Method for the modulation of function of transcription factors
There is provided a method of modulating the function of a transcription factor by administering an effective amount of an oligonucleotide containing optimal nucleotide binding site for the transcription factor. A therapeutic agent having an effective amount of an oligonucleotide for modulating function of a transcription factor and a pharmaceutically acceptable carrier is also provided. Also provided is a treatment of patients having illnesses in which the activation of transcription factors plays a role by administering to a patient an effective amount of an oligonucleotide which competitively binds the related transcription factor.
1. A method for treating a person or animal having a disorder associated with the activation of a transcription factor, said method comprising administering to said person or animal an effective amount of a composition comprising a double-stranded oligonucleotide, wherein said transcription factor binds to said oligonucleotide and activation of said transcription factor is thereby inhibited, wherein said oligonucleotide comprises the nucleotide sequence AGATTTCTAGGAATTCAAATC (SEQ ID NO:1).
2. The method according to claim 1 , wherein said transcription factor is a member of the STAT family of transcription factors.
3. The method according to claim 1 , wherein said transcription factor is STAT5.
4. The method according to claim 1 , wherein said transcription factor is activated.
5. The method according to claim 4 , wherein said transcription factor is constitutively activated.
6. The method according to claim 1 , wherein said disorder is a neoplasm.
7. The method according to claim 6 , wherein said neoplasm is a leukemia or carcinoma.
8. The method according to claim 1 , wherein said composition further comprises a pharmaceutically acceptable carrier, diluent, and/or adjuvant.
9. A method of inhibiting the function of a transcription factor in a cell, said method comprising contacting a cell with a double-stranded oligonucleotide. wherein said oligonucleotide is taken into said cell and said transcription factor binds to said oligonucleotide and function of said transcription factor is thereby inhibited, wherein said oligonucleotide comprises the nucleotide sequence AGATTTCTAGGAATTCAAATC (SEQ ID NO:1).
10. The method according to claim 9 , wherein said transcription factor is activated.
11. The method according to claim 10 , wherein said transcription factor is constitutively activated.
12. The method according to claim 9 , wherein said cell is a malignant cell.
13. The method according to claim 9 , wherein said cell is a leukemia cell or a carcinoma cell.
14. The method according to claim 9 , wherein said transcription factor is a member of the STAT family of transcription factors.
15. The method according to claim 9 , wherein said transcription factor is STAT5.
16. The method according claim 1 , wherein said oligonucleotide comprises two or more copies of said nucleotide sequence.
17. The method according claim 1 , wherein said oligonucleotide consists of the nucleotide sequence AGATTTCTAGGAATTCAAATC (SEQ ID NO:1).
18. The method according to claim 9 , wherein said oligonucleotide comprises two or more copies of said nucleotide sequence.
19. The method according to claim 9 , wherein said oligonucleotide consists of the nucleotide sequence AGATTTCTAGGAATTCAAATC (SEQ ID NO:1).
20. The method according to claim 7 , wherein said leukemia is acute myeloid leukemia or chronic myeloid leukemia.
21. The method according to claim 7 , wherein said carcinoma is a carcinoma of the head, neck, or breast.
22. The method according to claim 1 , wherein said composition is administered orally, subcutaneously, or parenterally.
23. The method according to claim 22 , wherein said composition is administered intravenously, intraarterially, intramuscularly, intraperitoneally, or intranasally.
24. The method according to claim 1 , wherein said oligonucleotide is modified to increase resistance of said oligonucleotide to nucleases.
25. The method according to claim 9 , wherein said oligonucleotide is modified to increase resistance of said oligonucleotide to nucleases.