ArticleCell biochemistry and biophysics2025
Lysine Demethylase 5B Alleviates Neuroinflammation in Ischemic Stroke by Repressing Steap4.
Article in Cell biochemistry and biophysics, 2025. 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
5 authors.
Funding
Abstract
Six-transmembrane epithelial antigen of prostate 4 (Steap4) has been suggested as a potential marker for reactive astrocytes. This investigation focuses on the role of Steap4 in ischemic stroke (IS) and its regulator in this context. A mouse model of IS was generated using middle cerebral artery occlusion (MCAO). Additionally, mouse astrocytes that underwent oxygen-glucose deprivation (OGD) were utilized for in vitro investigations. Steap4 was found to be upregulated in the brain of MCAO-challenged mice and OGD-challenged astrocytes. Steap4 silencing reduced infarct size and alleviated IS-associated pathological exacerbations in mice, as well as ameliorated A1 skewing of astrocytes and inflammatory cytokine secretion both in vivo and in vitro. Lysine demethylase 5B (Kdm5b), identified as an upstream regulator of Steap4, was poorly expressed in IS/OGD models. Kdm5b overexpression repressed Steap4 transcription by removing H3K4me3 modification, thus alleviating pro-inflammatory activation of astrocytes and neuroinflammation. However, Kdm5b's protective effects were diminished upon Steap4 restoration in mice or astrocytes. In conclusion, this study suggests that the loss of Kdm5b leads to aberrant upregulation of Steap4, contributing to pro-inflammatory activation of astrocytes and brain damage in IS.
Indexed as
Identifiers
40448887What 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.