US2009023676A1PendingUtilityA1

RNA Interference Mediated Inhibition of MAP Kinase Gene Expression or Expression of Genes Involved in MAP Kinase Pathway Using Short Interfering Nucleic Acid (SiNA)

Assignee: SIRNA THERAPEUTICS INCPriority: Feb 20, 2002Filed: Aug 29, 2008Published: Jan 22, 2009
Est. expiryFeb 20, 2022(expired)· nominal 20-yr term from priority
A61P 37/04A61P 37/06A61P 43/00A61P 37/08A61P 37/00A61P 9/10A61P 41/00A61P 9/00A61P 3/10A61P 5/00A61P 31/00A61P 3/00A61P 27/16A61P 31/10A61P 25/28A61P 31/12A61P 25/16A61P 31/16A61P 29/00A61P 25/02A61P 35/00A61P 35/02A61P 31/18A61P 25/00A61P 25/08A61P 31/04A61P 31/14A61P 27/02A61P 25/14A61P 31/20A61P 31/22C12N 2310/322A61K 47/54A61K 38/00C12N 15/8218A61P 1/16C12N 2310/111A61P 15/00A61P 19/00A61P 11/06C12N 15/1131A61P 13/10A61P 19/02C12N 2310/321C12N 15/1138C12N 2310/317C12N 2310/14C12N 2310/346C07H 21/02A61P 11/00A61P 13/08C12N 2310/344C12N 2310/315A61P 17/02C12N 2310/53A61P 1/00C12N 2320/51A61P 13/12A61P 17/00C12N 2330/30C12N 2310/318C12N 2310/332A61P 21/00A61P 1/04C12N 15/111Y02A50/30
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Claims

Abstract

The present invention concerns methods and reagents useful in modulating MAP kinase gene expression in a variety of applications, including use in therapeutic, diagnostic, target validation, and genomic discovery applications. Specifically, the invention relates to small nucleic acid molecules, such as short interfering nucleic acid (siNA), short interfering RNA (siRNA), double-stranded RNA (dsRNA), micro-RNA (miRNA), and short hairpin RNA (shRNA) molecules capable of mediating RNA interference (RNAi) against c-JUN, JNK, p38, and ERK gene expression, useful in the treatment of cancer, inflammation, obesity and insulin resistance (e.g. Type I and Type II diabetes).

Claims

exact text as granted — not AI-modified
1 . A chemically modified nucleic acid molecule, wherein:
 (a) the nucleic acid molecule comprises a sense strand and a separate antisense strand, each strand having one or more pyrimidine nucleotides and one or more purine nucleotides;   (b) each strand of the nucleic acid molecule is independently 18 to 27 nucleotides in length;   (c) an 18 to 27 nucleotide sequence of the antisense strand is complementary to a human c-Jun RNA sequence comprising SEQ ID NO:1715;   (d) an 18 to 27 nucleotide sequence of the sense strand is complementary to the antisense strand and comprises an 18 to 27 nucleotide sequence of the human RNA sequence; and   (e) 50 percent or more of the nucleotides in at least one strand comprise a 2′-sugar modification, wherein the 2′-sugar modification of any of the pyrimidine nucleotides differs from the 2′-sugar modification of any of the purine nucleotides.   
     
     
         2 . The nucleic acid molecule of  claim 1 , wherein 50 percent or more of the nucleotides in each strand comprise a 2′-sugar modification. 
     
     
         3 . The nucleic acid molecule of  claim 1 , wherein the 2′-sugar modification is selected from the group consisting of 2′-deoxy-2′-fluoro, 2′-O-methyl, and 2′-deoxy. 
     
     
         4 . The nucleic acid of  claim 3 , wherein the 2′-deoxy-2′-fluoro sugar modification is a pyrimidine modification. 
     
     
         5 . The nucleic acid of  claim 3 , wherein the 2′-deoxy sugar modification is a pyrimidine modification. 
     
     
         6 . The nucleic acid of  claim 3 , wherein the 2′-O-methyl sugar modification is a pyrimidine modification. 
     
     
         7 . The nucleic acid molecule of  claim 4 , wherein said pyrimidine modification is in the sense strand, the antisense strand, or both the sense strand and antisense strand. 
     
     
         8 . The nucleic acid molecule of  claim 6 , wherein said pyrimidine modification is in the sense strand, the antisense strand, or both the sense strand and antisense strand. 
     
     
         9 . The nucleic acid molecule of  claim 3 , wherein the 2′-deoxy sugar modification is a purine modification. 
     
     
         10 . The nucleic acid molecule of  claim 3 , wherein the 2′-O-methyl sugar modification is a purine modification. 
     
     
         11 . The nucleic acid molecule of  claim 9 , wherein the purine modification is in the sense strand. 
     
     
         12 . The nucleic acid molecule of  claim 10 , wherein the purine modification is in the antisense strand. 
     
     
         13 . The nucleic acid molecule of  claim 1 , wherein the nucleic acid molecule comprises ribonucleotides. 
     
     
         14 . The nucleic acid molecule of  claim 1 , wherein the sense strand includes a terminal cap moiety at the 5′-end, the 3′-end, or both of the 5′- and 3′-ends. 
     
     
         15 . The nucleic acid molecule of  claim 14 , wherein the terminal cap moiety is an inverted deoxy abasic moiety. 
     
     
         16 . The nucleic acid molecule of  claim 1 , wherein said nucleic acid molecule includes one or more phosphorothioate internucleotide linkages. 
     
     
         17 . The nucleic acid molecule of  claim 16 , wherein one of the phosphorothioate internucleotide linkages is at the 3′-end of the antisense strand. 
     
     
         18 . The nucleic acid molecule of  claim 1 , wherein the 5′-end of the antisense strand includes a terminal phosphate group. 
     
     
         19 . The nucleic acid molecule of  claim 1 , wherein the sense strand, the antisense strand, or both the sense strand and the antisense strand include a 3′-overhang. 
     
     
         20 . A composition comprising the nucleic acid molecule of  claim 1 , in a pharmaceutically acceptable carrier or diluent.

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