IP Library Granted Patent US 10,876,119
Granted Patent B2
US 10,876,119 · App. 16/022,652 · Granted Dec 29, 2020

Reduced size self-delivering RNAI compounds

Inventors: Anastasia Khvorova (Westborough, MA); William Salomon (Worcester, MA); Joanne Kamens (Newton, MA); Dmitry Samarsky (Westborough, MA); Tod M. Woolf (Sudbury, MA); James Cardia (Franklin, MA)
Assignee: Phio Pharmaceuticals Corp.
C12N15/1136C12N15/111C12N15/113C12N15/1137C12N2310/14C12N2310/315C12N2310/321C12N2310/322C12N2310/3231C12N2310/3341C12N2310/3515C12N2310/3519C12N2310/3521C12N2320/32C12N2320/51C12N2320/53
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Quick Facts
Patent No.
US 10,876,119
App. No.
16/022,652
Granted
Dec 29, 2020
Kind
B2
Abstract

The present invention relates to RNAi constructs with minimal double-stranded regions, and their use in gene silencing. RNAi constructs associated with the invention include a double stranded region of 8-14 nucleotides and a variety of chemical modifications, and are highly effective in gene silencing. The RNAi constructs may be, for instance, miRNA constructs that are miRNA modulators.

Claims (24)

1. An isolated nucleic acid molecule comprising

a guide strand of 18-23 nucleotides in length that has complementarity to a miRNA sequence, and

a passenger strand of 8-16 nucleotides in length,

wherein the guide strand and the passenger strand form the nucleic acid molecule such that the nucleic acid has a double stranded region and a single stranded region, wherein the single stranded region is the 3′ end of the guide strand and comprises at least two phosphorothioate modifications, and wherein at least 50% of the pyrimidines in the nucleic acid molecule are modified.

2. The nucleic acid molecule of claim 1 , wherein the nucleotide in position one of the guide strand has a 2′-O-methyl modification.

3. The nucleic acid molecule of claim 2 , wherein the nucleotide in position one of the guide strand is a 5P-2′O-methyl U.

4. The nucleic acid molecule of claim 1 , wherein at least 60%, at least 80%, at least 90%, or 100% of the pyrimidines in the nucleic acid molecule are modified.

5. The nucleic acid molecule of claim 1 , wherein modified pyrimidines are 2′fluoro or 2′O methyl modified.

6. The nucleic acid molecule of claim 1 , wherein at least one U or C includes a hydrophobic modification.

7. The nucleic acid molecule of claim 6 , wherein the hydrophobic modification is a methyl or ethyl hydrophobic base modification.

8. The nucleic acid molecule of claim 1 , wherein the guide strand contains 6-8 phosphorothioate modifications.

9. The nucleic acid molecule of claim 1 , wherein the 3′ terminal 10 nucleotides of the guide strand include at least eight phosphorothioate modifications.

10. The nucleic acid molecule of claim 1 wherein the guide strand includes 4-14 phosphate modifications.

11. The nucleic acid molecule of claim 1 , wherein the single stranded region of the guide strand is 6 nucleotides long.

12. The nucleic acid molecule of claim 1 , wherein the double stranded region is 16 nucleotides long.

13. The nucleic acid molecule of claim 1 , wherein the nucleic acid molecule has one end that is blunt or includes a one nucleotide overhang.

14. The nucleic acid molecule of claim 1 , wherein the passenger strand is linked at the 3′ end to a lipophilic group.

15. The nucleic acid molecule of claim 14 , wherein the lipophilic group is a sterol.

16. The nucleic acid molecule of claim 1 , wherein the nucleic acid molecule is an miRNA mimic and wherein the miRNA sequence to which the guide strand is complementary is a miRNA recognition element.

17. The nucleic acid molecule of claim 16 , wherein the miRNA mimic is a mimic of an miRNA selected from the group consisting of miR21, miR 139, miR 7, miR29, miR 122, miR 302-367 cluster, miR 221, miR-96, miR 126, miR 225 and miR 206.

18. A method of modulating miRNA-mediated gene expression in a subject comprising:

administering to a subject an effective amount for modulating miRNA-mediated gene expression of the isolated nucleic acid molecule of claim 1 .

19. The method of claim 18 , wherein the administration is systemic, intravenous, intraperitoneal, intradermal, topical, or intraocular.

20. The method of claim 18 , wherein the subject is a human.

Assignments (2)
CHANGE OF NAME Recorded Dec 7, 2018
From: RXI PHARMACEUTICALS CORPORATION
To: PHIO PHARMACEUTICALS CORP.
Reel/Frame 048380/0009 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 15, 2018
From: KHVOROVA, ANASTASIA; SALOMON, WILLIAM; KAMENS, JOANNE; SAMARSKY, DMITRY; WOOLF, TOD M.; CARDIA, JAMES
To: RXI PHARMACEUTICALS CORPORATION
Reel/Frame 047228/0869 →
Continuity (6)
Continuation 13069780 · Mar 23, 2011
Continuation In Part 13120342
Provisional Application 61224031 · Jul 8, 2009
Provisional Application 61149946 · Feb 4, 2009
Provisional Application 61192954 · Sep 22, 2008
Related Publication 20190161757A1 · May 30, 2019
Cited By (2)
US 12,544,344 US 12,709,752