IP Library › Granted Patent US 11,643,659
Granted Patent B2
US 11,643,659 · App. 16/786,793 · Granted May 9, 2023

Conditional-siRNAS and uses thereof in treating acute myeloid leukemia

Inventors: Guido Marcucci (Duarte, CA); Ya-Huei Kuo (Duarte, CA); Si-ping Han (Duarte, CA); Lisa Scherer (Duarte, CA); William A. Goddard, III (Pasadena, CA); John Rossi (Duarte, CA)
Assignees: CITY OF HOPE; CALIFORNIA INSTITUTE OF TECHNOLOGY
C12N15/1135C12N2310/14C12N2310/3519C12N2320/50
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,643,659
App. No.
16/786,793
Granted
May 9, 2023
Kind
B2
Abstract

Disclosed herein are conditional siRNAs activatable by CBFβ-MYH11 oncogenic gene and use thereof for treating conditions such as acute myeloid leukemia (AML). The conditional siRNAs target MCL-1 or HDAC8.

Claims (30)

1. A conditional RNA-sensor complex comprising:

a sensor strand comprising at least one toehold segment, wherein the toehold segment binds a pathological biomarker associated with acute myeloid leukemia (AML); and

a double stranded pro-RNA molecule comprising

a guide strand comprising an RNA molecule that binds a therapeutic target molecule; and

a core strand comprising

a first portion comprising a passenger strand that is fully or partially complimentary to and binds the guide strand;

a second portion comprising a first protection segment that is fully or partially complimentary to and binds the sensor strand; and

a first linker that joins a first end of the passenger strand to the first protection segment,

wherein the sensor strand comprises a sequence having at least 95% homology to SEQ ID NO:1, and

wherein the double stranded pro-RNA molecule is an RNA interference (RNAi) molecule and the therapeutic target molecule is MCL-1 or HDAC8.

2. The conditional RNA-sensor complex of claim 1 , wherein the core strand further comprises a third portion comprising a second protection segment that is fully or partially complimentary to and binds the sensor strand, and a second linker that joins a second end of the passenger strand to the second protection segment.

3. The conditional RNA-sensor complex of claim 1 , wherein the toehold segment is an aptamer.

4. The conditional RNA-sensor complex of claim 1 , wherein the sensor strand is displaced from the double stranded pro-RNA molecule when the pathological biomarker binds the toehold segment and the resulting double stranded pro-RNA molecule is a substrate for Dicer.

5. The conditional RNA-sensor complex of claim 1 , wherein the pathological biomarker comprises a molecule that encodes a portion of CBFβ-MYH11.

6. The conditional RNA-sensor complex of claim 1 , wherein the sensor strand comprises SEQ ID NO:1.

7. The conditional RNA-sensor complex of claim 1 , wherein the guide strand comprises SEQ ID NO:2 or SEQ ID NO:3.

8. The conditional RNA-sensor complex of claim 2 , wherein the core strand comprises

a passenger strand;

a first linker that joins a 3′ end of the passenger strand to the first protection segment; and

a second linker that joins a 5′ end of the passenger strand to the second protection segment.

9. The conditional RNA-sensor complex of claim 8 , wherein the core strand comprises SEQ ID NOs:4, 5 or 6.

10. The conditional RNA-sensor complex of claim 6 , wherein the sensor strand, the guide strand and/or the core strand further comprises one or more chemical modifications to the RNA sequence, wherein the one or more chemical modifications are selected from a locked nucleic acid (LNA) modification, a peptide nucleic acid (PNA) modification, a 2′-O-methyl modification, morpholino modification, a phosphorothioate modification, a terminal modification, or a linker modification.

11. The conditional RNA-sensor complex of claim 10 , wherein the sensor strand comprises SEQ ID NO:7.

12. The conditional RNA-sensor complex of claim 10 , wherein the sensor strand comprises SEQ ID NO:8.

13. The conditional RNA-sensor complex of claim 1 , wherein the core strand comprises a sequence having at least 95% homology to SEQ ID NOs:4, 5 or 6, and the guide strand comprises a sequence having at least 95% homology to SEQ ID NO:2.

14. The conditional RNA-sensor complex of claim 13 , wherein the sensor strand, the guide strand and/or the core strand further comprises one or more chemical modifications to the RNA sequence, wherein the one or more chemical modifications are selected from a locked nucleic acid (LNA) modification, a peptide nucleic acid (PNA) modification, a 2′-O-methyl modification, morpholino modification, a phosphorothioate modification, a terminal modification, or a linker modification.

15. A pharmaceutical composition comprising:

a conditional RNA-sensor complex of claim 1 ; and

a pharmaceutically acceptable carrier or excipient.

16. A method of treating acute myeloid leukemia (AML) comprising administering a therapeutically effective amount of a conditional RNA-sensor complex of claim 1 to a subject suffering from AML.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 14, 2022
From: GODDARD, WILLIAM A., III
To: CALIFORNIA INSTITUTE OF TECHNOLOGY
Reel/Frame 060196/0988 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 14, 2022
From: KUO, YA-HUEI; HAN, SI-PING; SCHERER, LISA; ROSSI, JOHN; MARCUCCI, GUIDO
To: CITY OF HOPE
Reel/Frame 060197/0018 →
Continuity (3)
Continuation PCTUS2018046383 · Aug 10, 2018
Provisional Application 62543812 · Aug 10, 2017
Related Publication 20210123060A1 · Apr 29, 2021
Cited By (2)
US 12,385,041 US 12,674,164