Oligomeric compounds and compositions for the use in modulation of microRNAs

1. An oligomeric compound comprising an oligonucleotide consisting of 17 to 29 nucleosides linked by internucleoside linking groups, said oligonucleotide having an internal region located between two external regions, wherein each external region independently comprises from 1 to 3 nucleosides, each external region comprises a stabilizing modification, and the internal region comprises at least 10 β-D-2′-deoxy-2′-fluororibofuranosyl nucleosides; and wherein the oligomeric compound comprises a sequence substantially complementary to a microRNA.

2. An oligomeric compound comprising an oligonucleotide having the formula:

5′-T 1 -(Nu 1 -L 1 ) n1 -(Nu 2 -L 2 ) n2 -Nu 2 (L 3 -Nu 3 ) n3 -T 2 -3′

wherein:

each Nu 1 and Nu 3 is, independently, a stabilizing nucleoside;

each Nu 2 is a β-D-2′-deoxy-2′-fluororibofuranosyl nucleoside;

each L 1 , L 2 and L 3 is, independently, an internucleoside linking group;

each T 1 and T 2 is, independently, H, a hydroxyl protecting group, an optionally linked conjugate group or a capping group;

n 1 is from 1 to 3;

n 2 is from about 14 to about 22; and

n 3 is from 1 to 3; and wherein the oligomeric compound comprises a sequence substantially complementary to a microRNA.

3. An oligomeric compound comprising an oligonucleotide having the formula I:

T 1 -(Nu 1 ) n1 -(Nu 2 ) n2 -(Nu 3 ) n3 -(Nu n4 )-(Nu 5 ) n5 -T 2 , wherein:

Nu 1 and Nu 5 are, independently, 2′ modified nucleosides;

Nu 2 and Nu 4 are β-D-2′-deoxy-2′-fluororibofuranosyl nucleosides;

Nu 3 is a 2′-modified nucleoside;

each of n1 and n5 is, independently, from 1 to 3;

the sum of n2 plus n4 is between 10 and 25;

n3 is from 0 and 5;

each T 1 and T 2 is, independently, H, a hydroxyl protecting group, an optionally linked conjugate group or a capping group; and wherein the oligomeric compound has a sequence substantially complementary to a microRNA.

4. The oligomeric compound of claim 3 , wherein:

the sum of n2 and n4 is 16 or 17;

n1 is 2;

n3 is 2 or 3; and

n5 is 2.

5. The oligomeric compound of claim 3 , wherein the formula I is selected from:

formula I: n1=2, n2=19, n3=0, n4=0, n5=2;

formula I: n1=2, n2=2, n3=3, n4=14, n5=2;

formula I: n1=2, n2=5, n3=3, n4=11, n5=2;

formula I: n1=2, n2=8, n3=3, n4=8, n5=2;

formula I: n1=2, n2=11, n3=3, n4=5, n5=2;

formula I: n1=2, n2=14, n3=3, n4=2, n5=2;

formula I: n1=2, n2=9, n3=3, n=7, n5=2,;

formula I: n1=2, n2=10, n3=3, n4=6, n5=2;

formula I: n1=2, n2=12, n3=3, n4=4, n5=2;

formula I: n1=2, n2 =3, n3=3, n4=13, n5=2;

formula I: n1=2, n2=4, n3=3, n4=12, n5=2;

formula I: n1=2, n2=6, n3=3, n4=10, n5=2;

formula I: n1=2, n2=7, n3=3, n4=9, n5=2;

formula I: n1=2, n2=13, n3=3, n4=3, n5=2;

formula I: n1=2, n2=8, n3=6, n4=5, n5=2;

formula I: n1=2, n2=2, n3=2, n4=15, n5=2;

formula I: n1=2, n2=3, n3=2, n4=14, n5=2;

formula I: n1=2, n2=4, n3=2, n4=13, n5=2;

formula I: n1=2, n2=5, n3=2, n4=12, n5=2;

formula I: n1=2, n2=6, n3=2, n4=11, n5=2;

formula I: n1=2, n2=7, n3=2, n4=10, n5=2;

formula I: n1=2, n2=8, n3=2, n4=9, n5=2;

formula I: n1=2, n2=9, n3=2, n4=8, n5=2;

formula I: n1=2, n2=10, n3=2, n4=7, n5=2;

formula I: n1=2, n2=11, n3=2, n4=6, n5=2;

formula I: n1=2, n2=12, n3=2, n4=5, n5=2;

formula I: n1=2, n2=13, n3=2, n4=4, n5=2;

formula I: n5=2, n2=14, n3=2, n4=3, n5=2; or

formula I: n1=2, n2=15, n3=2, n4=2, n5=2.

6. The oligomeric compound of claim 3 wherein each of the 2′-modified nucleosides independently comprises a 2′-substituent group selected from O—C 1 -C 12 alkyl, substituted O—C 1 -C 12 alkyl, O—C 2 -C 12 alkenyl, substituted O—C 2 -C 12 alkenyl, O—C 2 -C 12 alkynyl, substituted O—C 2 -C 12 alkynyl, amino, substituted amino, amide, substituted amide, aralkyl, substituted aralkyl, O-aralkyl, substituted O-aralkyl, N 3 , SH, CN, OCN, CF 3 , OCF 3 , SOCH 3 , —SO 2 CH 3 , heterocycloalkyl, heterocycloalkaryl, aminoalkylamino and polyalkylamino; and

wherein each substituent group is, independently, halogen, C 1 -C 12 alkyl, substituted C 1 -C 12 alkyl, C 2 -C 12 alkenyl, substituted C 2 -C 12 alkenyl, C 2 -C 12 alkynyl, substituted C 2 -C 12 alkynyl, O—C 1 -C 12 alkyl, substituted O—C 1 -C 12 alkyl, S—C 1 -C 12 alkyl, substituted S—C 1 -C 12 alkyl, acyl (C(═O)—H), substituted acyl, amino, substituted amino, amide, substituted amide, C 1 -C 12 alkylamino, substituted C 1 -C 12 alkylamino, C 1 -C 12 aminoalkoxy, substituted C 1 -C 12 aminoalkoxy, C 1 -C 12 alkylaminooxy, substituted C 1 -C 12 alkylaminooxy, guanidinyl, substituted guanidinyl or a protecting group.

7. The oligomeric compound of claim 6 wherein each 2′-substituent group is, independently, OCH 3 or O—(CH 2 ) 2 —OCH 3 .

8. The oligomeric compound of claim 7 wherein each 2′-substituent group is O—(CH 2 ) 2 —OCH 3 .

9. The oligomeric compound of claim 3 , wherein the 2′-modified nucleoside is a bicyclic sugar modified nucleoside.

10. The oligomeric compound of claim 9 wherein each of the bicyclic sugar modified nucleosides independently comprises a bridge group between the 2′ and the 4′-carbon atoms comprising from 1 to 8 linked biradical groups independently selected from —O—, —S—, —N(R 1 )—, —C(R 1 )(R 2 )—, —C(R 1 )═C(R 1 )—, —C(R 1 )═N—, —C(═NR 1 )—, —Si(R 1 )(R 2 )—, —S(═O) 2 —, —S(═O)—, —C(═O)—and —C(═S)—;

each R 1 and R 2 is, independently, H, hydroxyl, C 1 -C 12 alkyl, substituted C 1 -C 12 alkyl, C 2 -C 12 alkenyl, substituted C 2 -C 12 alkenyl, C 2 -C 12 alkynyl, substituted C 2 -C 12 alkynyl, C 5 -C 20 aryl, substituted C 5 -C 20 aryl, a heterocycle radical, a substituted heterocycle radical, heteroaryl, substituted heteroaryl, C 5 -C 7 alicyclic radical, substituted C 5 -C 7 alicyclic radical, halogen, substituted oxy (—O—), amino, substituted amino, azido, carboxyl, substituted carboxyl, acyl, substituted acyl, CN, thiol, substituted thiol, sulfonyl (S(═O) 2 —H), substituted sulfonyl, sulfoxyl (S(═O)—H) or substituted sulfoxyl; and

wherein each substituted group comprises a substituent group, independently selected from among, halogen, C 1 -C 12 alkyl, substituted C 1 -C 12 alkyl, C 2 -C 12 alkenyl, substituted C 2 -C 12 alkenyl, C 2 -C 12 alkynyl, substituted C 2 -C 12 alkynyl, amino, substituted amino, acyl, substituted acyl, C 1 -C 12 aminoalkyl, C 1 -C 12 aminoalkoxy, substituted C 1 -C 12 aminoalkyl, substituted C 1 -C 12 aminoalkoxy and a protecting group.

11. The oligomeric compound of claim 10 wherein each bicyclic sugar modified nucleoside independently comprises from 1 to 4 of the linked biradical groups.

12. The oligomeric compound of claim 10 wherein each bridge group is, independently, —CH 2 —, —(CH 2 ) 2 —, —CH 2 —O—, —(CH 2 ) 2 —O—or —CH 2 —N(R 3 )—O— wherein R 3 is H or C 1 -C 12 alkyl.

13. The oligomeric compound of claim 10 wherein each bridge group is, independently, —CH 2 —O—or —(CH 2 ) 2 —O—.

14. The oligomeric compound of claim 3 , wherein Nu 1 is a 2′-modified nucleoside comprising a 2′—O—(CH 2 ) 2 —OCH 3 , Nu 3 is a 2′-modified nucleoside comprising a 2′-O—(CH 2 ) 2 —OCH 3 , Nu 5 is a 2′-modified nucleoside comprising a 2′—O—(CH 2 ) 2 —OCH 3 , T 1 is H and T 2 is H, and wherein formula I is selected from:

formula I: n1=2, n2=19, n3=0, n4=0, n5=2;

formula I: n1=2, n2=2, n3=3, n4=14, n5=2;

formula I: n1=2, n2=5, n3=3, n4=11, n5=2;

formula I: n1=2, n2=8, n3=3, n4=8, n5=2;

formula I: n1=2, n2=11, n3=3, n4=5, n5=2;

formula I: n1=2, n2=14, n3=3, n4=2, n5=2;

formula I: n1=2, n2=9, n3=3, n4=7, n5=2;

formula I: n1=2, n2=10, n3=3, n4=6, n5=2;

formula I: n1=2, n2=12, n3=3, n4=4, n5=2;

formula I: n1=2, n2=3, n3=3, n4=13, n5=2;

formula I: n1=2, n2=4, n3=3, n4=12, n5=2;

formula I: n1=2, n2=6, n3=3, n4=10, n5=2;

formula I: n1=2, n2=7, n3=3, n4=9, n5=2;

formula I: n1=2, n2=13, n3=3, n4=3, n5=2;

formula I: n1=2, n2=8, n3=6, n4=5, n5=2;

formula I: n1=2, n2=2, n3=2, n4=15, n5=2;

formula I: n1=2, n2=3, n3=2, n4=14, n5=2;

formula I: n1=2, n2=4, n3=2, n4=13, n5=2;

formula I: n1=2, n2=5, n3=2, n4=12, n5=2;

formula I: n1=2, n2=6, n3=2, n4=11, n5=2;

formula I: n1=2, n2=7, n3=2, n4=10, n5=2;

formula I: n1=2, n2=8, n3=2, n4=9, n5=2;

formula I: n1=2, n2=9, n3=2, n4=8, n5=2;

formula I: n1=2, n2=10, n3=2, n4=7, n5=2;

formula I: n1=2, n2=11, n3=2, n4=6, n5=2;

formula I: n1=2, n2=12, n3=2, n4=5, n5=2;

formula I: n1=2, n2=13, n3=2, n4=4, n5=2;

formula I: n5=2, n2=14, n3=2, n4=3, n5=2; or

formula I: n1=2, n2=15, n3=2, n4=2, n5=2.

15. The oligomeric compound of any of claim 3 , 5 , or 14 wherein the oligomeric compound comprises at least one phosphorothioate internucleoside linkage.

16. The oligomeric compound of any of claim 3 , 5 , or 14 wherein each internucleoside linkage comprises a phosphorothioate internucleoside linkage.

17. The oligomeric compound of claim 3 wherein T1 is H and T2 is H.

18. The oligomeric compound of claim 3 comprising a sequence selected from SEQ ID NOs 1 to 470.

19. A method of inhibiting miRNA activity, comprising contacting a cell with an oligomeric compound of claim 3 .

20. A method of inhibiting miRNA activity, comprising contacting a cell with an oligomeric compound of claim 1 , wherein the oligomeric compound comprises a sequence selected from SEQ ID NOs 1 to 470.

21. A method of inhibiting miRNA activity, comprising contacting a cell with an oligomeric compound of claim 2 , wherein the oligomeric compound comprises a sequence selected from SEQ ID NOs 1 to 470.

22. A method of inhibiting miRNA activity, comprising contacting a cell with an oligomeric compound of claim 3 , wherein the oligomeric compound comprises a sequence selected from SEQ ID NOs 1 to 470.

23. The method of claim 22 wherein the cell is in vitro.

24. The method of claim 22 wherein the cell is in vivo.

25. A method of inhibiting miRNA activity in vivo, comprising contacting an animal with the oligomeric compound of claim 1 , 2 , or 3 , wherein the oligomeric compound comprises a sequence selected from SEQ ID NOs 1 to 470, thereby inhibiting miRNA activity.

26. A method of inhibiting miR-122 activity, comprising contacting an animal with the oligomeric compound of claim 14 , wherein the oligomeric compound comprises the nucleobase sequence of SEQ ID NO: 19.

27. The method of claim 26 , further comprising decreasing cholesterol levels.