Evidence map›Paper›PMID 27371534›Full record

ArticleGut2017

Hemidesmosome integrity protects the colon against colitis and colorectal cancer.

Adèle De Arcangelis, Hussein Hamade, Fabien Alpy, Sylvain Normand, Emilie Bruyère, Olivier Lefebvre, Agnès Méchine-Neuville, Stéphanie Siebert, Véronique Pfister, Patricia Lepage and 11 more

Open access · hybridAbstract read
In one paragraph

Article in Gut, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
8.1field-weighted citation impact, top 3% of its field
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

55 citing papers in PubMed, 98 citations in OpenAlex.

  1. Trial
  2. Observational
  3. Integrin α6 Targeted Tumor Theranostics.Phenomics (Cham, Switzerland) · 2025
    Review
  4. Review
  5. Threonine phosphorylation of STAT1 safeguards gut epithelial integrity and restricts interferon-mediated cytotoxicity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Noncanonical functions of adhesion proteins in inflammation.American journal of physiology. Cell physiology · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Loss of ERβ in Aging LXRαβ Knockout Mice Leads to Colitis.International journal of molecular sciences · 2023
    Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 4 institutions in 3 countries.

Adèle De ArcangelisDepartment of Development and Stem Cells, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Université de Strasbourg, Illkirch, France.
Hussein HamadeDepartment of Development and Stem Cells, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Université de Strasbourg, Illkirch, France.
Fabien AlpyInserm, U964, Illkirch, France.
Sylvain NormandCNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR 8204-CIIL-Centre d'Infection et d'Immunité de Lille, Université de Lille, Lille, France.
Emilie BruyèreInserm, Université de Lille, CHRU Lille, UMR-S 1172-Jean-Pierre Aubert Research Center, Lille, France.
Olivier LefebvreUniversité de Strasbourg, Strasbourg, France.
Agnès Méchine-NeuvilleInserm, U1109, MNT3 Team, Strasbourg, France.
Stéphanie SiebertDepartment of Development and Stem Cells, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Université de Strasbourg, Illkirch, France.
Véronique PfisterDepartment of Development and Stem Cells, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Université de Strasbourg, Illkirch, France.
Patricia LepageUMR1319-MICALIS Institute, INRA, AgroParisTech,Université Paris-Saclay, Jouy-en-Josas, France.
Patrice LaquerriereUniversité de Strasbourg, Strasbourg, France.
Doulaye DembeleDepartment of Development and Stem Cells, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Université de Strasbourg, Illkirch, France.
Anne Delanoye-CrespinCNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR 8204-CIIL-Centre d'Infection et d'Immunité de Lille, Université de Lille, Lille, France.
Sophie RodiusDepartment of Development and Stem Cells, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Université de Strasbourg, Illkirch, France.
Sylvie RobineInstitut Curie, Paris, France.
Michèle KedingerUniversité de Strasbourg, Strasbourg, France.
Isabelle Van SeuningenInserm, Université de Lille, CHRU Lille, UMR-S 1172-Jean-Pierre Aubert Research Center, Lille, France.
Patricia Simon-AssmannUniversité de Strasbourg, Strasbourg, France.
Mathias ChamaillardCNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR 8204-CIIL-Centre d'Infection et d'Immunité de Lille, Université de Lille, Lille, France.
Michel LabouesseDepartment of Development and Stem Cells, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Université de Strasbourg, Illkirch, France.
Elisabeth Georges-LabouesseDepartment of Development and Stem Cells, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Université de Strasbourg, Illkirch, France.
Centre National de la Recherche Scientifique · FRInserm · FRAgroParisTech · FRCedars-Sinai Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveEpidemiological and clinical data indicate that patients suffering from IBD with long-standing colitis display a higher risk to develop colorectal high-grade dysplasia. Whereas carcinoma invasion and metastasis rely on basement membrane (BM) disruption, experimental evidence is lacking regarding the potential contribution of epithelial cell/BM anchorage on inflammation onset and subsequent neoplastic transformation of inflammatory lesions. Herein, we analyse the role of the α6β4 integrin receptor found in hemidesmosomes that attach intestinal epithelial cells (IECs) to the laminin-containing BM.

designWe developed new mouse models inducing IEC-specific ablation of α6 integrin either during development (α6

resultsStrikingly, all α6

conclusionsWe provide for the first time evidence that loss of IECs/BM interactions triggered by hemidesmosome disruption initiates the development of inflammatory lesions that progress into high-grade dysplasia and carcinoma. Colorectal neoplasia in our mouse models resemble that seen in patients with IBD, making them highly attractive for discovering more efficient therapies.

Indexed as

Adaptive ImmunityAdenocarcinomaAnimalsBasement MembraneB-LymphocytesCaspase 1ColitisColorectal NeoplasmsCytokinesEpithelial CellsHemidesmosomesHomeostasisIntegrin alpha6Integrin alpha6beta4Intestinal MucosaKeratin-18Caspase 1CytokinesIntegrin alpha6Integrin alpha6beta4Keratin-18Keratin-8Myd88 protein, mouseMyeloid Differentiation Factor 88CELL MATRIX INTERACTIONCOLORECTAL CANCERIBDINTEGRINSINTESTINAL BARRIER FUNCTION

Identifiers

PMID27371534
PMCPMC5595104
OpenAlexW2470083245

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.