Evidence map›Paper›PMID 39926604›Full record

ArticleFrontiers in immunology2024

MUC2 expression modulates immune infiltration in colorectal cancer.

Christophe M Raynaud, Ayesha Jabeen, Eiman I Ahmed, Satanay Hubrack, Apryl Sanchez, Shimaa Sherif, Ahmad A Al-Shaibi, Bernice Lo, Jessica Roelands, Davide Bedognetti and 1 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. The Power of MUC2 in Mucinous Adenocarcinomas.Pathobiology : journal of immunopathology, molecular and cellular biology · 2026
    Review
  7. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Christophe M RaynaudTumor Biology and Immunology Laboratory, Research Branch, Sidra Medicine, Doha, Qatar.
Ayesha JabeenTumor Biology and Immunology Laboratory, Research Branch, Sidra Medicine, Doha, Qatar.
Eiman I AhmedTumor Biology and Immunology Laboratory, Research Branch, Sidra Medicine, Doha, Qatar.
Satanay HubrackLaboratory of immunoregulation, Research Branch, Sidra Medicine, Doha, Qatar.
Apryl SanchezTumor Biology and Immunology Laboratory, Research Branch, Sidra Medicine, Doha, Qatar.
Shimaa SherifTumor Biology and Immunology Laboratory, Research Branch, Sidra Medicine, Doha, Qatar.
Ahmad A Al-ShaibiLaboratory of immunoregulation, Research Branch, Sidra Medicine, Doha, Qatar.
Bernice LoLaboratory of immunoregulation, Research Branch, Sidra Medicine, Doha, Qatar.
Jessica RoelandsDepartment of Pathology, Leiden University Medical Center, Leiden, Netherlands.
Davide BedognettiTumor Biology and Immunology Laboratory, Research Branch, Sidra Medicine, Doha, Qatar.
Wouter HendrickxTumor Biology and Immunology Laboratory, Research Branch, Sidra Medicine, Doha, Qatar.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Colorectal cancer (CRC) is a prevalent malignancy with significant morbidity and mortality worldwide. A deeper understanding of the interaction of cancer cells with other cells in the tumor microenvironment is crucial to devise effective therapeutic strategies. MUC2, a major component of the protective mucus layer in the gastrointestinal tract, has been implicated in CRC progression and immune response regulation. Method: In this study, we sought to elucidate the relationship between MUC2 expression and immune infiltration within CRC using Results: While MUC2 was more abundant in LS-174T cell line compared to HT-29, its knockout resulted in increased immune infiltration solely in the HT-29 cell line, but not in the LS-174T cell line. We revealed that the removal of MUC2 protein was compensated in LS-174T by the expression of other gel-forming mucin proteins (MUC6, MUC5B) commonly expressed in the gastrointestinal epithelium, while this was not observed in HT-29 cell line. Conclusion: Our study is the first to demonstrate that MUC2 functions as a physical barrier to immune infiltration in colorectal cancer (CRC)

Indexed as

Colorectal NeoplasmsLymphocytes, Tumor-InfiltratingMucin-2Cell Line, TumorGene Expression Regulation, NeoplasticHT29 CellsHumansKiller Cells, NaturalMucin-5BTumor MicroenvironmentMUC2 protein, humanMucin-2Mucin-5Bcolon cancerimmune infiltrationMUC2mucinsspheroids

Identifiers

PMID39926604
PMCPMC11802499

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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 OpenQuestion graph.