Compounds and compositions including phosphorothioated oligodeoxynucleotide, and methods of use thereof
The present disclosure relates to a compound including a nucleic acid sequence conjugated to an anti-microRNA or a microRNA-mimic or a compound including a modified anti-microRNA sequence, compositions of such a compound, and method of treatment of a disease, and method of suppressing microRNA activity by the disclosed compound or composition.
1. A pharmaceutical composition comprising a pharmaceutically acceptable excipient, a compound comprising a phosphorothioated CpG oligodeoxynucleotide (CpG-ODN) conjugated to an anti-miR126 nucleic acid, and an anti-tumor or anti-cancer agent.
2. The pharmaceutical composition compound of claim 1 , further comprising a covalent linker between the CpG-ODN and anti-miR126 nucleic acid.
3. The pharmaceutical composition of claim 2 , wherein the linker is a substituted or unsubstituted alkylene, substituted or unsubstituted heteroalkylene, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkylene, substituted or unsubstituted arylene, or substituted or unsubstituted heteroarylene.
4. The pharmaceutical composition of claim 2 , wherein the linker is a substituted or unsubstituted C 1 -C 40 alkylene, substituted or unsubstituted 2 to 40 membered heteroalkylene, substituted or unsubstituted C 3 -C 8 cycloalkylene, substituted or unsubstituted 3 to 8 membered heterocycloalkylene, substituted or unsubstituted C 6 -C 10 arylene, or substituted or unsubstituted 5 to 10 membered heteroarylene.
5. The pharmaceutical composition of claim 2 , wherein the linker is an unsubstituted C 1 -C 40 alkylene, unsubstituted 2 to 40 membered heteroalkylene, unsubstituted C 3 -C 8 cycloalkylene, unsubstituted 3 to 8 membered heterocycloalkylene, unsubstituted C 6 -C 10 arylene, or unsubstituted 5 to 10 membered heteroarylene.
6. The pharmaceutical composition of claim 2 , wherein the linker is a substituted 2 to 40 membered heteroalkylene.
7. The pharmaceutical composition of claim 1 , wherein said anti-miR126 nucleic acid is chemically modified.
8. The pharmaceutical composition of claim 7 , wherein said anti-miR126 nucleic acid comprises a chemical modification selected for the group consisting of a 2′ O-Methyl, 2′-deoxy-2′fluoro, 2′-deoxy, a universal base, 5-C-methyl, an inverted deoxy abasic residue incorporation, and a locked nucleic acid.
9. The pharmaceutical composition of claim 8 , wherein said modification is positioned at the terminal nucleobase of said anti-miR126 nucleic acid.
10. The pharmaceutical composition of claim 8 , wherein the modification is not positioned at the terminal nucleobase of said anti-miR126 nucleic acid.
11. The pharmaceutical composition of claim 8 , wherein said modification protects against serum-derived nucleases.
12. The pharmaceutical composition of claim 1 , wherein said CpG-ODN nucleic acid sequence is selected from the group consisting of a Class A CpG-ODN nucleic acid sequence, a Class B CpG-ODN nucleic acid sequence, and a Class C CpG-ODN nucleic acid sequence.
13. The pharmaceutical composition of claim 1 , wherein said CpG-ODN comprises phosphodiester derivative linkage selected from the group consisting of a phosphoramidate linkage, phosphorodiamidate linkage, phosphorodithioate linkage, phosphonocarboxylic acid linkage, phosphonocarboxylate linkage, phosphonoacetic acid linkage, phosphonoformic acid linkage, methyl phosphonate linkage, boron phosphonate linkage, and O-methylphosphoroamidite linkage.
14. The pharmaceutical composition of claim 1 , wherein said anti-cancer agent is a cell death promoting agent.
15. The pharmaceutical composition of claim 1 , wherein said anti-cancer agent is selected from the group consisting of: Nilotinib, Actinomycin D / Dactinomycin, Bleomycin, Daunorubicin, Doxorubicin, Doxorubicin (pegylated liposomal), Epirubicin, Idarubicin, Mitomycin, Mitoxantrone, Etoposide, Docetaxel, Irinotecan, Paclitaxel, Topotecan, Vinblastine, Vincristine, Vinorelbine, Carboplatin, Cisplantin, Oxaliplatin, Alemtuzamab, BCG, Bevacizumab, Cetuximab, Denosumab, Erlotinib, Gefitinib, Imatinib, Interferon, Ipilimumab, Lapatinib, Monomethyl auristatin E (MMEA), Mertansine (DM1), Rituximab, Sunitinib, Sorafenib, Temsirolimus, and Trastuzumab, or any combination(s) thereof.