Evidence map›Paper›PMID 42033225›Full record

ArticleNucleic acids research2026

Direct targeting of C9ORF72 repeat RNA with fluorinated antisense oligonucleotides.

Halle M Barber, Mansi A Parasrampuria, Jerónimo Jurado-Arjona, Andrea Gamir-Morralla, Benedikt Berninger, Carlos González, Keith T Gagnon, Masad J Damha, Miguel Garavís

Abstract read
In one paragraph

Article in Nucleic acids research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Halle M BarberDepartment of Chemistry, McGill University, Montreal, QC H3A 0B8, Canada.ORCID 0000-0003-3514-7240
Mansi A ParasrampuriaBiochemistry and Molecular Biology, Wake Forest University School of Medicine, Winston-Salem, NC 27101, United States.
Jerónimo Jurado-ArjonaCentre for Developmental Neurobiology, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London SE1 1UL, United Kingdom.
Andrea Gamir-MorrallaCentre for Developmental Neurobiology, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London SE1 1UL, United Kingdom.
Benedikt BerningerCentre for Developmental Neurobiology, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London SE1 1UL, United Kingdom.
Carlos GonzálezInstituto de Química Física 'Blas Cabrera', IQF-CSIC, Madrid 28006, Spain.
Keith T GagnonBiochemistry and Molecular Biology, Wake Forest University School of Medicine, Winston-Salem, NC 27101, United States.ORCID 0000-0002-5868-675X
Masad J DamhaDepartment of Chemistry, McGill University, Montreal, QC H3A 0B8, Canada.ORCID 0000-0002-4458-1623
Miguel GaravísInstituto de Química Física 'Blas Cabrera', IQF-CSIC, Madrid 28006, Spain.ORCID 0000-0003-1889-1713

Funding

CSIC RYC2023-043599-IERA-NET Neuron P2024-02-015European Union Marie Skłodowska-Curie Actions MSCA-IF-750624European Union Marie Skłodowska-Curie Actions MSCA-IF-799693European Union Marie Skłodowska-Curie Actions MSCA-IF-841260Fonds de Recherche du QuébecMinisterio de Ciencia e Innovación PID2023-146366NB-I00Natural Sciences and Engineering Research Council of Canada #2022-03372NIH HHS 1R01GM135646-01
6 · The paper itself

Abstract

Hexanucleotide repeat expansions in the C9ORF72 gene are the most common genetic cause of amyotrophic lateral sclerosis and frontotemporal dementia. These expansions give rise to pathogenic sense and antisense repeat RNAs that form nuclear foci and undergo repeat-associated non-AUG translation, producing dipeptide repeat proteins with cellular toxicity. Directly targeting the causative repeat RNAs with antisense oligonucleotides represents a promising therapeutic strategy. One barrier to further development is the propensity of this G-rich repeat-containing RNA target to form stable secondary structures, which may hinder efficient hybridization. In this study, we designed a panel of fluorine-modified ASOs that target the sense repeat expansions. We identified C-rich F-ASO gapmers that reduced translation from sense repeat RNAs in a cell-based reporter assay and lowered the RNA foci burden in patient-derived cells. Structural analyses in vitro revealed that the 2'F-RNA gapmer formed a stable hairpin structure. Our results demonstrate that structural properties of fluorine modifications can be leveraged for effective binding of repeat RNA and highlight the potential for F-ASOs to serve as therapeutic tools when targeting toxic repeat RNAs in C9ORF72-mediated FTD/ALS and other repeat expansion diseases.

Indexed as

C9orf72 ProteinDNA Repeat ExpansionFluorineOligonucleotides, AntisenseRNAAmyotrophic Lateral SclerosisHumansNucleic Acid ConformationC9orf72 ProteinC9orf72 protein, humanFluorineOligonucleotides, AntisenseRNA

Identifiers

PMID42033225
PMCPMC13109722

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.