ArticleFrontiers in immunology2026
Danthron as a novel IL-6R agonist promotes thrombopoiesis via the SRC/RAS/MAPK pathway.
Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
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Who cites it
1 citing paper in PubMed.
- GLSP ameliorates monocrotaline-induced pulmonary arterial hypertension through inhibition of the PI3K/AKT and MAPK signaling pathways.Journal of molecular histology · 2026Article
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13 authors.
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Abstract
Background: This study aimed to investigate the effects of danthron on promoting megakaryocyte (MK) differentiation and alleviating thrombocytopenia, as well as to elucidate its underlying mechanisms. Methods: Cell proliferation and apoptosis of Meg-01 and K562 cells were evaluated by CCK-8, LDH release, and apoptosis assays. MK differentiation was assessed by Giemsa staining, phalloidin staining, and flow cytometry. A thrombocytopenia mouse model was induced by 4 Gy irradiation and treated intraperitoneally with danthron for 12 days, followed by hematological, histopathological, MK differentiation, and tail bleeding analyses. Potential targets and pathways were explored using network pharmacology, molecular docking, GO/KEGG enrichment, Western blotting, and inhibitor validation. Results: Danthron effectively promoted MK differentiation Conclusion: This study uncovered danthron as a novel natural small-molecule agonist of IL-6R and demonstrated its therapeutic potential in thrombocytopenia. The effect of danthron is mediated by its capacity to promote MK differentiation and induce platelet production through targeting of IL-6R and activation of the downstream SRC/RAS/MAPK signaling pathway. These results highlight danthron as a promising candidate for thrombocytopenia therapy and underscore the therapeutic potential of targeting IL-6R signaling for hematopoietic regulation.
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