IP Library Granted Patent US 9,801,853
Granted Patent B2
US 9,801,853 · App. 13/639,258 · Granted Oct 31, 2017

Methods for identifying and using inhibitors of casein kinase 1 epsilon isoform for inhibiting the growth and/or proliferation of MYC-driven tumor cells

Inventors: Carla Grandori (Seattle, WA); Masafumi Toyoshima (Seattle, WA)
Assignee: Fred Hutchinson Cancer Research Center
A61K31/404A61K31/506A61K31/519A61K33/24
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Quick Facts
Patent No.
US 9,801,853
App. No.
13/639,258
Granted
Oct 31, 2017
Kind
B2
Abstract

In one aspect, the invention provides a method for inhibiting the growth and/or proliferation of a myc-driven tumor cell comprising the step of contacting the tumor cells with a CSNK1ε inhibitor. In another aspect, the invention provides a method of treating a subject suffering from a tumor comprising myc-driven tumor cells, comprising administering to the subject an amount of a composition comprising a CSNK1ε inhibitor effective to inhibit the growth and/or proliferation of the tumor cells.

Claims (21)

1. A method for inhibiting the growth and/or proliferation of a cisplatin resistant ovarian tumor cell having an amplified c-myc gene, comprising the step of contacting the cisplatin resistant ovarian tumor cell having the amplified c-myc gene with a casein kinase 1 epsilon (CSNK1ε) inhibitor.

2. The method of claim 1 , wherein the tumor cell is contacted in vitro.

3. The method of claim 1 , wherein the tumor cell is contacted in vivo in a mammalian subject.

4. The method of claim 1 , wherein the CSNK1ε inhibitor is a small molecule inhibitor.

5. The method of claim 4 , wherein the CSNK1ε inhibitor is selected from the group consisting of IC261, PF-4800567, and PF-670462.

6. A method of treating a subject suffering from a cisplatin resistant ovarian tumor comprising cisplatin resistant ovarian tumor cells having an amplified c-myc gene, comprising administering to the subject an amount of a composition comprising a casein kinase 1 epsilon (CSNK1ε) inhibitor effective to inhibit the growth and/or proliferation of the cisplatin resistant ovarian tumor cells having the amplified c-myc gene.

7. The method of claim 6 , wherein the subject is further provided one or more additional anti-cancer therapies.

8. The method of claim 7 , wherein the additional anti-cancer therapy comprises cisplatin.

9. The method of claim 6 , wherein the CSNK1ε inhibitor is a small molecule inhibitor.

10. The method of claim 9 , wherein the CSNK1ε inhibitor is selected from the group consisting of IC261, PF-4800567, and PF-670462.

11. The method of claim 6 , further comprising the step of determining whether the tumor comprises tumor cells having an amplified c-myc gene prior to administering to said subject suffering from a tumor comprising tumor cells having the amplified c-myc gene said composition comprising a CSNK1e inhibitor.

12. A method of treating cisplatin resistance in ovarian tumor cells comprising the steps of: (i) determining whether said tumor cells overexpress c-Myc and (ii) subsequently administering an effective amount of a casein kinase 1 epsilon (CSNK1ε) inhibitor to said cisplatin resistant ovarian tumor cells.

13. The method of claim 12 , wherein the CSNK1ε inhibitor is a small molecule inhibitor.

14. The method of claim 13 , wherein the small molecule inhibitor is IC261.

15. The method of claim 12 , wherein the subject is further provided one or more additional anti-cancer therapies.

16. The method of claim 15 , wherein the additional anti-cancer therapy comprises cisplatin.

17. A method of treating cisplatin resistance in ovarian tumor cells comprising the steps of: (i) determining whether said tumor cells have an amplified c-myc gene and (ii) subsequently administering an effective amount of a casein kinase 1 epsilon (CSNK1ε) inhibitor to said cisplatin resistant ovarian tumor cells.

18. The method of claim 17 , wherein the CSNK1ε inhibitor is a small molecule inhibitor.

19. The method of claim 18 , wherein the small molecule inhibitor is IC261.

20. The method of claim 17 , wherein the subject is further provided one or more additional anti-cancer therapies.

21. The method of claim 20 , wherein the additional anti-cancer therapy comprises cisplatin.

Assignments (5)
MERGER AND CHANGE OF NAME Recorded May 23, 2022
From: FRED HUTCHINSON CANCER RESEARCH CENTER; SEATTLE CANCER CARE ALLIANCE
To: SEATTLE CANCER CARE ALLIANCE
Reel/Frame 060163/0887 →
CHANGE OF NAME Recorded May 23, 2022
From: SEATTLE CANCER CARE ALLIANCE
To: FRED HUTCHINSON CANCER CENTER
Reel/Frame 060389/0005 →
CONFIRMATORY LICENSE Recorded Jan 13, 2017
From: FRED HUTCHINSON CANCER RESEARCH CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 041370/0043 →
CONFIRMATORY LICENSE Recorded Jan 12, 2017
From: FRED HUTCHINSON CANCER RESEARCH CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 041345/0880 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 27, 2012
From: GRANDORI, CARLA; TOYOSHIMA, MASAFUMI
To: FRED HUTCHINSON CANCER RESEARCH CENTER
Reel/Frame 029534/0422 →
Continuity (2)
Provisional Application 61321414 · Apr 6, 2010
Related Publication 20130115309A1 · May 9, 2013