ReviewRSC chemical biology2026
Facilitated DNA damage repair as an emerging therapeutic strategy for inflammatory and fibrotic diseases.
Review in RSC chemical biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
DNA damage arising from metabolic stress, oxidative injury, and impaired genome maintenance emerges as a common driver for chronic inflammatory and fibrotic diseases across multiple organs. While rapid and effective DNA damage repair is essential for the response to acute injury, sustained activation of these pathways promotes cellular senescence, sterile inflammation and fibroblast activation, ultimately driving fibrogenesis and pathological tissue remodelling. In recent years, DNA repair processes, particularly base excision repair in both the nucleus and mitochondria, receive increasing attention as modulators of inflammatory and fibrotic outcomes. Here, we review the molecular mechanisms by which unresolved nuclear and mitochondrial DNA lesions translate into chronic inflammation and fibrosis across skin, liver, lung and cardiovascular tissues. We discuss the roles of chromatin context, NAD
Identifiers
What Socratic 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 Socratic graph.