Evidence map›Paper›PMID 26763429›Full record

ArticleThe Journal of investigative dermatology2016

Increased Bacterial Load and Expression of Antimicrobial Peptides in Skin of Barrier-Deficient Mice with Reduced Cancer Susceptibility.

Ken Natsuga, Sara Cipolat, Fiona M Watt

Erratum issuedOpen access · hybridAbstract readComparative Study
In one paragraph

Article in The Journal of investigative dermatology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Adding Fuel to the Fire? The Skin Microbiome in Atopic Dermatitis.The Journal of investigative dermatology · 2024
    Review
  3. Article
  4. The Human Microbiota and Skin Cancer.International journal of molecular sciences · 2022
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Loricrin: Past, Present, and Future.International journal of molecular sciences · 2020
    Review
  10. Review
  11. The role of the skin microbiome in atopic dermatitis.Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2019
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

Ken NatsugaCancer Research UK Cambridge Research Institute, Li Ka Shing Centre, Cambridge, United Kingdom; Department of Dermatology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Sara CipolatCancer Research UK Cambridge Research Institute, Li Ka Shing Centre, Cambridge, United Kingdom; Centre for Stem Cells and Regenerative Medicine, King's College London, London, United Kingdom.
Fiona M WattCentre for Stem Cells and Regenerative Medicine, King's College London, London, United Kingdom. Electronic address: Fiona.watt@kcl.ac.uk.
Cancer Research UK Cambridge Center · GBKing's College London · GB

Funding

Medical Research Council G1100073Medical Research Council MR/L022699/1Wellcome Trust 096540
6 · The paper itself

Abstract

Mice lacking three epidermal barrier proteins-envoplakin, periplakin, and involucrin (EPI-/- mice)-have a defective cornified layer, reduced epidermal γδ T cells, and increased dermal CD4(+) T cells. They are also resistant to developing skin tumors. The tumor-protective mechanism involves signaling between Rae-1 expressing keratinocytes and the natural killer group 2D receptor on immune cells, which also plays a role in host defenses against infection. Given the emerging link between bacteria and cancer, we investigated whether EPI-/- mice have an altered skin microbiota. The bacterial phyla were similar in wild-type and EPI-/- skin. However, bacteria were threefold more abundant in EPI-/- skin and penetrated deeper into the epidermis. The major epithelial defense mechanism against bacteria is production of antimicrobial proteins (AMPs). EPI-/- skin exhibited enhanced expression of antimicrobial peptides. However, reducing the bacterial load by antibiotic treatment or breeding mice under specific pathogen-free conditions did not reduce AMP expression or alleviate the abnormalities in T-cell populations. We conclude that the atopic characteristics of EPI-/- skin are a consequence of the defective barrier rather than a response to the increased bacterial load. It is therefore unlikely that the increase in skin microbiota contributes directly to the observed cancer resistance.

Indexed as

Analysis of VarianceAnimalsAnti-Bacterial AgentsAntimicrobial Cationic PeptidesBacterial LoadDisease Models, AnimalDisease SusceptibilityEnzyme-Linked Immunosorbent AssayFemaleIn Situ Hybridization, FluorescenceMembrane ProteinsMiceMice, Inbred C57BLMicrobiotaPeroxidaseProtein PrecursorsAnti-Bacterial AgentsAntimicrobial Cationic PeptidesenvoplakininvolucrinMembrane ProteinsPeroxidaseProtein Precursors

Identifiers

PMID26763429
PMCPMC4759621
OpenAlexW2175948593

What OpenQuestion holds

Textmetadata
LicenceTDM
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.