IP Library › Granted Patent US 7,947,276
Granted Patent B2
US 7,947,276 · App. 11/584,413 · Granted May 24, 2011

Antibodies and molecules derived therefrom that bind to STEAP-1 proteins

Assignee: Agensys, Inc.
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Quick Facts
Patent No.
US 7,947,276
App. No.
11/584,413
Granted
May 24, 2011
Kind
B2
Abstract

Antibodies and molecules derived therefrom that bind to novel STEAP-1 protein, and variants thereof, are described wherein STEAP-1 exhibits tissue specific expression in normal adult tissue, and is aberrantly expressed in the cancers listed in Table I. Consequently, STEAP-1 provides a diagnostic, prognostic, prophylactic and/or therapeutic target for cancer. The STEAP-1 gene or fragment thereof, or its encoded protein, or variants thereof, or a fragment thereof, can be used to elicit a humoral or cellular immune response; antibodies or T cells reactive with STEAP-1 can be used in active or passive immunization.

Claims (15)

1. A method of delivering a calcium channel inhibitor to a cell that expresses STEAP-1 protein (SEQ ID NO:3), comprising:

providing a calcium channel inhibitor conjugated to an antibody or fragment thereof comprising an antigen binding site that binds specifically to STEAP-1 protein (SEQ ID NO:3), to form an antibody-inhibitor or fragment-inhibitor conjugate; and

exposing the cell to the antibody-inhibitor or fragment-inhibitor conjugate.

2. The method of claim 1 wherein the calcium channel inhibitor is selected from the group consisting of amlodipine, azulene, dihydropyridines, thianines, nifedine, verapamil, nordihydroguaiaretic acid (NDGA), and derivatives thereof.

3. A method of inhibiting the growth of a cancer cell that expresses STEAP-1 protein (SEQ ID NO:3), comprising:

providing a calcium channel inhibitor conjugated to an antibody or fragment thereof comprising an antigen binding site that binds specifically to STEAP-1 protein (SEQ ID NO:3), to form an antibody-inhibitor or fragment-inhibitor conjugate; and

exposing the cell to the antibody-inhibitor or fragment-inhibitor conjugate.

4. The method of claim 3 wherein the calcium channel inhibitor is selected from the group consisting of amlodipine, azulene, dihydropyridines, thianines, nifedine, verapamil, nordihydroguaiaretic acid (NDGA), and derivatives thereof.

5. The method of claim 3 wherein the cancer is metastatic.

6. The method of claim 3 wherein the cancer is prostate, bladder, kidney, colon, lung, pancreatic, ovary, breast, stomach or rectal cancer, or lymphoma.

7. The method of claim 3 wherein the cancer is prostate cancer.

8. A method of inhibiting the activity of STEAP-1 protein (SEQ ID NO:3), comprising:

providing a calcium channel inhibitor conjugated to antibody or fragment thereof comprising an antigen binding site that binds specifically to STEAP-1 protein (SEQ ID NO:3), to form an antibody-inhibitor or fragment-inhibitor conjugate; and

exposing the cell to the antibody-inhibitor or fragment-inhibitor conjugate.

9. The method of claim 8 wherein the calcium channel inhibitor is selected from the group consisting of amlodipine, azulene, dihydropyridines, thianines, nifedine, verapamil, nordihydroguaiaretic acid (NDGA), and derivatives thereof.

Continuity (7)
Continuation 10830899 · Apr 23, 2004
Continuation In Part 10236878 · Sep 6, 2002
Provisional Application 60370387 · Apr 5, 2002
Provisional Application 60317840 · Sep 6, 2001
Provisional Application 60087520 · Jun 1, 1998
Provisional Application 60091183 · Jun 30, 1998
Related Publication 20070160530A1 · Jul 12, 2007