Description of Invention:
Niemann-Pick disease is a class of inherited lipid storage diseases. Niemann-Pick Type C disease is an autosomal recessive neurovisceral lipid storage disorder which leads to systemic and neurological abnormalities including ataxia, seizures, and loss of speech. Patients with the disease typically die as children. The biochemical hallmark of Niemann-Pick Type C cells is the abnormal accumulation of unesterified cholesterol in lysosomes, which results in the delayed homeostatic regulation of both uptake and esterification of low density lipoprotein (LDL) cholesterol. Niemann-Pick Type C is characterized by phenotypic variability. The disease appears at random in families that have no history of the disorder, making diagnosis problematic. This invention provides the human gene for Niemann-Pick Type C disease and the nucleic acid sequences corresponding to the human gene for Niemann-Pick Type C disease. Also provided is the mouse homolog of the human gene. The invention could lead to improved diagnosis and the design of therapies for the disease and improved means of detection of carriers of the gene. In addition, this invention may contribute to the understanding and development of treatments for atherosclerosis, a more common disorder associated with cholesterol buildup that involves the accumulation of fatty tissue inside arteries that blocks blood flow, leading to heart disease and stroke. The invention may also lead to additional discoveries concerning how cholesterol is processed in the body.
Inventors:
Eugene D. Carstea (NINDS) et al.
Patent Status:
DHHS Reference No. E-122-1997/0 --
U.S. Patent No. 6,426,198 issued 30 Jul 2002
U.S. Patent No. 7,045,675 issued 16 May 2006
Relevant Publication:
S.K. Loftus et al., "Murine model of Niemann-Pick C disease: Mutation in a cholesterol homeostasis gene," Science 277(5323):232-235, 1997.
S.K. Loftus et al., "Rescue of neurodegeneration in Niemann Pick-C mice by a prion-promoter driven Npc1 cDNA transgene," Human Molec. Genet. 11(24):3107-14, 2002.
Licensing Status: Licensees sought.
Also, the NHGRI Genetic Disease Research Branch is seeking statements of capability or interest from parties interested in collaborative research to further develop, evaluate or commercialize Niemann-Pick Type C disease diagnostics and therapies as well as potential applications of the Niemann-Pick Type C gene related to atherosclerosis and cholesterol processing. Please contact Claire T. Driscoll for more information (telephone: 301/594-2235; email: cdriscol@mail.nih.gov).
Portfolios: Internal Medicine Gene Based Therapies Central Nervous System
Central Nervous System -Diagnostics-In Vitro-Other Central Nervous System -Diagnostics Gene Based Therapies -Diagnostics Internal Medicine-Diagnostics
For Additional Information Please Contact: Fatima Sayyid M.H.P.M.
NIH Office of Technology Transfer
6011 Executive Blvd, Suite 325
Rockville, MD 20852-3804
Phone: (301) 435-4521
Email: sayyidf@mail.nih.gov
Fax: (301) 402-0220
