ArticleCell death & disease2026
Restoring O-glycosylation and expression of MUC2 limits progression of colorectal cancer.
Article in Cell death & disease, 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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Intestinal Mucin Glycosylation: Structural Regulation, Homeostasis Maintenance and Disease Association.Biomolecules · 2025Review
- UnravelingAnalytical chemistry · 2024Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
Abstract
Colorectal cancer (CRC) progression is associated with intestinal barrier dysfunction, yet the molecular mechanisms governing mucin glycosylation remain unclear. This study aims to investigate the regulatory pathway controlling MUC2 expression and O-glycosylation in CRC and assess the therapeutic potential of rosiglitazone in restoring mucosal integrity. In this study, B3GNT6 was identified as a key glycosyltransferase that promotes MUC2 O-glycosylation and protein stability. KLF4 was shown to transcriptionally regulate both B3GNT6 and MUC2, with its activity modulated by PPARg. Treatment with the PPARg agonist rosiglitazone activated the PPARg-KLF4-B3GNT6 axis, restoring MUC2 function and enhancing the mucus barrier integrity. These findings highlight a novel therapeutic avenue for CRC by targeting mucin glycosylation.
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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.