IP Library Granted Patent US 8,945,556
Granted Patent B2
US 8,945,556 · App. 13/300,063 · Granted Feb 3, 2015

RAF gene fusions

Inventors: Arul Chinnaiyan (Plymouth, MI); Nallasivam Palanisamy (Ann Arbor, MI); Shanker Kalyana-Sundaram (Ann Arbor, MI)
Assignee: The Regents of The University of Michigan
C12Q1/6886
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Quick Facts
Patent No.
US 8,945,556
App. No.
13/300,063
Granted
Feb 3, 2015
Kind
B2
Abstract

The present disclosure relates to compositions and methods for cancer diagnosis, research and therapy, including but not limited to, cancer markers. In particular, the present disclosure relates to RAF gene fusions as diagnostic markers and clinical targets for cancer.

Claims (13)

1. A composition comprising at least one of the following:

(a) an oligonucleotide probe that hybridizes to a junction of a chimeric genomic DNA or a chimeric mRNA, wherein a 5′ portion of the chimeric genomic DNA or the chimeric mRNA is from an AGTRAP gene and a 3′ portion of the chimeric genomic DNA or the chimeric mRNA is from a RAF family member gene;

(b) an antibody specific for a fusion protein having an amino-terminal portion encoded by an angiotensin II, type I receptor-associated protein (AGTRAP) gene and a carboxy-terminal portion encoded by a kinase domain of a RAF family member gene.

2. The composition of claim 1 wherein the RAF family member gene is BRAF.

3. The composition of claim 1 wherein the carboxy-terminal portion of the fusion protein comprises a wild-type sequence of a RAF family member gene.

4. The composition of claim 1 further comprising the fusion protein having an amino-terminal portion encoded by an AGTRAP gene and a carboxy-terminal portion encoded by a kinase domain of a RAF family member gene.

5. The composition of claim 1 wherein the fusion protein having an amino-terminal portion encoded by an AGTRAP gene and a carboxy-terminal portion encoded by a RAF family member gene differs from the native AGTRAP protein or the native RAF family member gene in amino acid sequence; post-translational processing; and/or secondary, tertiary, or quaternary structure.

6. The composition of claim 1 wherein the antibody is labeled.

7. The composition of claim 1 wherein the antibody is polyclonal, monoclonal, chimeric, humanized, single chain, a Fv fragment, or a Fab fragment.

8. The composition of claim 1 wherein the antibody is linked to a bead.

9. The composition of claim 1 wherein the fusion protein comprises exon 5 of AGTRAP.

10. The composition of claim 1 wherein the fusion protein comprises exon 8 of BRAF.

11. The composition of claim 1 wherein the fusion protein comprises exon 8 of BRAF fused to exon 5 of AGTRAP.

Assignments (5)
CONFIRMATORY LICENSE Recorded Jan 31, 2012
From: UNIVERSITY OF MICHIGAN
To: US ARMY, SECRETARY OF THE ARMY
Reel/Frame 027622/0924 →
CONFIRMATORY LICENSE Recorded Jan 6, 2012
From: UNIVERSITY OF MICHIGAN
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 027490/0558 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 4, 2012
From: HOWARD HUGHES MEDICAL INSTITUTE ("HHMI")
To: THE REGENTS OF THE UNIVERSITY OF MICHIGAN
Reel/Frame 027475/0015 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2011
From: CHINNAIYAN, ARUL
To: HOWARD HUGHES MEDICAL INSTITUTE ("HHMI")
Reel/Frame 027466/0563 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2011
From: PALANISAMY, NALLASIVAM; KALYANA-SUNDARAM, SHANKER
To: THE REGENTS OF THE UNIVERSITY OF MICHIGAN
Reel/Frame 027466/0578 →
Continuity (2)
Provisional Application 61415495 · Nov 19, 2010
Related Publication 20120142549A1 · Jun 7, 2012