4.6 Review

BACE1 Physiolocical Functions May Limit Its Use as Therapeutic Tarcet for Alzneimer's Disease

期刊

TRENDS IN NEUROSCIENCES
卷 39, 期 3, 页码 158-169

出版社

ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tins.2016.01.003

关键词

-

资金

  1. European Research Council (ERC) [ERC-2010-AG_268675]
  2. Fonds voor Wetenschappelijk Onderzoek (FWO)
  3. Fonds voor Innovatie door Wetenschap en Technologie (IWT)
  4. KU Leuven
  5. VIB
  6. KU Leuven/Flemish Government (Methusalem grant)
  7. BMBF (RIModFID)
  8. Deutsche Forschungsgemeinschaft [FOR 2290]
  9. Helmholtz Israel program
  10. Bax-Vanluffelen Chair for Alzheimer's Disease
  11. 'Opening the Future' of the Leuven Universiteit Fonds (LUF)

向作者/读者索取更多资源

The protease beta-site amyloid precursor protein (APP)-cleaving enzyme 1 (BACE1) is required for the production of the amyloid-beta (A beta) peptide, which is central to the pathogenesis of Alzheimer's disease (AD). Chronic inhibition of this protease may temper amyloid production and cure or prevent AD. However, while BACE1 inhibitors are being pushed forward as drug candidates, a remarkable gap in knowledge on the physiological functions of BACE1 and its close homolog BACE2 becomes apparent. Here we discuss the major discoveries of the past 3 years concerning BACE1 biology and to what extent these could limit the use of BACE1 inhibitors in the clinic.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据