Therapeutic strategies for human amyloid diseases

被引:224
作者
Sacchettini, JC
Kelly, JW
机构
[1] Texas A&M Univ, Dept Biochem & Biophys, College Stn, TX 77843 USA
[2] Scripps Res Inst, Dept Chem, La Jolla, CA 92075 USA
[3] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92075 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nrd769
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Amyloid diseases are a large group of a much larger family of misfolding diseases. This group includes pathologies as diverse as Alzheimer's disease, immunoglobulin-light-chain disease, reactive amyloid disease and the familial amyloid polyneuropathies. These diseases are generally incurable at present, although some drugs are known to transiently slow the progression of Alzheimer's disease. As we increase our understanding of the causative mechanisms of these disorders, the likelihood of success for a given therapeutic strategy will become clearer. This review will look at small-molecule and macromolecular approaches for intervention in amyloid diseases other than Alzheimer's disease, although select examples from Alzheimer's disease will be discussed.
引用
收藏
页码:267 / 275
页数:9
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