ArticleJournal of cellular and molecular medicine2026
Systematic Identification and Functional Validation of CASP10 as a DNA-Damage-Responsive Driver of Endothelial Pyroptosis in Atherosclerosis.
Article in Journal of cellular and molecular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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Who cites it
2 citing papers in PubMed.
- Systematic Identification and Functional Validation of CASP10 as a DNA-Damage-Responsive Driver of Endothelial Pyroptosis in Atherosclerosis.Journal of cellular and molecular medicine · 2026Article
- Article
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Authors and funding
6 authors.
Funding
Abstract
Atherosclerosis (AS) is a chronic inflammatory disease driven by endothelial dysfunction and plaque instability. The DNA damage response (DDR) has been implicated in endothelial cell fate; its precise role in AS remains unclear. This study aims to identify DDR-related biomarkers associated with AS and elucidate their mechanisms in endothelial pyroptosis. Our analysis identified 66 DDR-related genes, which achieved over 80% accuracy in discriminating early from advanced lesions and hemorrhagic from non-hemorrhagic plaques in external datasets, and reached 100% accuracy in differentiating plaque stability. CASP10 emerged as a top diagnostic biomarker (AUC = 0.991) compared to other DDR genes. Single-cell analysis confirmed elevated CASP10 expression in endothelial cells of AS plaques. Functional experiments revealed that CASP10 is both necessary and sufficient for ox-LDL-induced DNA damage and pyroptosis in HUVECs. CASP10 overexpression exacerbated γH
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