IP Library Granted Patent US 8,859,207
Granted Patent B2
US 8,859,207 · App. 13/395,976 · Granted Oct 14, 2014

Pharmaceutical compositions which inhibit FKBP52-mediated regulation of androgen receptor function and methods of using same

Inventors: Leonard M. Neckers (Bethesda, MD); Marc B. Cox (El Paso, TX); Jane B. Neckers (Bethesda, MD); Yeong Sang Kim (Gaithersburg, MD); Aki Iwai (Toride, JP); Yangmin Ning (Silver Spring, MD); Johanny Tonos de Leon (Frederick, MD); Heather Balsiger (El Paso, TX)
Assignees: The United States of America, as represented by the Secretary, Department of Health and Human Services; University of Texas at El Paso
A61K31/192A61K31/167A61K45/06A61K31/4741A61K31/165A61K31/40A61K31/4355
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Quick Facts
Patent No.
US 8,859,207
App. No.
13/395,976
Granted
Oct 14, 2014
Kind
B2
Abstract

Pharmaceutical compositions that bind to a predicted FK506 Binding Protein 52 (FKBP52) interaction surface on the androgen receptor hormone binding domain, otherwise known as FKBP52 Targeting Agents (FTAs) are provided. These compositions of the present invention are found to specifically recognize the FKBP52 regulatory surface on the androgen receptor and inhibit FKBP52 from functionally interacting with the androgen receptor. Compositions comprising the pharmaceutical composition, as well as methods of use, treatment and screening are also provided.

Claims (9)

1. A method of identifying a compound in vitro which inhibits FKBP52-enhanced, androgen receptor (AR)-mediated activity, the method comprising:

a) providing an AR tester cell, the tester cell comprising a murine embryonic fibroblast derived from FKBP-52 deficient mice, the tester cell being transfected with a DNA encoding AR, an AR-responsive reporter plasmid, and a vector encoding a FKBP52 protein;

b) providing a control cell, the control cell comprising the murine embryonic fibroblast derived from FKBP-52 deficient mice, the control cell being transfected with the DNA encoding AR, the AR-responsive reporter plasmid, and a vector that does not encode FKBP-52;

c) contacting the cell of a) and b) with a test compound;

d) contacting the cell of a) and b) with an AR agonist;

e) incubating the cell of a) and b) for a period of time;

f) measuring an amount of AR-responsive reporter expression in a) and b); and

g) comparing the amount of AR-responsive reporter expression in the cell of a) and b),

wherein the test compound is identified as inhibiting FKBP-52-enhanced, AR-mediated activity when the amount of AR-responsive reporter expression in the cell of a) is less than the amount of AR-responsive reporter expression in the cell of b).

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE NAME PREVIOUSLY RECORDED AT REEL: 028155 FRAME: 0404. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Oct 29, 2014
From: NECKERS, LEONARD M.; COX, MARC B.; NECKERS, JANE B.; KIM, YEONG SANG; IWAI, AKI; NING, YANGMIN; TONOS DE LEON, JOHANNY; BALSIGER, HEATHER A.; FLETTERICK, ROBERT
To: THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES; BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM; THE REGENTS OF THE UNIVERSITY OF CALIFORNIA, A CALIFORNIA CORPORATION
Reel/Frame 034083/0454 →
CONFIRMATORY LICENSE Recorded Mar 26, 2013
From: UNIVERSITY OF CALIFORNIA SAN FRANCISCO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 030085/0950 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2012
From: NECKERS, LEONARD M.; COX, MARC B.; NECKERS, JANE B.; KIM, YEONG SANG; IWAI, AKI; NING, YANGMIN; TONOS DE LEON, JOHANNY; BALSIGER, HEATHER A.; FLETTERICK, ROBERT
To: THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES; UNIVERSITY OF TEXAS AT EL PASO; THE REGENTS OF THE UNIVERSITY OF CALIFORNIA, A CALIFORNIA CORPORATION
Reel/Frame 028155/0404 →
Continuity (2)
Provisional Application 61242541 · Sep 15, 2009
Related Publication 20120283215A1 · Nov 8, 2012