ArticleCellular & molecular biology letters2026
The role of the cGAS/STING pathway in skeletal muscle regeneration: modulation of inflammation, macrophage polarization, and oxidative stress.
Article in Cellular & molecular biology letters, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Duchenne muscular dystrophy: from gene to gene-ius therapies.Skeletal muscle · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
Abstract
backgroundSkeletal muscle regeneration is essential for restoring muscle structure and function following injury. This process is influenced by various signaling pathways. Recent studies suggest that cGAS/STING signaling, which is known for its role in innate immunity, may also play a crucial role in tissue regeneration. This study investigated the regulatory role of the cGAS/STING pathway in skeletal muscle regeneration.
methodsSkeletal muscle injury was induced via intramuscular injection of cardiotoxin (CTX) into the tibialis anterior (TA) muscle of mice. Genetic knockout models of cGAS and STING, as well as treatment with a STING agonist (DMXAA), were used to explore the role of the pathway in muscle regeneration. Histological analysis, flow cytometry, RNA extraction, and gene expression analysis were performed to evaluate muscle tissue morphology, macrophage infiltration, and the expression of inflammatory and oxidative stress markers.
resultsSTING expression was significantly increased following injury. Treatment with a STING agonist impaired muscle regeneration, characterized by reduced muscle fiber dimensions, elevated pro-inflammatory macrophage infiltration, and increased oxidative stress. In contrast, cGAS or STING knockout enhanced muscle regeneration and promoted the accumulation of anti-inflammatory macrophages.
conclusionsThe cGAS/STING pathway plays a critical role in skeletal muscle regeneration by influencing inflammation, macrophage polarization, and oxidative stress.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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 OpenQuestion graph.