Use of APE1/Ref-1 inhibitors for treatment of retinal diseases
Combination therapies including a Apurinic/Apyrimidinic Endonuclease/reduction-oxidation (redox) Factor-1 (APE1/Ref-1) inhibitor specific to inhibit the redox function of APE1/Ref-1 are disclosed herein. The Combination therapies can be used for treating various cancers, as well as other angiogenesis-mediated diseases (e.g., retinal diseases, cardiovascular diseases).
1. A method of treating a retinal disease selected from the group consisting of choroidal neovascularization (CNV), retinopathy of prematurity (ROP), and ischemic retinopathy in a subject in need thereof, the method comprising administering to the subject a APE1/Ref-1 inhibitor, wherein the APE1/Ref-1 inhibitor is (2E)-2-[(3-methoxy-1,4-dioxo-1,4-dihydronapthalen-2-yl)methylidene]-N-methoxypentanamide] (APX2014), and wherein the APE1/Ref-1 inhibitor inhibits the redox function.
2. The method as set forth in claim 1 further comprising administering a second therapeutic agent.
3. The method as set forth in claim 2 , wherein the second therapeutic agent is selected from the group consisting of doxorubicin, endostatin, 5-fluorouracil (5-FU), bortezomib, ispinesib mesylate, SN-38, topotecan, paclitaxel, bryostatin 1, trametinib, LAQ824, vinblastine, BEZ235, panobinostat, methotrexate, temsirolimus, FK866, afatinib, tozasertib, irinotecan, GSK2126458, CPI-613, γ-secretase inhibitors, DLL4-inhibiting antibodies, and combinations thereof.
4. A method of treating a retinal disease selected from the group consisting of age-related macular degeneration (AMD) and diabetic retinopathy (DR) in a subject in need thereof, the method comprising administering to the subject a APE1/Ref-1 inhibitor, wherein the APE1/Ref-1 inhibitor is (2E)-2-[(3-methoxy-1,4-dioxo-1,4-dihydronapthalen-2-yl)methylidene]-N-methoxypentanamide] (APX2014), and wherein the APE1/Ref-1 inhibitor inhibits the redox function.
5. The method as set forth in claim 4 further comprising administering a second therapeutic agent.
6. The method as set forth in claim 5 , wherein the second therapeutic agent is selected from the group consisting of doxorubicin, endostatin, 5-fluorouracil (5-FU), bortezomib, ispinesib mesylate, SN-38, topotecan, paclitaxel, bryostatin 1, trametinib, LAQ824, vinblastine, BEZ235, panobinostat, methotrexate, temsirolimus, FK866, afatinib, tozasertib, irinotecan, GSK2126458, CPI-613, y-secretase inhibitors, DLL4-inhibiting antibodies, and combinations thereof.