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Abstract
Annual Review of Pharmacology and Toxicology
Vol. 43: 545-584 (Volume publication date April 2003)
(doi:10.1146/annurev.pharmtox.43.100901.140248)
First published online as a Review in Advance on October 4, 2002
ALZHEIMER'S DISEASE: Molecular Understanding Predicts Amyloid-Based Therapeutics

Dennis J. Selkoe1 and Dale Schenk2
1Harvard Medical School and Brigham and Women's Hospital, Boston, Massachusetts 02115; email:
2Elan Pharmaceuticals, South San Francisco, California 94080

Abstract Degenerative diseases of the brain were long considered among the most obscure and intractable of human maladies. However, recent advances in understanding their mechanisms have brought us to the verge of potential disease-modifying agents. This progress is perhaps best exemplified by the case of Alzheimer's disease. The application of molecular pathology and genetics has led to the recognition that the four genes implicated to date in familial Alzheimer's disease all chronically elevate cerebral levels of the amyloid β-protein (Aβ). Accordingly, small molecule inhibitors of the β- and γ-secretases, the proteases that generate Aβ from its precursor, are under active development, and some have shown in vivo efficacy in mouse models. An alternative approach, active or passive immunization against Aβ, has received extensive pre-clinical validation in mice, but an effective preparation free of significant side effects in humans is still awaited. Several other potential therapies are also reviewed here. If one or more of these varied approaches is ultimately proven to slow or prevent dementia, Alzheimer's disease will become a salient example of the successful application of reductionist biology to the most complex of organs, the human cerebral cortex.

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Authors:
Dennis J. Selkoe
Dale Schenk
Keywords:
amyloid β-protein
secretases
protease inhibitors
immunization
monoclonal antibodies

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