Methods for treating brain metastasis

Patent metadata

Field	Value
Publication number	US-10413522-B2
Application number	US-201715462253-A
Country	US
Kind code	B2
Filing date	Mar 17, 2017
Priority date	Sep 19, 2014
Publication date	Sep 17, 2019
Grant date	Sep 17, 2019

Abstract

The present invention relates to methods for treating brain metastasis by inhibiting gap junction functionality. It is based, at least in part, on the discovery that cancer cells expressing Protocadherin 7 and Connexin 43 form gap junctions with astrocytes that promote the growth of brain metastases, and that inhibition of Protocadherin 7 and/or Connexin 43 expression in cancer cells reduce progression of brain metastases. It is further based on the discovery that treatment with gap junction inhibitors tonabersat and meclofenamate inhibited progression of brain metastatic lesions and enhanced the anti-cancer activity of the conventional chemotherapeutic agent, carboplatin.

First claim

What is claimed is:

1. A method for treating a subject having a cancer comprising administering, to the subject, an amount of a gap junction inhibitor that inhibits and/or prevents metastatic progression of the cancer in the brain, wherein the gap junction inhibitor is selected from the group consisting of tonabersat, meclofenamate, a Protocadherin 7 inhibitor, a Connexin 43 inhibitor and a combination thereof.

2. The method of claim 1 , wherein the cancer is selected from the group consisting of breast cancer and lung cancer.

3. The method of claim 1 further comprising administering, to the subject, a therapeutically effective amount of an anti-cancer agent.

4. The method of claim 3 , wherein the anti-cancer agent is carboplatin.

5. The method of claim 1 , wherein the subject was known to have one or more brain metastases prior to treatment.

6. The method of claim 1 , wherein the subject was not known to have a brain metastasis prior to treatment.

7. The method of claim 1 , wherein one or more cancer cells of the subject express Connexin 43 and/or Protocadherin 7.

8. A method for treating brain metastasis in a subject having a cancer, comprising administering, to the subject, a therapeutically effective amount of a gap junction inhibitor for treating the brain metastasis in the subject, wherein the gap junction inhibitor is selected from the group consisting of tonabersat, meclofenamate, a Protocadherin 7 inhibitor, a Connexin 43 inhibitor and a combination thereof.

9. The method of claim 8 , wherein the cancer is selected from the group consisting of breast cancer and lung cancer.

10. The method of claim 8 , further comprising administering, to the subject, a therapeutically effective amount of an anti-cancer agent.

11. The method of claim 10 , wherein the anti-cancer agent is carboplatin.

12. The method of claim 8 , wherein one or more cancer cells of the subject express Connexin 43 and/or Protocadherin 7.

13. A method of treatment, wherein the risk of detectable metastasis of a cancer to the brain is reduced, comprising administering, to a subject having the cancer, a therapeutically effective amount of a gap junction inhibitor for reducing the risk of detectable metastasis of the cancer to the brain of the subject, wherein the gap junction inhibitor is selected from the group consisting of tonabersat, meclofenamate, a Protocadherin 7 inhibitor, a Connexin 43 inhibitor and a combination thereof.

14. The method of claim 13 , wherein the cancer is selected from the group consisting of breast cancer and lung cancer.

15. The method of claim 13 , further comprising administering, to the subject, a therapeutically effective amount of an anti-cancer agent.

16. A method of treatment, wherein the growth of a brain tumor in a subject is inhibited, comprising:
a) obtaining one or more tumor cells from a subject with a brain tumor;
b) exposing the tumor cells obtained from the subject to a gap junction inhibitor;
c) determining whether the tumor cells obtained from the subject exhibit a decrease in cGAMP when exposed to a gap junction inhibitor relative to the cGAMP level in the absence of the inhibitor, where a decrease in cGAMP is indicative of therapeutic benefit; and
d) (i) where a decrease in cGAMP is observed, treating the subject with the gap junction inhibitor or (ii) where a decrease in cGAMP is not observed, treating the subject with another modality.

17. The method of claim 1 , wherein the gap junction inhibitor is meclofenamate or a salt form thereof.

18. The method of claim 1 , wherein the gap junction inhibitor is a sodium salt form of meclofenamate.

Assignees

• Memorial Sloan Kettering Cancer Center

Inventors

• Massague Joan
• Boire Adrienne
• Chen Qing

Classifications

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61P35/04

  specific for metastasis · CPC title

• A61P35/00

  Antineoplastic agents · CPC title

• A61K31/555

  containing heavy metals, e.g. hemin, hematin, melarsoprol · CPC title

• A61K31/282

  Platinum compounds · CPC title