Claims for Patent: 7,838,531

Summary for Patent: 7,838,531

Title:	Farnesyltransferase inhibitors for treatment of laminopathies, cellular aging and atherosclerosis
Abstract:	Although it can be farnesylated, the mutant lamin A protein expressed in Hutchison Gilford Progeria Syndrome (HGPS) cannot be defarnesylated because the characteristic mutation causes deletion of a cleavage site necessary for binding the protease ZMPSTE24 and effecting defarnesylation. The result is an aberrant farnesylated protein (called "progerin") that alters normal lamin A function as a dominant negative, as well as assuming its own aberrant function through its association with the nuclear membrane. The retention of farnesylation, and potentially other abnormal properties of progerin and other abnormal lamin gene protein products, produces disease. Farnesyltransferase inhibitors (FTIs) (both direct effectors and indirect inhibitors) will inhibit the formation of progerin, cause a decrease in lamin A protein, and/or an increase prelamin A protein. Decreasing the amount of aberrant protein improves cellular effects caused by and progerin expression. Similarly, treatment with FTIs should improve disease status in progeria and other laminopathies. In addition, elements of atherosclerosis and aging in non-laminopathy individuals will improve after treatment with farnesyltransferase inhibitors.
Inventor(s):	Gordon; Leslie B. (Foxboro, MA), Collins; Francis S. (Rockville, MD), Glover; Thomas (Ypsilanti, MI), Glynn; Michael W. (Darien, CT), Capell; Brian C. (Rumson, NJ), Cox; Adrienne D. (Chapel Hill, NC), Der; Channing J. (Chapel Hill, NC)
Assignee:	The United States of America as represented by the Department of Health and Human Services (Washington, DC) N/A (Anne Arbor, MI) The Regents of the University of Michiga (Peabody, MA) Progeria Research Foundation, Inc. (Chapel Hill, NC) The University of North Carolina at Chapel Hill (N/A)
Application Number:	11/828,117
Patent Claims:	1. A method of reducing at least one cellular defect in a cell from a subject having a disease or condition selected from the group consisting of Hutchinson-Gilford Progeria Syndrome, progeria, Emery-Dreifuss muscular dystrophy, Limb-Girdle muscular dystrophy, Charcot-Marie-Tooth disorder, Werner syndrome, and dilated cardiomyopathy with conduction system disease, wherein the cellular defect is one or more cellular defects selected from the group consisting of mis-localization of a farnesylated lamin, mis-localization of a non-farnesylated lamin, nuclear membrane disruption, aggregation of lamin, nuclear lobulation, nuclear blebbing, cytoskeleton disruption, early senescence, premature apoptosis, and reduced secretion of MMP-3; the method comprising administering to the cell a therapeutically effective dose of a farnesyltransferase inhibitor (FTI). 2. The method of claim 1, wherein the disease or condition is characterized by farnesylation of an abnormally farnesylated lamin or normally non-farnesylated lamin. 3. The method of claim 2, wherein the abnormally farnesylated lamin or normally non-farnesylated lamin is a lamin other than lamin B. 4. The method of claim 3, wherein the lamin other than lamin B is lamin A. 5. The method of claim 1, wherein the FTI is PD169541, R115777, SCH66336, L-744832 or FTI-2153. 6. A method of reducing at least one cellular defect in a subject having or predisposed to a disease or condition selected from the group consisting of Hutchinson-Gilford Progeria Syndrome, progeria, Emery-Dreifuss muscular dystrophy, Limb-Girdle muscular dystrophy, Charcot-Marie-Tooth disorder, Werner syndrome disease, and dilated cardiomyopathy with conduction system disease, wherein the cellular defect is one or more cellular defects selected from the group consisting of mis-localization of a farnesylated lamin, mis-localization of a non-farnesylated lamin, nuclear membrane disruption, aggregation of lamin, nuclear lobulation, nuclear blebbing, cytoskeleton disruption, early senescence, premature apoptosis, and reduced secretion of MMP-3; the method comprising administering to the subject a therapeutically effective dose of a farnesyltransferase inhibitor (FTI). 7. The method of claim 6, wherein the progeroid disease or condition is characterized by farnesylation of an abnormally farnesylated lamin or normally non-farnesylated lamin. 8. The method of claim 7, wherein the abnormally farnesylated lamin or normally non-farnesylated lamin is a lamin other than lamin B. 9. The method of claim 8, wherein the lamin other than lamin B is lamin A. 10. The method of claim 6, wherein the FTI is PD169541, R115777, SCH66336, L-744832 or FTI-2153. 11. The method of claim 6, wherein the method treats the subject having or predisposed to the disease or condition.