IP Library Granted Patent US 10,786,471
Granted Patent B2
US 10,786,471 · App. 15/890,220 · Granted Sep 29, 2020

Methods and products related to glutaminase inhibitors

Inventors: Alexander Muir (Cambridge, MA); Matthew Vander Heiden (Cambridge, MA); Laura Danai (Brighton, MA); Dan Yi Gui (Cambridge, MA)
Assignee: Massachusetts Institute of Technology
A61K31/198A61K9/0053A61K31/225A61K31/255A61K31/277A61K31/501A61K31/554A61K31/69A61K31/7105A61K38/1709A61K45/00A61K45/06A61P35/00G01N33/6893G01N2333/47
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Quick Facts
Patent No.
US 10,786,471
App. No.
15/890,220
Granted
Sep 29, 2020
Kind
B2
Abstract

The invention relates to methods and related compositions for enhancing cancer therapy and in particular glutaminase inhibitor therapy. The methods involve methods for identifying patients susceptible to glutaminase inhibitor therapy as well as sensitizing patients to glutaminase inhibitor therapy.

Claims (36)

1. A method of treating a subject, comprising

administering to a subject having cancer a glutaminase inhibitor and cystine in an effective amount to treat the subject.

2. The method of claim 1 , wherein the glutaminase inhibitor and cystine are administered together in a single formulation.

3. The method of claim 1 , wherein the glutaminase inhibitor and cystine are administered in separate formulations.

4. The method of claim 1 , wherein the cystine is administered before the glutaminase inhibitor.

5. The method of claim 1 , wherein the cystine is L-cystine or L-cysteine.

6. The method of claim 1 , wherein the cystine is administered to the subject as a cysteine formulation or as a cystine formulation.

7. The method of claim 1 , wherein the cystine is administered in an amount to produce a 50-300 micromolar concentration in blood of the subject.

8. The method of claim 1 , wherein the cystine is administered in an amount to produce a 100-150 micromolar concentration in blood of the subject.

9. The method of claim 1 , wherein the cystine is administered in an amount greater than 0.5 mmol/kg.

10. The method of claim 1 , further comprising determining whether a cystine/glutamate transporter, SLC7A11, is expressed in a cancer cell of the subject, wherein if the SLC7A11 is expressed in the cancer cell, the cancer cell is sensitive to glutaminase inhibitor therapy.

11. The method of claim 1 , wherein the subject has low levels or no expression of SLC7A11.

12. The method of claim 1 , wherein the subject has high levels of SLC7A11.

13. The method of claim 1 , further comprising administering a SLC7A11 inducer to the subject.

14. A method for enhancing a glutaminase inhibitor therapy in a subject, comprising administering to a subject receiving glutaminase inhibitor therapy, cystine in an effective amount to sensitize the subject to the glutaminase inhibitor therapy.

15. The method of claim 14 , wherein the cystine is administered in an amount to produce a 100-150 micromolar concentration in blood of the subject.

16. The method of claim 14 , wherein the cystine is administered in an amount greater than 0.5 mmol/kg.

17. The method of claim 14 , further comprising determining whether a cystine/glutamate transporter, SLC7A11, is expressed in a cancer cell of the subject, wherein if the SLC7A11 is expressed in the cancer cell, the cancer cell is sensitive to glutaminase inhibitor therapy.

18. The method of claim 1 , wherein the cystine is L-cystine or L-cysteine.

19. A method for enhancing a glutaminase inhibitor therapy in a subject, comprising administering to a subject receiving glutaminase inhibitor therapy a SLC7A11 inducer in an effective amount to induce expression of SLC7A11 in a cancer cell of the subject, thereby sensitizing the subject to the glutaminase inhibitor therapy.

20. The method of claim 19 , wherein the SLC7A11 inducer is a small molecule Nrf2 activator.

21. The method of claim 19 , wherein the SLC7A11 inducer is KI-696.

22. The method of claim 19 , wherein the SLC7A11 inducer is dimethyl fumarate.

23. The method of claim 19 , wherein the SLC7A11 inducer is CDDO-Me.

24. The method of claim 19 , wherein the SLC7A11 inducer is AI-3.

25. The method of claim 19 , wherein the SLC7A11 inducer is a miRNA.

26. The method of claim 19 , wherein the SLC7A11 inducer is VEDA-1209.

27. The method of claim 19 , wherein the SLC7A11 inducer is a nucleic acid encoding SLC7A11.

28. The method of claim 19 , further comprising administering cystine or cysteine to the subject.

29. The method of claim 19 , further comprising determining whether SLC7A11 is expressed in a cancer cell of the subject, wherein if the SLC7A11 is expressed in the cancer cell, the cancer cell is sensitive to glutaminase inhibitor therapy.

30. A method for detecting the presence or absence of a cystine/glutamate transporter in a cancer cell, comprising:

(a) obtaining a cancer cell from a human subject; and

(b) detecting whether a cystine/glutamate transporter, SLC7A11, is expressed in the cancer cell, wherein if the SLC7A11 is expressed in the cancer cell, the cancer cell is sensitive to glutaminase inhibitor therapy,

wherein the expression level of SLC7A11 is determined using PET imaging using a PET reagent, 18 F-propyl-glutamate, and

wherein the subject is administered cystine or cysteine in an effective amount to sensitize the subject to glutaminase inhibitor therapy.

31. The method of claim 30 , further comprising administering to the subject an SLC7A11 inducer in an effective amount to sensitize the subject to glutaminase inhibitor therapy.

Assignments (2)
CONFIRMATORY LICENSE Recorded Apr 24, 2018
From: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 046006/0185 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 29, 2018
From: MUIR, ALEXANDER; HEIDEN, MATTHEW VANDER; DANAI, LAURA; GUI, DAN YI
To: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
Reel/Frame 045382/0250 →
Continuity (2)
Provisional Application 62455463 · Feb 6, 2017
Related Publication 20180221321A1 · Aug 9, 2018