Claims for Patent: 7,927,590

Summary for Patent: 7,927,590

Title:	Compositions and methods for inhibiting growth of smad4-deficient cancers
Abstract:	The present invention is in the fields of cell biology, immunology and oncology. The invention relates to the discovery that there is a relationship between the expression levels of the tumor suppressor gene smad4 (also known as dpc4) and integrin .alpha..sub.v.beta..sub.6, and the responsiveness of patient populations to .alpha..sub.v.beta..sub.6-active compounds and compositions (e.g., antibodies and other ligands that bind .alpha..sub.v.beta..sub.6), particularly in cancer cells from such patient populations, more particularly on carcinomas such as pancreatic carcinomas. The invention thus provides methods for determining the responsiveness of tumor cells (particularly those from pancreatic tumors) to such .alpha..sub.v.beta..sub.6-active compounds and compositions by examining the expression of .alpha..sub.v.beta..sub.6 and smad4 by the tumor cells, as well as methods of diagnosis and treatment/prevention of tumor progression using ligands, including antibodies and small molecule drugs, that bind to integrin .alpha..sub.v.beta..sub.6 on the surfaces of tumor cells and/or that block one or more components of the TGF-.beta. pathway, particularly in smad4-deficient tumor cells.
Inventor(s):	Violette; Shelia M. (Lexington, MA), Koopman; Louise A. (Brookline, MA)
Assignee:	Biogen Idec MA Inc. (Cambridge, MA)
Application Number:	11/822,859
Patent Claims:	1. A method of inhibiting growth of a cell from a tumor that is smad4 deficient, comprising: (a) determining the level of expression of smad4 in a cell from said cancer; and (b) treating a cancer cell that is deficient in smad4 expression with one or more .alpha.v.beta.6 antagonist antibody that selectively binds to the integrin .alpha.v.beta.6 in said cancer cell, wherein said one or more antibody is an antibody from a hybridoma selected from the group consisting of 2A1 (deposited under ATCC Accession No. ATCC PTA-3896), 2E5 (deposited under ATCC Accession No. ATCC PTA-3897), 1A8 (deposited under ATCC Accession No. ATCC PTA-3647), 2B10 deposited under ATCC Accession No. ATCC PTA-3648), 2B1 deposited under ATCC Accession No. ATCC PTA-3646), 1G10 (deposited under ATCC Accession No. ATCC PTA-3898), 7G5 (deposited under ATCC Accession No. ATCC PTA-3899), 8G6 (deposited under ATCC Accession No. ATCC PTA-3645), 3G9 (deposited under ATCC Accession No. ATCC PTA-3649), or a humanized version thereof wherein said treatment results in the growth inhibition of said cancer cell. 2. The method of claim 1, wherein said tumor is a carcinoma. 3. The method of claim 2, wherein said carcinoma is an adenocarcinoma. 4. The method of claim 2, wherein said carcinoma is selected from the group consisting of a pancreatic carcinoma, a colorectal carcinoma, a cervical carcinoma, squamous cell carcinoma, a head and neck carcinoma, a liver carcinoma, an ovarian carcinoma and a lung carcinoma. 5. The method of claim 2, wherein said carcinoma is a pancreatic carcinoma. 6. The method of claim 4, wherein said squamous cell carcinoma is an esophageal carcinoma. 7. The method of claim 2, wherein said carcinoma is a colorectal carcinoma. 8. The method of claim 2, wherein said carcinoma is a cervical carcinoma. 9. The method of claim 2, wherein said carcinoma is a head and neck carcinoma. 10. The method of claim 1, wherein said monoclonal antibody is 3G9. 11. The method of claim 1, wherein said monoclonal antibody is 8G6. 12. The method of claim 1, wherein said monoclonal antibody is a humanized monoclonal antibody. 13. The method of claim 12, wherein said humanized monoclonal antibody is hu3G9 (BG00011). 14. The method of claim 12, wherein said humanized monoclonal antibody is hu8G6. 15. The method of claim 1, wherein said antibody is conjugated with at least one detectable label. 16. The method of claim 15, wherein said detectable label is selected from the group consisting of a chromogenic label, an enzyme label, a radioisotopic label, a non-radioactive isotopic label, a fluorescent label, a toxic label, a chemiluminescent label, an X-radiographic label, a spin label and a nuclear magnetic resonance contrast agent label. 17. The method of claim 16, wherein said chromogenic label is selected from the group consisting of diaminobenzidine and 4 hydroxyazo-benzene-2-carboxylic acid. 18. The method of claim 16, wherein said enzyme label is selected from the group consisting of malate dehydrogenase, staphylococcal nuclease, delta 5 steroid isomerase, yeast alcohol dehydrogenase, alpha glycerol phosphate dehydrogenase, triose phosphate isomerase, peroxidase, alkaline phosphatase, asparaginase, glucose oxidase, .beta. galactosidase, ribonuclease, urease, catalase, glucose 6 phosphate dehydrogenase, glucoamylase and acetylcholine esterase. 19. The method of claim 16, wherein said radioisotopic label is selected from the group consisting of 3H, 111 In, 125I, 131I, 32P, 35S, 14C, 51Cr, 57To, 58Co, 59Fe, 75Se, 152Eu, 90Y, 67Cu, 217Ci, 211At, 212Pb, 47Sc and 109Pd. 20. The method of claim 16, wherein said non-radioactive isotopic label is selected from the group consisting of 157Gd, 55Mn, 162Dy, 52Tr, 56Fe, 99mTc and 112In. 21. The method of claim 16, wherein said fluorescent label is selected from the group consisting of a 152Eu label, a fluorescein label, an isothiocyanate label, a rhodamine label, a phycoerythrin label, a phycocyanin label, an allophycocyanin label, a Green Fluorescent Protein (GFP) label, an ophthaldehyde label and a fluorescamine label. 22. The method of claim 16, wherein said toxic label is selected from the group consisting of a diphtheria toxin label, a ricin label and a cholera toxin label. 23. The method of claim 16, wherein said chemiluminescent label is selected from the group consisting of a luminol label, an isoluminol label, an aromatic acridinium ester label, an imidazole label, an acridinium salt label, an oxalate ester label, a luciferin label, a luciferase label and an aequorin label. 24. The method of claim 16, wherein said X-radiographic label is barium or cesium. 25. The method of claim 16, wherein said spin label is deuterium. 26. The method of claim 16, wherein said nuclear magnetic resonance contrast agent label is selected from the group consisting of Gd, Mn and iron. 27. A method of increasing the responsiveness of a smad4-deficient cancer cell to treatment with a growth-inhibiting chemotherapeutic compounds, comprising: (a) determining the level of expression of smad4 in a cell from said cancer; and (b) treating a cancer cell that is deficient in smad4 expression with one or more .alpha.v.beta.6-antagonist antibodies that selectively bind to the integrin .alpha.v.beta.6 in said cancer cell, wherein said one or more antibody is an antibody from a hybridoma selected from the group consisting of 2A1 (deposited under ATCC Accession No. ATCC PTA-3896), 2E5 (deposited under ATCC Accession No. ATCC PTA-3897), 1A8 (deposited under ATCC Accession No. ATCC PTA-3647), 2B10 deposited under ATCC Accession No. ATCC PTA-3648), 2B1 deposited under ATCC Accession No. ATCC PTA-3646), 1G10 (deposited under ATCC Accession No. ATCC PTA-3898), 7G5 (deposited under ATCC Accession No. ATCC PTA-3899), 8G6 (deposited under ATCC Accession No. ATCC PTA-3645), 3G9 (deposited under ATCC Accession No. ATCC PTA-3649), or a humanized version thereof wherein said treatment with said blocking antibodies results in increased responsiveness of said cancer cell to one or more growth-inhibiting chemotherapeutic compounds as compared to the growth inhibition of said cancer cell produced by said chemotherapeutic agent alone. 28. The method of claim 27, wherein said growth-inhibiting chemotherapeutic compound is selected from the group consisting of cisplatin, carboplatin, oxaliplatin, paclitaxel, gemcitabine, adriamycin, melphalan, methotrexate, 5-fluorouracil, etoposide, mechlorethamine, cyclophosphamide, bleomycin, a calicheamicin, a maytansine, a trichothene, CC1065, diphtheria A chain, Pseudomonas aeruginosa exotoxin A chain, ricin A chain, abrin A chain, modeccin A chain, alpha-sarcin, an Aleuritesfordii protein, a dianthin protein, a Phytolaca americana protein, momordica charantia inhibitor, curcin, crotin, sapaonaria officinalis inhibitor, gelonin, mitogellin, restrictocin, phenomycin, enomycin, a tricothecene, a ribonuclease, and a deoxyribonuclease. 29. The method of claim 28, wherein said growth-inhibiting chemotherapeutic compound is gemcitabine, adriamycin or paclitaxel.

Details for Patent 7,927,590

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Recordati Rare Diseases, Inc.	ELSPAR	asparaginase	For Injection	101063	01/10/1978		2026-07-10