IP Library › Granted Patent US 8,933,051
Granted Patent B2
US 8,933,051 · App. 13/876,725 · Granted Jan 13, 2015

Treatment of B-cell lymphoma with microRNA

Inventors: Vanessa Craig (Zurich, CH); Anne Mueller (Dubendorf, CH)
Assignee: University of Zurich
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Quick Facts
Patent No.
US 8,933,051
App. No.
13/876,725
Granted
Jan 13, 2015
Kind
B2
Abstract

The invention relates to microRNA-34a and related microRNAs for use in the treatment of B-cell lymphoma. Likewise it relates to microRNA-34a for use in the preparation of a medicament for the treatment of B-cell lymphoma, and for a method of treatment of B-cell lymphoma comprising administering microRNA-34a. These claims are based on the observation that microRNA-34a shows strong anti-proliferative effects when overexpressed in diffuse large B-cell lymphoma (gDLBCL) cell lines, or when delivered intratumorally or systemically in xenograft models of DLBCL.

Claims (19)

1. A method of treating a B-cell lymphoma, the method comprising administering to a patient a therapeutically effective amount of a microRNA, wherein the B cell lymphoma is diffuse large B-cell lymphoma and wherein the microRNA is a member of the miR-34 family.

2. The method of claim 1 , wherein the gastric B-cell lymphoma is high-grade gastric diffuse large B-cell lymphoma.

3. The method of claim 1 , wherein the microRNA is miR-34a, miR-34b, miR-34c-5p or miR-34c-3p.

4. The method of claim 1 , further comprising administering another active ingredient selected from cyclophosphamide, hydroxydaunorubicin, vincristine, prednisone/prednisolone, rituximab, or combinations thereof.

5. A method of treating gastric B-cell lymphoma or diffuse large B-cell lymphoma, the method comprising administering a therapeutically effective amount of a microRNA which is a member of the miR-34 family.

6. The method of claim 5 , wherein the microRNA is miR-34a.

7. A method of treating a diffuse large B-cell lymphoma, comprising administering a therapeutically effective amount of a microRNA, wherein the diffuse large B-cell lymphoma is characterized by an over-expression of FoxP1, and wherein the microRNA is a member of the miR-34 family.

8. The method of claim 7 , wherein the B-cell lymphoma is diffuse large B-cell lymphoma.

9. The method of claim 7 , wherein the B-cell lymphoma is gastric B-cell lymphoma.

10. The method of claim 7 , wherein the microRNA is miR-34a, miR-34b, miR-34c-5p or miR-34c-3p.

11. The method of claim 7 , further comprising administering another active ingredient selected from cyclophosphamide, hydroxydaunorubicin, vincristine, prednisone/prednisolone, rituximab, or combinations thereof.

12. A method of treating gastric B-cell lymphoma or diffuse large B-cell lymphoma, the method comprising administering a therapeutically effective amount of a microRNA which is a member of the miR-34 family.

13. The method of claim 12 , wherein the microRNA is miR-34a.

14. The method of claim 7 , wherein the microRNA is miR-34a and the B-cell lymphoma is diffuse large B-cell lymphoma.

15. The method of claim 12 , wherein the microRNA is miR-34a and the B-cell lymphoma is diffuse large B-cell lymphoma.

16. The method of claim 1 , wherein the microRNA is miR-34a.

17. The method of claim 7 , wherein the microRNA is miR-34a.

18. The method of claim 1 , wherein the diffuse large B-cell lymphoma is gastric diffuse large B-cell lymphoma.

19. The method of claim 5 , wherein the diffuse large B-cell lymphoma is gastric diffuse large B-cell lymphoma.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2015
From: CRAIG, VANESSA; MUELLER, ANNE
To: UNIVERSITY OF ZURICH
Reel/Frame 034683/0008 →
Priority Claims (1)
EP 10182950 · Sep 30, 2010 · regional
Continuity (1)
Related Publication 20130195858A1 · Aug 1, 2013