Alzheimer’s disease drug discovery targeted to the APP mRNA 5′Untranslated region

被引:1
|
作者
Jack T. Rogers
Jeffrey D. Randall
Paul S. Eder
Xudong Huang
Ashley I. Bush
Rudolph E. Tanzi
Amanda Venti
Sandra M. Payton
Tony Giordano
Seiichi Nagano
Catherine M. Cahill
Robert Moir
Debomoy K. Lahiri
Nigel Greig
Satinder Singh Sarang
Steven R. Gullans
机构
[1] Brigham and Women’s Hospital,Renal Division
[2] Harvard Medical School,Drug Design and Development
[3] Message Pharmaceuticals,Diabetes Research Unit
[4] National Institute on Aging,Institute of Psychiatric Research
[5] Massachusetts General Hospital,Department of Psychiatry
[6] Harvard Medical School,Neuroscience, Genetics and Aging Unit
[7] Indiana University School of Medicine,undefined
[8] Harvard Medical School,undefined
[9] Center for Neuroscience,undefined
[10] Mass General (East),undefined
来源
关键词
Alzheimer’s disease; APP mRNA 5′untranslated region; RNA-targeting; FDA-2000 Drug library; drug screen; translation;
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学科分类号
摘要
We performed a screen for drugs that specifically interact with the 5′ untranslated region of the mRNA coding for the Alzheimer’s Amyloid Precursor Protein (APP). Using a transfection based assay, in which APP 5′UTR sequences drive the translation of a downstream luciferase reporter gene, we have been screening for new therapeutic compounds that already have FDA approval and are pharmacologically and clinically well-characterized. Several classes of FDA-pre-approved drugs (16 hits) reduced APP 5′UTR-directed luciferase expression (>95% inhibition of translation). The classes of drugs include known blockers of receptor ligand interactions, bacterial antibiotics, drugs involed in lipid metabolism, and metal chelators. These APP 5′UTR directed drugs exemplify a new strategy to identify RNA-directed agents to lower APP translation and Aβ peptide output for Alzheimer’s disease therapeutics.
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页码:77 / 82
页数:5
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