Evidence map›Paper›PMID 39723693›Full record

ReviewBioEssays : news and reviews in molecular, cellular and developmental biology2025

New Horizons in Myotonic Dystrophy Type 1: Cellular Senescence as a Therapeutic Target.

Cécilia Légaré, J Andrew Berglund, Elise Duchesne, Nicolas A Dumont

Abstract readReview
In one paragraph

Review in BioEssays : news and reviews in molecular, cellular and developmental biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

4 authors.

Cécilia LégaréRNA Institute, College of Arts and Sciences, University at Albany-SUNY, Albany, New York, USA.
J Andrew BerglundRNA Institute, College of Arts and Sciences, University at Albany-SUNY, Albany, New York, USA.
Elise DuchesneSchool of Rehabilitation Sciences, Faculty of Medicine, Université Laval, Quebec, Quebec, Canada.
Nicolas A DumontCHU Sainte-Justine Research Center, Montreal, Quebec, Canada.ORCID https://orcid.org/0000-0002-7536-1666

Funding

Design, Synthesis and Efficacy of New Small Molecule Therapeutics to Impede Myotonic DystrophyR01NS120485 · NINDS · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI Andrew Berglund, Masayuki Nakamori · 2022 to 2026
$2.7M
Alternative Splicing and Development of Small Molecule Therapeutics in CAG Expansion Spinocerebellar AtaxiasR01NS135254 · NINDS · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI Andrew Berglund, Damian Seung-Ho Shin · 2024 to 2026
$2.0M
Institute of Musculoskeletal Health and Arthritis PJT-186092Muscular Dystrophy Association 1192211Muscular Dystrophy Canada 855145NIH HHS R01NS12048501NINDS NIH HHS R01 NS120485NINDS NIH HHS R01 NS135254U.S. Army Medical Research Acquisition Activity PR231850
6 · The paper itself

Abstract

Myotonic dystrophy type 1 (DM1) is considered a progeroid disease (i.e., causing premature aging). This hypervariable disease affects multiple systems, such as the musculoskeletal, central nervous, gastrointestinal, and others. Despite advances in understanding the underlying pathogenic mechanism of DM1, numerous gaps persist in our understanding, hindering elucidation of the heterogeneity and severity of its symptoms. Accumulating evidence indicates that the toxic intracellular RNA accumulation associated with DM1 triggers cellular senescence. These cells are in a state of irreversible cell cycle arrest and secrete a cocktail of cytokines, referred to as a senescence-associated secretory phenotype (SASP), that can have harmful effects on neighboring cells and more broadly. We hypothesize that cellular senescence contributes to the pathophysiology of DM1, and clearance of senescent cells is a promising therapeutic approach for DM1. We will discuss the therapeutic potential of different senotherapeutic drugs, especially senolytics that eliminate senescent cells, and senomorphics that reduce SASP expression.

Indexed as

Cellular SenescenceMyotonic DystrophySenotherapeuticsAnimalsHumansSenescence-Associated Secretory PhenotypeSenotherapeuticsmyotonic dystrophy Type 1senescencesenolyticssenomorphics

Identifiers

PMID39723693
PMCPMC11848125

What Socratic holds

Textmetadata
LicenceTDM
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.