Compositions and methods for inhibiting metastasis

Patent metadata

Field	Value
Publication number	US-10722528-B2
Application number	US-201916366469-A
Country	US
Kind code	B2
Filing date	Mar 27, 2019
Priority date	Mar 28, 2018
Publication date	Jul 28, 2020
Grant date	Jul 28, 2020

Abstract

Calprotectin inhibitors and derivatives thereof, and methods of using them for inhibiting or reducing metastatis and treating cancer are provided. The pharmaceutical formulations prepared from the compounds can be used in the treatment of cancer either as a single agent or in combination with at least one other cancer therapeutic, chemotherapeutic or anti-cancer agent.

First claim

We claim:

1. A method for inhibiting or reducing cancer cell metastasis in a subject in need thereof comprising administering to the subject a composition comprising at least one calprotectin inhibitor, in an amount effective to inhibit or reduce cancer cell metastasis, and a pharmaceutically acceptable excipient.

2. The method of claim 1 , wherein the calprotectin inhibitor is NSC37627, NSC60785, or NSC727038.

3. The method of claim 1 , further comprising administering to the subject a second cancer therapeutic selected from the group consisting of alkylating agents, cancer immunotherapeutic agents, chemotherapeutics, or cytotoxic/cytostatic agents.

4. The method of claim 3 , wherein the alkylating agent is selected from the group consisting of cyclophosphamide, chlorambucil, mechhlorethamine, cisplatin, oxaliplatin, carboplatin, temolozomide, melphalan, streptozocin, busulfan, bendamustine, and trabectedin.

5. The method of claim 3 , wherein the cancer immunotherapeutic agent is selected from the group consisting of alemtuzumab, trastuzumab, bevacizumab, cetuximab, ibritumomab tiuxetan, brentuximab vedotin, ado-trastuzumab emtansine, denileukin diftitox, and blinatumomab.

6. The method of claim 3 , wherein the cytotoxic/cytostatic agent is selected from the group consisting of 5-Fluorouracil, doxorubicin, daunorubicin, lonidamine, altretamine, prednimustine, dibromodulcitol, ranimustine, fotemustine, nedaplatin, temozolomide, hepaplatin, estramustine, improsulfan tosilate, trofosfamide, nimustine, dibrospidium chloride, pumitepa, lobaplatin, pemetrexed, bevacizumab, cetuximab, tositumonab, bortezomib, gefitinib, ibritumomab tiuxetan, imatinib mesylate, alemtuzumab, arsenic trioxide, gemtuzumab, temozolomide, valrubicin, tanstuzumab, capecitabine, rituximab, interferon-a, topotecan, gemcitabine, topotecan, docetaxel, tretinoin, navelbine, claribine, paclitaxel, bisantrene, mitox-antrone, and elinafide.

7. The method of claim 1 , wherein the effective amount of calprotectin inhibitor inhibits the induction of gMDSCs in the tumor microenvironment of the subject.

8. The method of claim 1 , wherein the cancer is selected from the group consisting of bladder, brain, cervical, colo-rectal, esophageal, kidney, liver, lung, nasopharangeal, pancreatic, prostate, skin, stomach, uterine, ovarian, testicular and hematologic cancers.

9. The method of claim 1 , wherein the cancer is pre-metastatic.

10. The method of claim 1 , wherein the cancer is metastatic.

11. The method of claim 1 , wherein the composition is administered parenterally.

12. The method of claim 1 , wherein the composition is administered enterally.

13. A method for reducing tumor size or tumor burden in a subject in need thereof, comprising administering to the subject an effective amount of a pharmaceutical composition containing a calprotectin inhibitor.

14. The method of claim 13 , further comprising administering cyclophosphamide in combination or alternation with the pharmaceutical composition.

15. A method for inhibiting or reducing breast cancer cell metastasis in a subject in need thereof comprising administering to the subject a composition comprising at least one calprotectin inhibitor, in an amount effective to inhibit or reduce cancer cell metastasis, and a pharmaceutically acceptable excipient.

Assignees

• Univ Res Inst Inc Augusta

Inventors

• Korkaya Hasan
• Lee Eunmi

Classifications

• A61K31/675 Primary

  having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate · CPC title

• A61K31/122 Primary

  having the oxygen directly attached to a ring, e.g. quinones, vitamin K1, anthralin · CPC title

• A61P35/04

  specific for metastasis · CPC title

• C07C49/84

  containing ether groups, [IMAGE cpc-sch-C07C-0958.gif] groups,[IMAGE cpc-sch-C07C-0959.gif] groups, or[IMAGE cpc-sch-C07C-0960.gif] groups · CPC title

• C07C50/34

  the quinoid structure being part of a condensed ring system having three rings · CPC title