IP Library Granted Patent US 8,859,503
Granted Patent B2
US 8,859,503 · App. 12/332,183 · Granted Oct 14, 2014

Methods and compositions targeting viral and cellular ITAM motifs, and use of same in identifying compounds with therapeutic activity

Inventors: John G Monroe (Philadelphia, PA); Elad Katz (Manchester, GB); Ramachandran Murali (Swarthmore, PA)
Assignee: The Trustees of the University of Pennsylvania
A61K38/1709
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Quick Facts
Patent No.
US 8,859,503
App. No.
12/332,183
Granted
Oct 14, 2014
Kind
B2
Abstract

This invention provides methods of treating, reducing the incidence of, and inhibiting metastasis formation of carcinomas, sarcomas, Epstein-Barr virus-induced malignancies, B cell proliferative disorders, and mast cell activation disorders, comprising administering to a subject a compound that inhibits an interaction of a first protein and an immunoreceptor tyrosine-based activation motif (ITAM) of a second protein, and screening methods for identifying ITAM-inhibitory compounds and peptides. This invention also provides peptides that inhibit signaling by ITAMs.

Claims (11)

1. A method of inhibiting metastasis of a virally-induced cancer containing proteins with immunoreceptor tyrosine based activation motifs (ITAM) or a cancer containing proteins with immunoreceptor tyrosine based activation motifs (ITAM) in a subject, comprising administering to said subject a compound that inhibits an interaction of a first protein and an immunoreceptor tyrosine-based activation motif (ITAM) of a second protein, wherein said compound comprises a peptide containing a sequence selected from the group consisting of SEQ ID NOs: 1-5, 28, 33-35 and 39.

2. The method of claim 1 , whereby the peptide is modified via hydroxylation, amidation, esterification, formylation, gamma-carboxyglutamic acid hydroxylation, methylation, phosphorylation, sulfation, glycosylation, reduction, oxidation, disulfide modification, introduction of a thioether bond, introduction of a thiolester bond, a backbone condensation, biotinylation or a combination thereof.

3. The method of claim 1 , whereby the peptide comprises an amino acid which is a D amino acid; pyrrolidone carboxylic acid; 2-aminoadipic acid; 3-aminoadipic acid; beta-alanine; beta-aminoproprionic acid; 2-aminobutyric acid; 4-aminobutyric acid; piperidinic acid; 6-aminocaproic acid; 6-aminoheptanoic acid; 2-aminoheptanoic acid; 2-aminoisobutyric acid; 3-aminoisobutyric acid; 2-aminopimelic acid; 2,4 diaminobutyric acid; desmosine; 2,2 diaminopimelic acid; 2,3 diaminopropionic acid; N-ethylglycine; N-ethylasparagine; hydroxylysine; allo-hydroxylysine; 3-hydroxyproline; 4-hydroxyproline; isodesmosine; allo-isoleucine; N-methylglycine; sarcosine; methylisoleucine; methyllysine; methylvaline; norvaline; norleucine; 6-aminohexanoic acid; citrulline; cysteic acid; cyclohexylalanine; alpha-amino isobutyric acid; t-butylglycine; t-butylalanine; phenylglycine; an N-alpha-methyl amino acid, a C-alpha-methyl amino acid, a beta-methyl amino acid, orthinine, or a combination thereof.

4. The method of claim 1 , whereby the second protein is a viral protein.

5. The method of claim 1 , whereby the metastatic virally induced cancer is a sarcoma.

6. A method of treating B cell proliferative disorder, or a mast cell activation disorder is a subject, comprising administering to said subject a compound that inhibits an interaction of a first protein and an immunoreceptor tyrosine-based activation motif (ITAM) of a second protein, wherein said compound comprises a peptide containing a sequence selected from the group consisting of SEQ ID NOs: 1-5, 28, 33-35 and 39.

7. The method of claim 6 , whereby the peptide is modified via hydroxylation, amidation, esterification, formylation, gamma-carboxyglutamic acid hydroxylation, methylation, phosphorylation, sulfation, glycosylation, reduction, oxidation, disulfide modification, introduction of a thioether bond, introduction of a thiolester bond, a backbone condensation, biotinylation or a combination thereof.

8. The method of claim 6 , whereby the peptide comprises an amino acid which is a D amino acid; pyrrolidone carboxylic acid; 2-aminoadipic acid; 3-aminoadipic acid; beta-alanine; beta-aminoproprionic acid; 2-aminobutyric acid; 4-aminobutyric acid; piperidinic acid; 6-aminocaproic acid; 6-aminoheptanoic acid; 2-aminoheptanoic acid; 2-aminoisobutyric acid; 3-aminoisobutyric acid; 2-aminopimelic acid; 2,4 diaminobutyric acid; desmosine; 2,2 diaminopimelic acid; 2,3 diaminopropionic acid; N-ethylglycine; N-ethylasparagine; hydroxylysine; allo-hydroxylysine; 3-hydroxyproline; 4-hydroxyproline; isodesmosine; allo-isoleucine; N-methylglycine; sarcosine; methylisoleucine; methyllysine; methylvaline; norvaline; norleucine; 6-aminohexanoic acid; citrulline; cysteic acid; cyclohexylalanine; alpha-amino isobutyric acid; t-butylglycine; t-butylalanine; phenylglycine; an N-alpha-methyl amino acid, a C-alpha-methyl amino acid, a beta-methyl amino acid, orthinine, or a combination thereof.

9. The method of claim 6 , whereby the second protein is a viral protein.

10. The method of claim 1 , wherein said compound consists of a peptide selected from the group consisting of SEQ ID No: 1-5, 28, 33-35 and 39.

11. The method of claim 6 , wherein said compound consists of a peptide selected from the group consisting of SEQ ID No: 1-5, 28, 33-35 and 39.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jan 20, 2010
From: UNIVERSITY OF PENNSYLVANIA
To: US ARMY, SECRETARY OF THE ARMY
Reel/Frame 023816/0682 →
EXECUTIVE ORDER 9424, CONFIRMATORY LICENSE Recorded Feb 2, 2009
From: UNIVERSITY OF PENNSYLVANIA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 022189/0617 →
Continuity (4)
Continuation 11332472 · Jan 17, 2006
Provisional Application 60643906 · Jan 14, 2005
Provisional Application 60649900 · Feb 4, 2005
Related Publication 20090258032A1 · Oct 15, 2009