Polyamine transport inhibitors as novel therapeutics

Patent metadata

Field	Value
Publication number	US-9730902-B2
Application number	US-201514962195-A
Country	US
Kind code	B2
Filing date	Dec 8, 2015
Priority date	Jun 19, 2009
Publication date	Aug 15, 2017
Grant date	Aug 15, 2017

Abstract

Novel polyamine transport inhibitors have been synthesized and demonstrated to block the uptake of native polyamines into human cancer cells. A combination therapy of the transport inhibitor and DFMO (a drug which blocks polyamine biosynthesis) provided synergistic activity against a metastatic human colon cancer cell line. The strategy uses polyamine depletion and polyamine metabolism to generate reactive oxygen species within cells as a novel way to treat cancers. This approach may be implemented for widespread use in the treatment of diseases which rely upon polyamine transport activity for proliferation.

First claim

The invention claimed is:

1. A method for treating a disorder in a subject characterized by high polyamine content in tissues, the method comprising administering to a subject a pharmaceutical composition comprising compound 3d, 3e, 3f, 4a, 4b, 4c, 4d, 5a, 5b, 5c, 5d, 5e, 5f, 6a, 6b, 6c, 6d, 7a, 7b, 7c, 7d, 8a, 8b, 8c, 8d, 8e, 8f, 9a, 9b, 9c, 9d, 10a, 10b, 10c or 10d, or a pharmaceutically acceptable salt thereof in an amount effective to inhibit polyamine transporter activity in cells of the subject, wherein the disorder is colon cancer or pancreatic cancer.

2. The method of claim 1 , further comprising administering an additional chemotherapeutic agent in an amount effective to reduce cellular polyamine content.

3. The method of claim 1 , further comprising administering to a subject each of: (1) DMFO; and (2) sulindac; and (3) a SSAT inducing agent in an amount effective to inhibit polyamine transporter activity in cells of the subject, wherein the compound is compound 3-7 or a pharmaceutically acceptable salt thereof.

4. The method of claim 1 , wherein the compound is selected from 8-10 in an amount effective to inhibit the polyamine transporter activity in living cells.

5. The method of claim 1 , further comprising administering to the subject DFMO; and wherein the compound is selected from 8-10 or a pharmaceutically acceptable salt thereof, in an amount effective to inhibit the polyamine transporter activity in cells of the subject.

6. The method of claim 1 , further comprising administering DFMO to the subject.

7. The method of claim 1 , further comprising administering DFMO or Suldinac, or both, to the subject.

8. The method of claim 1 , wherein administering the pharmaceutical composition modulates the immune response in the mammal.

Assignees

• Phanstiel Iv Otto
• Archer Jennifer J
• Univ Central Florida Res Found Inc

Inventors

• Phanstiel Iv Otto
• Archer Jennifer J

Classifications

• A61P35/00

  Antineoplastic agents · CPC title

• A61P29/00

  Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] · CPC title

• C07C231/02

  from carboxylic acids or from esters, anhydrides, or halides thereof by reaction with ammonia or amines · CPC title

• C07C237/46

  having carbon atoms of carboxamide groups, amino groups and at least three atoms of bromine or iodine, bound to carbon atoms of the same non-condensed six-membered aromatic ring · CPC title

• C07C235/10

  having the nitrogen atom of at least one of the carboxamide groups bound to an acyclic carbon atom of a hydrocarbon radical substituted by nitrogen atoms not being part of nitro or nitroso groups · CPC title