ArticleCell biochemistry and biophysics2026
Immunomodulatory Activity of Sargassum thunbergii-Derived Glucuronomannan Oligomers: G6 as a Key Bioactive Component.
Article in Cell biochemistry and biophysics, 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
12 authors.
Funding
Abstract
Cyclophosphamide (CTX) is an anticancer drug known to induce immunosuppression. This study investigated the immunomodulatory effects of Sargassum thunbergii glucuronomannan and its oligomers (Gs) in CTX-induced immunosuppressive mice. Various Gs, including G2, G4, G6, G8, and Gn, were administered to the mice. Among these, G6, G8, and Gn notably improved the spleen index, cytokine levels (IL-2, IFN-γ, NO), and antioxidant activity (SOD, GSH-Px). G6 treatment increased GSH-Px by 29.3% and promoted macrophage viability. Additionally, G6 enhanced mRNA expression of iNOS, IL-2, and TNF-α. Molecular docking analysis and dynamics analysis showed strong interactions between G6 and immune cytokines IL-2 and TNF-α, enhancing receptor-binding efficiency. These results suggested that Gs, particularly G6, played a key role in immunomodulation and might serve as potential candidates.
Indexed as
Identifiers
41735756What 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.