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PMID: 16472155 Published · ppublish English Journal Article Review

gamma-secretase as a therapeutic target for treatment of Alzheimer's disease.

Current pharmaceutical design ·Vol. 12 ·No. 6 ·2006-00-00 ·Pages 661-70

Tomita T, Iwatsubo T

Abstract

Alzheimer's disease (AD) is the most common cause of dementia with aging, that is pathologically characterized by senile plaques that contain amyloid-beta peptides (Abeta) and neurofibrillary tangles comprised of phosphorylated tau. Genetic and biological studies provide evidence that the production and deposition of Abeta contribute to the etiology of AD. gamma-Secretase is the pivotal enzyme in generating the C terminus of Abeta, that determines its aggregability and propensity for deposition. Drugs that regulate the production of Abeta by inhibiting gamma-secretase activity could provide an effective therapeutics for AD, although recent studies suggest that gamma-secretase plays important roles in novel signaling pathways that play essential roles in embryonic development. This review focuses on recent progresses in the gamma-secretase biology that shed substantial light on the proteolytic mechanism, regulation and composition of this unusual enzyme. Moreover, we review the recent development of inhibitors and provide a direction for the effective treatment of AD through inhibition of gamma-secretase activity.

MeSH Terms
Alzheimer Disease/drug therapy,metabolism Amyloid Precursor Protein Secretases Amyloid beta-Protein Precursor/metabolism Animals Aspartic Acid Endopeptidases Endopeptidases/metabolism Enzyme Inhibitors/chemistry,therapeutic use Humans Models, Biological Molecular Structure
Chemicals
Amyloid beta-Protein Precursor Enzyme Inhibitors Amyloid Precursor Protein Secretases Endopeptidases Aspartic Acid Endopeptidases BACE1 protein, human
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tomita Taisuke
Department of Neuropathology and Neuroscience, Graduate School of Pharmaceutical Sciences, University of Tokyo, Bunkyo-ku, Japan. taisuke@mol.f.u-tokyo.ac.jp
Iwatsubo Takeshi
Article Info
Journal
Current pharmaceutical design
Abbr.
Curr Pharm Des
ISSN
1381-6128
Published
2006-00-00
Pages
661-70
Language
English
Region
United Arab Emirates
NLM ID
9602487
Subset
IM
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