Compositions and their uses directed to PTPR alpha
View Patent ↗Disclosed herein are compounds, compositions and methods for modulating the expression of PTPR.alpha. in a cell, tissue or animal. Also provided are methods of target validation. Also provided are uses of disclosed compounds and compositions in the manufacture of a medicament for treatment of diseases and disorders. Also provided are methods for the prevention, amelioration and/or treatment of airway hyperresponsiveness and pulmonary inflammation by administration of antisense compounds targeted to PTPR.alpha.
1. A method for the prevention, amelioration, or treatment of a disease or condition wherein indicators of the disease or condition comprise increased plasma glucose levels, increased plasma lipid levels, increased hepatic triglyceride levels, increased plasma transaminase levels, reduced hepatic function, reduced insulin sensitivity or combinations thereof comprising administering an antisense compound 12 to 35 linked nucleosides in length targeted to a nucleic acid molecule encoding human PTPR alpha to an individual in need of such intervention, wherein plasma glucose levels, plasma lipid levels, hepatic triglyceride levels or plasma transaminase levels are decreased, hepatic function or insulin sensitivity is improved or combinations thereof.
2. The method of claim 1 wherein the disease or condition is fatty liver disease and wherein administration of the compound results in a decrease in plasma lipid levels, a decrease in plasma transaminase levels, a decrease in hepatic triglyceride levels or combinations thereof.
3. The method of claim 1 wherein the disease or condition is type-2 diabetes and wherein administration of the compound results in a decrease in plasma glucose levels, an improvement in insulin sensitivity or combinations thereof.
4. The method of claim 1 wherein the disease or condition is metabolic syndrome and wherein administration of the compound results in a decrease in plasma glucose levels, a decrease in plasma lipid levels, a decrease in hepatic triglyceride levels, an improvement in insulin sensitivity, an improvement in hepatic function, a decrease in plasma transaminase levels or combinations thereof.
5. The method of claim 1 wherein the disease or condition comprises type-2 diabetes, fatty liver, metabolic syndrome or combinations thereof.
6. The method of claim 1 wherein the antisense compound optionally further comprises a complementary strand 15 to 35 nucleobases in length.
7. A method for lowering blood glucose levels in an animal in need thereof by administering an antisense compound 12 to 35 nucleosides in length targeted to a nucleic acid molecule encoding human PTPR alpha.
8. A method for lowering triglyceride levels in an animal in need thereof by administering an antisense compound 12 to 35 nucleosides in length targeted to a nucleic acid molecule encoding human PTPR alpha.
9. The method of claim 8 wherein the triglyceride levels are lowered in the plasma.
10. The method of claim 8 wherein the triglyceride levels are lowered in the liver.
11. The method of claim 7 , 8 , 9 or 10 wherein the animal suffers from type-2 diabetes, fatty liver disease, obesity, metabolic syndrome of combinations thereof.
12. The method of claim 1 , wherein the compound is at least 80% complementary to a target region of the nucleic acid encoding PTPRalpha.
13. The method of claim 1 , wherein the compound optionally includes a complementary strand 15 to 35 nucleobases in length.
14. The method of claim 1 , wherein the compound is an antisense oligonucleotide.
15. The compound of claim 14 , wherein the compound has at least one modified internucleoside linkage, sugar moiety, or nucleobase.
16. The compound of claim 14 , wherein the compound comprises a chimeric oligonucleotide.
17. The compound of claim 15 , wherein the modified internucleoside linkage comprises a phosphorothioate linkage.
18. The compound of claim 15 , wherein the at least one modified sugar moiety comprises a 2′-MOE, a LNA, a 2′-OMe, an ENA, a 2′-F or combinations thereof.
19. The compound of claim 15 , wherein the modified nucleobase comprises 5-methylcytosine.
20. The method of claim 12 , wherein the compound is administered in a pharmaceutical composition comprising the compound and a pharmaceutically acceptable penetration enhancer, carrier, or diluent.