Potential repurposing of oncology drugs for the treatment of Alzheimer's disease

被引:14
|
作者
Araki, Wataru [1 ]
机构
[1] Natl Ctr Neurol & Psychiat, Natl Inst Neurosci, Dept Demyelinating Dis & Aging, Kodaira, Tokyo 1878502, Japan
来源
BMC MEDICINE | 2013年 / 11卷
关键词
Alzheimer's disease; amyloid beta-peptide; disease-modifying drugs; drug repositioning; A-BETA; THERAPEUTICS; CANCER;
D O I
10.1186/1741-7015-11-82
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Alzheimer's disease (AD) is the most common form of neurodegenerative dementia, affecting about 30 million people worldwide. Despite recent advances in understanding its molecular pathology, no mechanism-based drugs are currently available that can halt the progression of AD. Because amyloid-beta-peptide (A beta), a primary component of senile plaques, is thought to be a central pathogenic culprit, several disease-modifying therapies are being developed, including inhibitors of A beta-producing proteases and immunotherapies with anti-A beta antibodies. Drug repositioning or repurposing is regarded as a complementary and reasonable approach to identify new drug candidates for AD. This commentary will discuss the clinical relevance of an attractive candidate compound reported in a recent paper by Hayes et al. (BMC Medicine 2013) as well as perspectives regarding the possible repositioning of oncology drugs for the treatment of AD. See related research article here http://www.biomedcentral.com/1741-7015/11/81
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页数:3
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