Methods and compositions involving miRNA and miRNA inhibitor molecules
View Patent ↗The present invention concerns methods and compositions for introducing miRNA activity or function into cells using synthetic nucleic acid molecules. Moreover, the present invention concerns methods and compositions for identifying miRNAs with specific cellular functions that are relevant to therapeutic, diagnostic, and prognostic applications wherein synthetic miRNAs and/or miRNA inhibitors are used in library screening assays.
1. A method for reducing cell proliferation in a cancer cell comprising providing to the cell an effective amount of a synthetic RNA molecule between 21 and 25 nucleotides in length corresponding to human miR-215, wherein the molecule comprises
a) a first strand having an miRNA region whose sequence from 5′ to 3′ is identical to a mature human miR-215 sequence, and
b) a second separate strand having a complementary region whose sequence from 5′ to 3′ is 100% complementary to the sequence of the miRNA region, wherein the second strand comprises i) at least one chemical modification of the nucleotide at the 5′ end and/or ii) one or more sugar modifications in the first or last 1 to 6 residues.
2. The method of claim 1 , wherein the cancer cell is a breast cancer cell, a cervical cancer cell, a colon cancer cell, or a skin cancer cell.
3. The method of claim 1 , wherein the synthetic RNA molecule is 21 nucleotides in length.
4. The method of claim 1 , wherein the chemical modification of the nucleotide at the 5′ end is biotin, an amine group, a lower alkylamine group, an acetyl group, 2′ oxygen-methyl (2′O-Me), 4,4′-dimethoxytrityl with oxygen (DMTO), fluoroscein, a thiol, or acridine.
5. The method of claim 4 , wherein the chemical modification is a lower alkylamine group.
6. The method of claim 4 , wherein the chemical modification is a 2′OMe.
7. The method of claim 1 , wherein the second strand comprises one or more sugar modifications in the first or last 1 to 6 residues of the complementary strand.
8. The method of claim 7 , wherein the sugar modification is a 2′O-Me modification.
9. The method of claim 7 , comprising one or more sugar modifications in the first 1 to 6 residues of the complementary region.
10. The method of claim 7 , comprising one or more sugar modifications in the last 1 to 6 residues of the complementary strand.
11. The method of claim 1 , wherein the second strand molecule comprises both i) at least one chemical modification of the nucleotide at the 5′ end and ii) one or more sugar modifications in the first or last 1 to 6 residues.
12. The method of claim 10 , wherein i) the chemical modification of the nucleotide at the 5′ end of the second polynucleotide is a lower alkylamine group and ii) there are one or more sugar modifications in the first or last 1 to 6 residues of the second strand.
13. The method of claim 12 , wherein there are one or more sugar modifications in the first and last 1 to 6 residues of the second strand.
14. The method of claim 13 , wherein the modification is a 2′ oxygen-methyl (2′ O-Me).
15. The method of claim 11 , wherein the first and second strands are 100% complementary.
16. The method of claim 10 , wherein the second strand comprises a complementary region whose sequence from 5′ to 3′ is fully complementary to the miRNA sequence, except that there is noncomplementarity between one or more nucleotides in the last 1 to 5 residues at the 3′ end of the complementary region and the corresponding nucleotides of the miRNA region.
17. A method for inhibiting proliferation of a breast cancer cell, a cervical cancer cell, a colon cancer cell, or a skin cancer cell comprising administering to the cell an effective amount of a synthetic RNA molecule 21-26 nucleotides in length comprising:
a) a first polynucleotide comprising an miRNA region whose sequence from 5′ to 3′ is identical to a mature human miR-215 sequence, and
b) a second polynucleotide comprising a complementary region whose sequence from 5′ to 3′ is 100% complementary to the sequence of the miRNA region on the first strand,
wherein, the second polynucleotide comprises i) a lower alkylamine group modification on the 5′ terminal nucleotide and/or ii) one or more sugar modifications in the first or last 1 to 6 residues of the second polynucleotide.
18. The method of claim 17 , wherein the synthetic RNA molecule has two polynucleotides each 21 nucleotides in length.
19. A method for reducing cell viability of lung cancer cells comprising administering to the cells an effective amount of a synthetic RNA molecule comprising:
a) an miRNA region whose sequence from 5′ to 3′ is 90% identical to a mature human miR-215 sequence on a first strand, wherein the sequence is the sequence of a mature human miR-192, and
b) a complementary region whose sequence from 5′ to 3′ is 100% complementary to the sequence of the miRNA region on a second strand,
wherein the molecule comprises two strands of 21-26 nucleotides in length and wherein the 5′ terminus of the second strand further comprises a nucleotide modification.
20. The method of claim 19 , wherein cell viability of lung cancer cells is reduced by inducing apoptosis of the cells.
21. The method of claim 19 , wherein the synthetic RNA molecule has two strands each 21 nucleotides in length.
22. A method for inhibiting proliferation of a breast cancer cell, a cervical cancer cell, a colon cancer cell, or a skin cancer cell comprising providing to the cell a composition comprising a synthetic RNA molecule between 21 and 26 nucleotides in length, wherein the molecule comprises
a) a first strand having an miRNA region whose sequence from 5′ to 3′ is at least 90% identical to a mature human miR-215 sequence, wherein the sequence is a mature human miR-215 sequence or a mature human miR-192 sequence, and
b) a second separate strand having a complementary region whose sequence from 5′ to 3′ is 100% complementary to the sequence of the miRNA region, wherein the second strand comprises i) a modified nucleotide at the 5′ terminus and/or ii) one or more sugar modifications in the first or last 1 to 6 residues of the second strand.
23. The method of claim 22 , wherein the miRNA region has the sequence of a mature human miR-192 sequence.
24. The method of claim 22 , wherein the RNA molecule is 21 nucleotides in length.
25. A method for inhibiting proliferation of a breast cancer cell, a cervical cancer cell, a colon cancer cell, or a skin cancer cell comprising providing to the cell a composition comprising a synthetic RNA molecule between 21 and 26 nucleotides in length, wherein the molecule comprises
a) a first strand having an miRNA region whose sequence from 5′ to 3′ is at least 90% identical to a mature human miR-215 sequence, wherein the sequence is a mature human miR-192 sequence, and
b) a second separate strand having a complementary region whose sequence from 5′ to 3′ is 100% complementary to the sequence of the miRNA region.
26. The method of claim 25 , wherein the separate second strand i) has a modified nucleotide at the 5′ terminus and/or ii) has one or more sugar modifications in the first or last 1 to 6 residues of the second strand.
27. The method of claim 25 , wherein the RNA molecule is 21 nucleotides in length.
28. The method of claim 22 , wherein the cancer cell is a breast cancer cell.
29. The method of claim 22 , wherein the cancer cell is a cervical cancer cell.
30. The method of claim 22 , wherein the cancer cell is a colon cancer cell.
31. The method of claim 22 , wherein the cancer cell is a skin cancer cell.