IP Library Granted Patent US 8,664,192
Granted Patent B2
US 8,664,192 · App. 13/414,084 · Granted Mar 4, 2014

Mutator activity induced by microRNA-155 (

Inventor: Carlo M. Croce (Columbus, OH)
Assignee: The Ohio State University
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 8,664,192
App. No.
13/414,084
Granted
Mar 4, 2014
Kind
B2
Abstract

Methods of reducing spontaneous mutation rate of a cell in a subject in need thereof by reducing endogenous levels of miR-155 are described.

Claims (27)

1. A method for modulating WEE1 kinase expression levels in an inflammation-related solid cancer target cell, comprising: administering a microRNA-155 (miR-155) antagonist to the target cell in an amount sufficient to modulate WEE1 kinase levels, and wherein the WEE1 levels are increased after administration.

2. The method of claim 1 , wherein the miR-155 antagonist comprises a modified oligonucleotide consisting of 12 to 30 linked nucleosides, wherein the nucleobase sequence of the modified oligonucleotide is complementary to a sequence at least 80% identical to mature miR-155, pre-miR-155, a miR-155 seed sequence, or a sequence fully complementary to the sequence of mature miR-155, pre-miR-155, or miR-155.

3. The method of claim 1 , wherein administering a miR-155 antagonist comprises: administering an antisense miR-155 expression vector to a target cell; and expressing an antisense miR-155 in the target cell.

4. The method of claim 1 , wherein the target cell is a breast cancer or precancerous cell.

5. The method of claim 1 , wherein the target cell is a colon cancer or precancerous cell.

6. The method of claim 1 , wherein the target cell is a gastric cancer or precancerous cell.

7. The method of claim 1 , wherein the target cell is a lung cancer or precancerous cell.

8. The method of claim 2 , wherein the modified oligonucleotide has no more than two mismatches to the nucleobase sequence of mature miR-155.

9. The method of claim 1 , comprising contacting the target cell with an antisense miR-155 inhibitory RNA (155-I), and wherein the WEE1 levels are increased after 155-I treatment.

10. A method of reducing spontaneous mutation rate of an inflammation-related solid cancer target cell in a subject in need thereof, comprising: contacting the target cell with an antisense miR-155 inhibitory RNA (155-I) in an amount sufficient to increase WEE1 levels, wherein the WEE1 levels are increased after 155-I treatment.

11. The method of claim 10 , wherein the miR-155 inhibitory RNA (155-I) comprises a miR-155 antagonist compound.

12. The method of claim 10 , wherein the miR-155 inhibitory RNA (155-I) binds to at least one oligonucleotide selected from the group consisting of:

a mature miR-155 oligonucleotide, a pre-miR-155 oligonucleotide, and a miR-155 seed sequence.

13. The method of claim 12 , wherein the miR-155 inhibitory RNA comprises a modified oligonucleotide consisting of 12 to 30 linked nucleosides, wherein the nucleobase sequence of the modified oligonucleotide is complementary to a sequence at least 80% identical to mature miR-155, pre-miR-155, a miR-155 seed sequence, or a sequence fully complementary to the sequence of mature miR-155, pre-miR-155, or miR-155.

14. The method of claim 10 , wherein contacting the cell comprises: administering an antisense miR-155 expression vector to the target cell; and expressing an antisense miR-155 in the target cell.

15. The method of claim 10 , wherein contacting the cell comprises: administering a miR-155 inhibitory RNA (155-I) expression vector to the target cell; and expressing 155-I in the target cell.

16. The method of claim 15 , wherein the miR-155 inhibitory RNA (155-I) expression vector comprises a nucleic acid sequence encoding 155-I operably linked to a promoter.

17. The method of claim 10 , wherein the cell is a breast cancer or precancerous cell.

18. The method of claim 10 , wherein the cell is a colon cancer or precancerous cell.

19. The method of claim 10 , wherein the cell is a gastric cancer or precancerous cell.

20. The method of claim 10 , wherein the cell is a lung cancer or precancerous cell.

21. The method of claim 13 , wherein the modified oligonucleotide has no more than two mismatches to the nucleobase sequence of mature miR-155.

22. The method of claim 10 , wherein the subject is human.

23. A method of preventing the onset of an inflammatory-related breast cancer, comprising: normalizing WEE1 levels by reducing inflammatory-related up-regulation of miR-155 in a subject in need thereof, by administering an antisense miR-155 inhibitory RNA (155-I) to a breast cell such that the resulting expression of miR-155 is normalized or elevated by no more than two-fold as compared with a control level of miR-155 expression, and wherein WEE1 levels are increased after 155-I treatment.

24. The method of claim 10 , wherein the cell further comprises a cell exhibiting at least one mutation selected from the group comprising: the mutations listed in FIG. 12 (SEQ ID NOS: 9-123).

25. The method of claim 1 , wherein the administration of the miR-155 antagonist reduces the miR-155 level in the target cell from greater than four-fold to less than two-fold as compared with a control level of miR-155, wherein the control level is derived from a non-cancerous cell, and wherein the WEE1 levels are increased after miR-155 antagonist administration.

26. The method of claim 10 , wherein the administration of the 155-I reduces the miR-155 level in the cancer cell from greater than four-fold to less than two-fold as compared with a control level of miR-155, wherein the control level is derived from a non-cancerous cell, and wherein the WEE1 levels are increased after 155-I administration.

Assignments (2)
CONFIRMATORY LICENSE Recorded Nov 5, 2012
From: THE OHIO STATE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029244/0395 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 5, 2012
From: CROCE, CARLO M.
To: THE OHIO STATE UNIVERSITY
Reel/Frame 027998/0613 →
Continuity (2)
Provisional Application 61449854 · Mar 7, 2011
Related Publication 20130065938A1 · Mar 14, 2013