Claims for Patent: 8,828,356

Summary for Patent: 8,828,356

Title:	Farnesyltransferase inhibitors for treatment of laminopathies, cellular aging and atherosclerosis
Abstract:	Although it can be farnesylated, the mutant lamin A protein expressed in Hutchinson 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. (Philadelphia, PA), Cox; Adrienne D. (Chapel Hill, NC), Der; Channing J. (Chapel Hill, NC)
Assignee:	Progeria Research Foundation, Inc. (Peabody, MA) The United States of America as represented by the Secretary of the Department of Health and Human Services (Washington, DC) N/A (Chapel Hill, NC) The University of North Carolina at Chapel Hill (Ann Arbor, MI) The Regents of the University of Michigan (N/A)
Application Number:	13/857,052
Patent Claims:	1. A method of reducing at least one clinical symptom of Hutchinson-Guilford Progeria Syndrome (HGPS) in a subject having HGPS, the method comprising administering to the subject a therapeutically effective dose of a farnesyltransferase inhibitor (FTI). 2. The method of claim 1, wherein the clinical symptom of HGPS comprises one or more of failure to thrive, maldevelopment, cardiovascular disease, abnormal bone density, distal bone resorption, osteoporosis, or decreased adipose tissue. 3. The method of claim 2, wherein the clinical symptom is a cardiovascular disease comprising one or more of atherosclerosis, atherosclerotic plaques in large or small arteries, interstitial fibrosis, stenosis, or paucity of medial smooth muscle cells. 4. The method of claim 1, wherein the method prevents progression or retards progression of HGPS in the subject. 5. The method of claim 1, wherein the FTI is PD169541, R115777, SCH66336, L-744832, FTI-2153 or a derivative thereof that maintains farnesyltransferase inhibitory activity. 6. The method of claim 1, further comprising administering a second therapeutic compound to the subject. 7. The method of claim 6, wherein the second therapeutic compound is not a farnesyltransferase inhibitor (FTI). 8. The method of claim 1, wherein the therapeutically effective amount of the FTI is about 0.1 nM per kilogram (kg) body weight to about 1 .mu.M per kg body weight. 9. The method of claim 1, wherein the therapeutically effective amount of the FTI is 0.1 to 200 mg/kg body weight. 10. The method of claim 9, wherein the therapeutically effective amount of the FTI is 1.0, 10, 25, 50, or 100 mg/kg body weight. 11. The method of claim 1, wherein the FTI is lonafarnib (SCH66336). 12. The method of claim 11, wherein the therapeutically effective amount of SCH66336 is at least 115 mg/m.sup.2 BID. 13. The method of claim 1, wherein the therapeutically effective amount of the FTI is about 1 nM to about 500 nM per kg body weight. 14. The method of claim 1, wherein the therapeutically effective amount of the FTI is about 5 nM to about 50 nM per kg body weight.