US2005049211A1PendingUtilityA1

Antisense modulation of insulin-like growth factor binding protein 5 expression

Priority: Oct 9, 2001Filed: Oct 7, 2002Published: Mar 3, 2005
Est. expiryOct 9, 2021(expired)· nominal 20-yr term from priority
Inventors:Susan M. Freier
C12N 2310/315A61K 38/28C12N 2310/3341C12N 2310/11C12N 15/09C12N 2310/341A61K 38/00C12N 15/113C12N 2310/346C12N 2310/321Y02P20/582
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Claims

Abstract

Antisense compounds, compositions and methods are provided for modulating the expression of insulin-like growth factor binding protein 5. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding insulin-like growth factor binding protein 5. Methods of using these compounds for modulation of insulin-like growth factor binding protein 5 expression and for treatment of diseases associated with expression of insulin-like growth factor binding protein 5 are provided.

Claims

exact text as granted — not AI-modified
1 . A compound 8 to 50 nucleobases in length targeted to the start codon, the coding region, the 3′ untranslated region, an intron or an intron/exon junction of a nucleic acid molecule encoding insulin-like growth factor binding protein 5, wherein said compound specifically hybridizes with said nucleic acid molecule encoding insulin-like growth factor binding protein 5 and inhibits the expression of insulin-like growth factor binding protein 5.  
     
     
         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: 13, 14, 15, 16, 17, 18, 19, 21, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 38, 39, 40, 41, 42 or 43.  
     
     
         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 insulin-like growth factor binding protein 5.  
     
     
         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 insulin-like growth factor binding protein 5 in cells or tissues comprising contacting said cells or tissues with the compound of  claim 1  so that expression of insulin-like growth factor binding protein 5 is inhibited.  
     
     
         16 . A method of treating an animal having a disease or condition associated with insulin-like growth factor binding protein 5 comprising administering to said animal a therapeutically or prophylactically effective amount of the compound of  claim 1  so that expression of insulin-like growth factor binding protein 5 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 of the breast, prostate, pancreas, or neuroendocrine system.  
     
     
         20 . The method of  claim 16  wherein the disease or condition is an inflammatory, developmental or metabolic disorder.

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