| Literature DB >> 28356511 |
Tania F Gendron1,2, Jeannie Chew1,2, Jeannette N Stankowski1, Lindsey R Hayes3, Yong-Jie Zhang1,2, Mercedes Prudencio1,2, Yari Carlomagno1, Lillian M Daughrity1, Karen Jansen-West1, Emilie A Perkerson1, Aliesha O'Raw1, Casey Cook1,2, Luc Pregent1, Veronique Belzil1, Marka van Blitterswijk1,2, Lilia J Tabassian1, Chris W Lee1,2, Mei Yue1, Jimei Tong1, Yuping Song1, Monica Castanedes-Casey1, Linda Rousseau1, Virginia Phillips1, Dennis W Dickson1,2, Rosa Rademakers1,2, John D Fryer1,2, Beth K Rush4, Otto Pedraza4, Ana M Caputo5, Pamela Desaro5, Carla Palmucci5, Amelia Robertson5, Michael G Heckman6, Nancy N Diehl6, Edythe Wiggs7, Michael Tierney7, Laura Braun7, Jennifer Farren7, David Lacomis8, Shafeeq Ladha9, Christina N Fournier10, Leo F McCluskey11, Lauren B Elman11, Jon B Toledo12,13, Jennifer D McBride13, Cinzia Tiloca14, Claudia Morelli14, Barbara Poletti14, Federica Solca14, Alessandro Prelle15, Joanne Wuu16, Jennifer Jockel-Balsarotti17, Frank Rigo18, Christine Ambrose19, Abhishek Datta20, Weixing Yang20, Denitza Raitcheva21, Giovanna Antognetti22, Alexander McCampbell23, John C Van Swieten24, Bruce L Miller25, Adam L Boxer25, Robert H Brown26, Robert Bowser9, Timothy M Miller17, John Q Trojanowski13, Murray Grossman11, James D Berry27, William T Hu10, Antonia Ratti14,28, Bryan J Traynor29, Matthew D Disney30, Michael Benatar16, Vincenzo Silani14,28, Jonathan D Glass10,31, Mary Kay Floeter7, Jeffrey D Rothstein3, Kevin B Boylan5, Leonard Petrucelli32,2.
Abstract
There is no effective treatment for amyotrophic lateral sclerosis (ALS), a devastating motor neuron disease. However, discovery of a G4C2 repeat expansion in the C9ORF72 gene as the most common genetic cause of ALS has opened up new avenues for therapeutic intervention for this form of ALS. G4C2 repeat expansion RNAs and proteins of repeating dipeptides synthesized from these transcripts are believed to play a key role in C9ORF72-associated ALS (c9ALS). Therapeutics that target G4C2 RNA, such as antisense oligonucleotides (ASOs) and small molecules, are thus being actively investigated. A limitation in moving such treatments from bench to bedside is a lack of pharmacodynamic markers for use in clinical trials. We explored whether poly(GP) proteins translated from G4C2 RNA could serve such a purpose. Poly(GP) proteins were detected in cerebrospinal fluid (CSF) and in peripheral blood mononuclear cells from c9ALS patients and, notably, from asymptomatic C9ORF72 mutation carriers. Moreover, CSF poly(GP) proteins remained relatively constant over time, boding well for their use in gauging biochemical responses to potential treatments. Treating c9ALS patient cells or a mouse model of c9ALS with ASOs that target G4C2 RNA resulted in decreased intracellular and extracellular poly(GP) proteins. This decrease paralleled reductions in G4C2 RNA and downstream G4C2 RNA-mediated events. These findings indicate that tracking poly(GP) proteins in CSF could provide a means to assess target engagement of G4C2 RNA-based therapies in symptomatic C9ORF72 repeat expansion carriers and presymptomatic individuals who are expected to benefit from early therapeutic intervention.Entities:
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Year: 2017 PMID: 28356511 PMCID: PMC5576451 DOI: 10.1126/scitranslmed.aai7866
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956