| Literature DB >> 12212798 |
Jack T Rogers1, 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.
Abstract
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 involved 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 A beta peptide output for Alzheimer's disease therapeutics.Entities:
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Year: 2002 PMID: 12212798 DOI: 10.1007/s12031-002-0014-6
Source DB: PubMed Journal: J Mol Neurosci ISSN: 0895-8696 Impact factor: 3.444