RNA modulating oligonucleotides with improved characteristics for the treatment of neuromuscular disorders
The current invention provides an improved oligonucleotide and its use for treating, ameliorating, preventing, delaying and/or treating a human cis-element repeat instability associated genetic neuromuscular or neurodegenerative disorder.
1. A method for treating, delaying, ameliorating and/or preventing a spinocerebellar ataxia (SCA), spinal and bulbar muscular atrophy (SBMA), or dentatorubral-pallidoluysian atrophy (DRPLA) in a subject, comprising providing to the subject an antisense oligonucleotide comprising a 2′-O-methyl RNA nucleotide residue, having a backbone wherein at least one phosphate moiety is replaced by a phosphorothioate moiety, and comprising a repetitive nucleotide unit (XYG)m, wherein m is an integer from 4 to 12 and each X is C or 5-methylcytosine, and each Y is U or 5-methyluracil, wherein at least one X is 5-methylcytosine, wherein said oligonucleotide is able to hybridize to a (CAG)n repetitive nucleotide unit.
2. The method of claim 1 , wherein said oligonucleotide consists of a repetitive nucleotide unit (XYG)m, wherein m is an integer from 4 to 12 and each X is C or 5-methylcytosine, and each Y is U or 5-methyluracil, wherein at least one X is 5-methylcytosine and/or at least one Y is 5-methyluracil.
3. The method of claim 1 , wherein said oligonucleotide is such that each X is 5-methylcytosine and/or each Y is 5-methyluracil.
4. The method of claim 1 , wherein said oligonucleotide is such that m is 5 or 6 or 7 or 8 or 9 or 10 or 11 or 12.
5. The method of claim 4 , wherein said oligonucleotide comprises a repetitive nucleotide unit (XYG)7, wherein each X is 5-methylcytosine and each Y is a uracil (SEQ ID NO: 2).
6. The method of claim 4 , wherein said oligonucleotide is such that m is 7.
7. The method of claim 1 , wherein the sequence of said oligonucleotide comprises any of SEQ ID NO: 90, 96, 104-109, 111, 113, 115, and 117.
8. The method of claim 7 , wherein the base sequence of said oligonucleotide comprises SEQ ID NO:90.
9. The method of claim 1 , wherein said oligonucleotide is a single-stranded oligonucleotide.
10. The method of claim 1 wherein said oligonucleotide has a length of from 12 to 36 nucleotides.
11. The method of claim 1 , wherein said oligonucleotide remain in association to its target when there are up to 20% of mismatched nucleotides.
12. The method of claim 1 , wherein said oligonucleotide is at least 90% reverse complementary with said repetitive nucleotide unit.
13. The method of claim 1 , wherein said oligonucleotide has an improved parameter by comparison to a corresponding oligonucleotide comprising a 2′-O-methyl RNA nucleotide residue and having a backbone wherein at least one phosphate moiety is replaced by a phosphorothioate moiety, without a 5-methylcytosine, and/or a 5-methyluracil and/or a 2,6-diaminopurine.
14. The method of claim 1 , wherein said oligonucleotide reduces a detectable amount of mutant transcript and/or reduces the translation of said mutant transcript and thus the amount of mutant protein.
15. The method of claim 14 , wherein said reduction of mutant protein reduces protein aggregates in nucleus and/or cytoplasm.
16. The method of claim 1 , wherein said oligonucleotide is present in a composition.
17. The method of claim 16 , wherein said composition comprises at least one excipient that may further aid in enhancing the targeting and/or delivery of said composition and/or said oligonucleotide to a tissue and/or cell and/or into a tissue and/or cell.
18. The method of claim 1 , wherein said oligonucleotide preferentially hybridizes to a disease-associated or disease-causing transcript and leaves a function of a normal transcript relatively unaffected.
19. The method of claim 1 , wherein said subject has DRPLA, SBMA, or SCA type 1, 2, 3, 6, 7, 12 or 17.
20. The method of claim 19 , wherein
said SCA type 1 is caused by CAG repeat expansions in the transcripts of ATXN1 (SEQ ID NO:81),
said SCA type 2 is caused by CAG repeat expansions in the transcripts of ATXN2 (SEQ ID NO: 82),
said SCA type 3 is caused by CAG repeat expansions in the transcripts of ATXN3 (SEQ ID NO: 83),
said SCA type 6 is caused by CAG repeat expansions in the transcripts of CACNA1A (SEQ ID NO:84), said SCA type 7 is caused by CAG repeat expansions in the transcripts of ATXN7 (SEQ ID NO: 85),
said SCA type 12 is caused by CAG repeat expansions in the transcripts of PPP2R2B (SEQ ID NO: 86), and
said SCA type 17 is caused by CAG repeat expansions in the transcripts of TBP (SEQ ID NO: 87) genes.
21. The method of claim 1 , wherein said SBMA is caused by CAG repeat expansions in the transcripts of AR (SEQ ID NO: 88), and said DRPLA is caused by CAG repeat expansions in the transcripts of ATN1 (SEQ ID NO: 89) genes.
22. The method of claim 1 , wherein the antisense oligonucleotide is provided by intrathecal administration.
23. The method of claim 4 , wherein said oligonucleotide consists of a repetitive nucleotide unit (XYG)7, wherein each X is 5-methylcytosine and each Y is a uracil (SEQ ID NO: 2).
24. A method for treating, delaying, ameliorating and/or preventing a spinocerebellar ataxia (SCA) type 1 or type 3 in a subject, comprising providing to the subject an antisense oligonucleotide which consists of 2′-O-methyl RNA nucleotide residues and has a backbone wherein all phosphate moieties are replaced by a phosphorothioate moiety, and which comprises the base sequence of SEQ ID NO: 90.
25. The method of claim 23 , wherein the antisense oligonucleotide is provided by intrathecal administration.