Antisense Oligonucleotide (ASO) Gene Inhibition and Treatment
Embodiments of the invention related generally to antisense oligonucleotides (ASOs) and, more particularly, to compositions and methods for regulating protein synthesis using ASOs. In one embodiment, the invention provides a method of treating a patient diagnosed with myelodysplastic syndrome (MDS) comprising: administering to the patient an amount of an antisense oligonucleotide (ASO) targeted to a nucleic acid molecule encoding JAK2 (ASO-T-JAK2) compound effective to treat such disease.
1 . A method of treating a patient diagnosed with myelodysplastic syndrome (MDS) or polycythemia vera (PV) which comprises:
administering to said patient an amount of an ASO-T-JAK2 compound effective to treat such disease, wherein the ASO-T-JAK2 compound is targeted to SEQ ID NO 2, SEQ ID NO 3, or both.
2 . (canceled)
3 . The method of claim 1 , wherein the ASO-T-JAK2 compound comprises a nucleotide sequence including SEQ ID NO 4 or SEQ ID NO 5.
4 . The method of claim 1 , wherein the amount of said ASO-T-JAK2 compound is an amount sufficient to inhibit expression of JAK2 in the patient.
5 - 8 . (canceled)
9 . A method of inhibiting expression of the JAK2 gene in an individual which comprises:
administering to the individual an amount of an ASO-T-JAK2 compound effective to inhibit JAK2 expression in the individual, wherein the ASO-T-JAK2 compound is targeted to SEQ ID NO 2, SEQ ID NO 3, or both.
10 . (canceled)
11 . The method of claim 9 , wherein the ASO-T-JAK2 compound comprises a nucleotide sequence including SEQ ID NO 4 or SEQ ID NO 5.
12 . An antisense oligonucleotide (ASO) targeted to a nucleic acid molecule encoding JAK2, wherein the ASO-T-JAK2 compound is targeted to SEQ ID NO 2, SEQ ID NO 3, or both.
13 . (canceled)
14 . The ASO of claim 12 , wherein the ASO comprises a nucleotide sequence selected from a group consisting of: SEQ ID No 4 and SEQ ID NO 5.
15 . A pharmaceutical composition which comprises:
the ASO of claim 12 ; and
a pharmaceutically acceptable diluent, carrier, adjuvant, or combination thereof.
16 . The composition of claim 15 which further comprises a sterile parenteral dosage form.
17 . A method of treating a patient diagnosed with Charcot-Marie-Tooth type 2 (CMT2) which comprises:
administering to said patient an amount of an ASO-T-IGHMBP2 compound effective to treat such disease.
18 . The method of claim 17 , wherein the patient is diagnosed with Charcot-Marie-Tooth type 2S (CMT2S).
19 . The method of claim 18 , wherein the ASO-T-IGHMBP2 compound is targeted to SEQ ID NO 7.
20 . The method of claim 19 , wherein the ASO-T-IGHMBP2 compound comprises a nucleotide sequence including SEQ ID NO 9.
21 . The method of claim 20 , wherein the ASO-T-IGHMBP2 compound comprises a nucleotide sequence including SEQ ID NO 8.
22 . The method of claim 20 , wherein the ASO-T-IGHMBP2 compound comprises a nucleotide sequence selected from a group consisting of: SEQ ID NO 10, SEQ ID NO 11, and SEQ ID NO 12.
23 . The method of claim 20 , wherein the ASO-T-IGHMBP2 compound comprises a nucleotide sequence 13 to 35 nucleotides in length within SEQ ID NO 15.
24 - 37 . (canceled)