KRAS nucleic acids and uses thereof
Disclosed herein are molecules and pharmaceutical compositions that mediate RNA interference against KRAS. Also described herein include methods for treating a disease or disorder that comprises a molecule or a pharmaceutical composition that mediate RNA interference against KRAS.
1. A polynucleic acid molecule that mediates RNA interference against Kirsten Rat Sarcoma Viral Oncogene Homolog (KRAS), comprising a sense strand and an antisense strand that hybridizes to a KRAS target sequence selected from SEQ ID NOs: 3, 4, 9, and 15, wherein:
the polynucleic acid molecule comprises 100% modification of nucleotides, wherein the sense strand comprises nnN′nN′n at the 5′ end, and the antisense strand comprises N′N′nN′nN′ at the 5′ end, and wherein n is 2′-O′-methyl modified nucleotide and N′ is 2′-F modified nucleotide; and
the sense strand and the antisense strand are each at least 19, 20, 21, 22, 23, 24, or 25 nucleotides in length.
2. The polynucleic acid molecule of claim 1 , wherein the 2′ O-Me modified nucleotide comprises locked nucleic acid (LNA) or ethylene nucleic acid (ENA).
3. The polynucleic acid molecule of claim 1 , further comprising at least one inverted abasic moiety at at least one terminus.
4. The polynucleic acid molecule of claim 1 , wherein the sense strand and the antisense strand are each 19, 20, or 21 nucleotides in length.
5. The polynucleic acid molecule of claim 1 , wherein the sense strand or the antisense strand comprises at least 45% 2′-O-methyl modification.
6. The polynucleic acid molecule of claim 1 , wherein the sense strand and the antisense strand each independently comprises RNA molecules.
7. The polynucleic acid molecule of claim 1 , wherein the sense strand comprises a sequence having at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or 100% sequence identity to a sequence selected from SEQ ID NOs: 20-23, 32, 33, 44, 45, 50-53, 62, 63, 74, and 75.
8. The polynucleic acid molecule of claim 1 , wherein the antisense strand comprises a sequence having at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or 100% sequence identity to a sequence selected from SEQ ID NOs: 20-23, 32, 33, 44, 45, 50-53, 62, 63, 74, and 75.
9. The polynucleic acid molecule of claim 1 , wherein the polynucleic acid molecule comprises two contiguous modified T or U residues at the 3′ terminus.
10. The polynucleic acid molecule of claim 1 , wherein the polynucleic acid molecule comprises at least one inverted abasic moiety.
11. The polynucleic acid molecule of claim 1 , wherein the sense strand comprises at least one inverted abasic moiety.
12. The polynucleic acid molecule of claim 11 , wherein the at least one inverted abasic moiety is at the 5′ terminus of the sense strand.
13. The polynucleic acid molecule of claim 11 , wherein the at least one inverted abasic moiety is at the 3′ terminus of the sense strand.
14. A pharmaceutical composition comprising:
a) a molecule of claim 1 ; and
b) a pharmaceutically acceptable excipient.
15. The pharmaceutical composition of claim 14 , wherein the pharmaceutical composition is formulated as a nanoparticle formulation.
16. The pharmaceutical composition of claim 14 , wherein the pharmaceutical composition is formulated for parenteral, oral, intranasal, buccal, rectal, or transdermal administration.
17. A polynucleic acid molecule that mediates RNA interference against Kirsten Rat Sarcoma Viral Oncogene Homolog (KRAS), comprising a sense strand and an antisense strand that hybridizes to a KRAS target sequence selected from SEQ ID NOs: 3, 4, 9, and 15, wherein:
the polynucleic acid molecule comprises 100% modification of nucleotides, wherein the sense strand comprises nnN′nN′n at the 5′ end, and the antisense strand comprises N′N′nN′nN′ at the 5′ end, and wherein n is 2′-O′-methyl modified nucleotide and N′ is 2′-F modified nucleotide;
the sense strand comprises an inverted abasic moiety at the 3′ terminus and the 5′ terminus of the sense strand; and
the polynucleic acid molecule comprises at least one phosphorodithioate linkages at the 3′ terminus of the sense strand and the antisense strand.