IP Library Granted Patent US 7,217,795
Granted Patent B2
US 7,217,795 · App. 10/299,003 · Granted May 15, 2007

Tumor suppressor designated TS10q23.3

Assignees: Myriad Genetics, Inc.; Board of Regents, The University of Texas Systems
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Quick Facts
Patent No.
US 7,217,795
App. No.
10/299,003
Granted
May 15, 2007
Kind
B2
Abstract

A specific region of chromosome 10 (10q23.3) has been implicated by series of studies to contain a tumor suppressor gene involved in gliomas, as well as a number of other human cancers. One gene within this region was identified, and the corresponding coding region of the gene represents a novel 47 kD protein. A domain of this product has an exact match to the conserved catalytic domain of protein tyrosine phosphatases, indicating a possible functional role in phosphorylation events. Sequence analyses demonstrated the a number of exons of the gene were deleted in tumor cell lines used to define the 10q23.3 region, leading to the classification of this gene as a tumor suppressor. Further analyses have demonstrated the presence of a number of mutations in the gene in both glioma and prostate carcinoma cells. Methods for diagnosing and treating cancers related to this tumor suppressor, designated as TS10q23.3, also are disclosed.

Claims (28)

1. An isolated antibody that binds immunologically to a protein, wherein the amino acid sequence of said protein consists of the amino acid sequence set forth in SEQ ID NO:2.

2. The antibody of claim 1 , wherein the antibody is a monoclonal antibody.

3. The antibody of claim 1 , wherein the antibody is a polyclonal antibody.

4. The monoclonal antibody of claim 2 , wherein the antibody further comprises a detectable label.

5. The antibody of claim 1 , wherein said antibody binds immunologically with recombinant SEQ ID NO:2.

6. The antibody of claim 5 , wherein said antibody is a monoclonal antibody.

7. A method of producing an antibody an comprising:

(a) immunizing a suitable animal with a composition comprising a an immunogen;

(b) isolating B-lympocytes from said animal;

(c) fusing said B-lymphocytes with an immortal myeloma cell to yield a hybridoma;

(d) selecting a hybridoma producing an antibody that binds immunologically to an immunogen, wherein the amino acid seciuence of said immunogen consists of the amino acid sequence set forth in SEQ ID NO:2, thereby producing said antibody.

8. The method of claim 7 , wherein the immunogen is selected from the group consisting of purified protein, partially purified protein recombinant protein, wherein the amino acid sequence of said protein consists of the amino acid sequence set forth in SEQ ID NO:2.

9. The method of claim 7 , wherein said composition comprising a said immunogen further comprises an adjuvant.

10. The method of claims 8 , wherein said immunogen is recombinant SEQ ID NO:2.

11. A hybridoma capable of producing an antibody that binds immunologically to a protein, wherein the amino acid sequence of said protein consists of the amino acid sequence set forth in SEQ ID NO:2.

12. The hybridoma of claim 11 wherein said hybridoma is produced from the fusion of a murine B-lymphocyte and a murine immortal myeloma cell.

13. An isolated antibody specifically immunoreactive with a protein wherein the amino acid sequence of said protein consists of the amino acid sequence set forth in SEQ ID NO:2.

14. The antibody of claim 13 , wherein the antibody is a monoclonal antibody.

15. The antibody of claim 13 , wherein the antibody is a polyclonal antibody.

16. The monoclonal antibody of claim 13 , wherein the antibody further comprises a detectable label.

17. The antibody of claim 13 , wherein said antibody binds immunologically with recombinant SEQ ID NO:2.

18. The antibody of claim 13 , wherein said antibody is a monoclonal antibody.

19. The monoclonal antibody of claim 2 , wherein said antibody is not cross reactive with other human polypeptides.

20. The monoclonal antibody of claim 14 , wherein said antibody is not cross reactive with other human polypeptides.

21. The antibody of claim 1 , wherein said antibody is a humanized antibody.

22. The antibody of claim 13 , wherein said antibody is a humanized antibody.

23. A composition comprising the antibody of claim 1 .

24. A composition comprising the antibody of claim 13 .

Assignments (5)
CONFIRMATORY LICENSE Recorded May 23, 2018
From: MD ANDERSON CANCER CENTER
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 045878/0956 →
CONFIRMATORY LICENSE Recorded May 31, 2012
From: UNIVERSITY OF TEXAS M. D. ANDERSON CANCER CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 028306/0326 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 23, 2009
From: MYRIAD GENETICS, INC.
To: BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 022990/0662 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 25, 2006
From: TAVTIGIAN, SEAN V.
To: MYRIAD GENETICS, INC.
Reel/Frame 018309/0707 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 25, 2006
From: STECK, PETER; PERSHOUSE, MARK A.; JASSER, SAMAR; YUNG, W.K. ALFRED
To: BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 018309/0710 →
Continuity (5)
Division 0914074900 · Aug 26, 1998
Continuation In Part 0879111500 · Jan 30, 1997
Provisional Application 6008356300 · Apr 30, 1998
Provisional Application 6005775000 · Aug 26, 1997
Related Publication 20030139324A1 · Jul 24, 2003