The cell cycle hypothesis of Alzheimer's disease: Suggestions for drug development

被引:44
作者
Woods, Jack
Snape, Mike
Smith, Mark A.
机构
[1] Neuropharm Ltd, Leatherhead KT22 9HD, Surrey, England
[2] Univ Oxford, Dept Expt Psychol, Oxford OX1 3UD, England
[3] Case Western Reserve Univ, Dept Pathol, Cleveland, OH 44106 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2007年 / 1772卷 / 04期
关键词
Alzheimer's disease; cell cycle; drug development; neuroprotection;
D O I
10.1016/j.bbadis.2006.12.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cell cycle of hypothesis of neural dysfunction in chronic neurodegenerative conditions such as Alzheimer's disease (AD) offers a unified approach to understanding both existing and novel strategies for drug development. At the present time, a ligand based approach is a pragmatic solution for identifying new chemical leads on which to base future discovery and optimisation. We have pursued a ligand based approach on the basis of public domain data to identify existing compounds capable of abrogating the cell cycle at the G(0)-G(1) interface. Selected on this basis, irrespective of the tissue under study, we identified several classes of compounds as potential chemical leads. Of these compounds, at least ten have already been shown to be neuroprotective in animal models of acute neurodegeneration. Such compounds could form the basis of a screening exercise after development of suitable screening tools. Progressing of chemical leads through such an approach will be more efficient if future leads display relevant "drug-like" properties. Further, drug development in this arena should take account of the special concerns raised by targeting an elderly population. This will involve accounting for frequent polypharmacy in the aging population, and age-related alterations in physiology. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:503 / 508
页数:6
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