SPARC binding peptides and uses thereof
The invention provides SPARC and Albumin binding peptides for the targeting of disease sites, such as tumors, with therapeutic and diagnostic agents. In particular, compositions comprising SPARC binding peptide-Antibody Fc domain fusion proteins and methods of their use are disclosed.
1. A method of treating a mammal comprising administering to the mammal a therapeutically or diagnostically effective amount of a pharmaceutical composition comprising a therapeutic or diagnostic agent coupled to a SPARC-binding-peptide (SBP) and a pharmaceutically acceptable carrier, wherein the SBP consists of any one or more of SEQ ID NOS: 1-112 or 117.
2. The method of claim 1 , wherein the therapeutic or diagnostic agent is a diagnostic agent selected from the group consisting of radioactive agents, MRI contrast agents, X-ray contrast agents, ultrasound contrast agents, and PET contrast agents.
3. The method of claim 1 , wherein the pharmaceutical composition further comprises an albumin binding peptide (ABP) consisting of SEQ ID NO: 120.
4. The method of claim 1 , wherein the mammal is a human patient.
5. The method of claim 1 , wherein the SBP consists of SEQ ID NO: 1.
6. The method of claim 1 , wherein the SBP consists of SEQ ID NO: 2.
7. The method of claim 1 , wherein the therapeutic or diagnostic agent is a therapeutic agent selected from the group consisting of platinum compounds, antifolates, antimetabolites, antimitotics, DNA damaging agents, proapoptotics, differentiation inducing agents, antiangiogenic agents, antibiotics, tyrosine kinase inhibitors, kinase inhibitors, biologically active agents, biological molecules, hormones, peptides, antibodies, antibodies fragments and combinations thereof.
8. The method of claim 7 , wherein the therapeutic agent is selected from the group consisting of radionuclides, adriamycin, ansamycin antibiotics, asparaginase, bleomycin, busulphan, cisplatin, carboplatin, carmustine, capecitabine, chlorambucil, cytarabine, cyclophosphamide, camptothecin, dacarbazine, dactinomycin, daunorubicin, dexrazoxane, docetaxel, doxorubicin, etoposide, epothilones, floxuridine, fludarabine, fluorouracil, gemcitabine, hydroxyurea, idarubicin, ifosfamide, irinotecan, lomustine, mechlorethamine, mercaptopurine, meplhalan, methotrexate, rapamycin (sirolimus), mitomycin, mitotane, mitoxantrone, nitrosurea, paclitaxel, pamidronate, pentostatin, plicamycin, procarbazine, rituximab, streptozocin, teniposide, thioguanine, thiotepa, taxanes, vinblastine, vincristine, vinorelbine, taxol, combretastatins, discodermolides, transplatinum, docetaxel, paclitaxel, taxanes, 5-fluorouracil, genistein, tTF, TNF, Smar1 derived p44 peptide, interferon, TRAIL, Smac, VHL, procaspase, caspase, and IL-2, a non-Fc domain antibody fragment, and combinations thereof.
9. The method of claim 7 , wherein the therapeutic agent is an antibody fragment comprising a functional antibody Fc domain.
10. The method of claim 9 , wherein the therapeutic agent is an antibody fragment which mediates one or more of complement activation, cell mediated cytotoxicity, inducing apoptosis, inducing cell death, and opsinization.
11. The method of claim 9 , wherein the functional antibody Fc domain comprises SEQ ID NO: 118.