ArticleRenal failure2025
Mechanism of
Article in Renal failure, 2025. 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.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundAlthough
methodsActive compounds of
resultsThe top 10 core targets were identified, namely PPARG, AKT1, EGFR, STAT3, CASP3, PPARA, ICAM1, PTGS2, SRC, and MMP9. Enrichment analysis revealed that the primary pathways involving these targets including prolactin signaling pathway, AGE-RAGE signaling pathway in diabetic complications, TNF signaling pathway, relaxin signaling pathway, VEGF signaling pathway, and FoxO signaling pathway. Molecular docking demonstrated that mandenol exhibited a strong binding affinity toward EGFR domain, and wallichilide displayed pronounced binding affinity toward AKT1, EGFR, STAT3, and PTGS2 domains. Additionally, myricanone and senkyunone also showed strong binding affinity for AKT1, EGFR, CASP3, STAT3, and PTGS2 domains.
conclusionsThis study revealed the potential multi-component and multi-target mechanisms of
Indexed as
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.