condition associated with TFAP2C comprising administering to said animal a therapeutically or prophylactically effective amount of the compound of  claim 1  so that expression of TFAP2C is inhibited.  
     
     
         17 . The method of  claim 16  wherein the disease or condition is a hyperproliferative disorder.  
     
     
         18 . The method of  claim 17  wherein the hyperproliferative disorder is cancer.  
     
     
         19 . The method of  claim 18  wherein the cancer is selected from the group consisting of breast cancer and colon cancer.  
     
     
         20 . The method of  claim 16  wherein the disease or condition is a developmental disorder.

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