Evidence map›Paper›PMID 32121422›Full record

ArticleInternational journal of molecular sciences2020

Butyrate Decreases ICAM-1 Expression in Human Oral Squamous Cell Carcinoma Cells.

Gabriel Leonardo Magrin, Francesca Di Summa, Franz-Josef Strauss, Layla Panahipour, Michael Mildner, Cesar Augusto Magalhães Benfatti, Reinhard Gruber

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
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  17. Molecular Mechanisms of Periodontal Disease.International journal of molecular sciences · 2021
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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

7 authors at 4 institutions in 4 countries.

Gabriel Leonardo MagrinDepartment of Oral Biology, School of Dentistry, Medical University of Vienna, Sensengasse 2a, 1090 Vienna, Austria.ORCID 0000-0003-0724-0560
Francesca Di SummaDepartment of Oral Biology, School of Dentistry, Medical University of Vienna, Sensengasse 2a, 1090 Vienna, Austria.
Franz-Josef StraussDepartment of Oral Biology, School of Dentistry, Medical University of Vienna, Sensengasse 2a, 1090 Vienna, Austria.
Layla PanahipourDepartment of Oral Biology, School of Dentistry, Medical University of Vienna, Sensengasse 2a, 1090 Vienna, Austria.ORCID 0000-0003-3557-3493
Michael MildnerDepartment of Dermatology, Medical University of Vienna, Spitalgasse 23, 1090 Vienna, Austria.ORCID 0000-0002-6892-925X
Cesar Augusto Magalhães BenfattiCenter for Education and Research on Dental Implants (CEPID), Department of Dentistry, School of Dentistry, Federal University of Santa Catarina, Campus Reitor João David Ferreira Lima s/n, Florianopolis - SC 88040-900, Brazil.ORCID 0000-0002-4209-0054
Reinhard GruberDepartment of Oral Biology, School of Dentistry, Medical University of Vienna, Sensengasse 2a, 1090 Vienna, Austria.
Medical University of Vienna · ATUniversidade Federal de Santa Catarina · BRUniversity of Bern · CHUniversity of Zurich · CH

Funding

Austrian Science Fund 4072-B28Austrian Science Fund FWF I 4072Osteology Foundation 17-125
6 · The paper itself

Abstract

Short-chain fatty acids (SCFA) are bacterial metabolites that can be found in periodontal pockets. The expression of adhesion molecules such as intercellular adhesion molecule-1 (ICAM-1) within the epithelium pocket is considered to be a key event for the selective transmigration of leucocytes towards the gingival sulcus. However, the impact of SCFA on ICAM-1 expression by oral epithelial cells remains unclear. We therefore exposed the oral squamous carcinoma cell line HSC-2, primary oral epithelial cells and human gingival fibroblasts to SCFA, namely acetate, propionate and butyrate, and stimulated with known inducers of ICAM-1 such as interleukin-1-beta (IL1β) and tumor necrosis factor-alfa (TNFα). We report here that butyrate but not acetate or propionate significantly suppressed the cytokine-induced ICAM-1 expression in HSC-2 epithelial cells and primary epithelial cells. The G-protein coupled receptor-43 (GPR43/ FFAR2) agonist but not the histone deacetylase inhibitor, trichostatin A, mimicked the butyrate effects. Butyrate also attenuated the nuclear translocation of p65 into the nucleus on HSC-2 cells. The decrease of ICAM-1 was independent of Nrf2/HO-1 signaling and phosphorylation of JNK and p38. Nevertheless, butyrate could not reverse an ongoing cytokine-induced ICAM-1 expression in HSC-2 cells. Overall, these observations suggest that butyrate can attenuate cytokine-induced ICAM-1 expression in cells with epithelial origin.

Indexed as

AcetatesButyratesCarcinoma, Squamous CellCell Line, TumorEpithelial CellsFatty Acids, VolatileFibroblastsGene Expression Regulation, NeoplasticHumansIntercellular Adhesion Molecule-1Interleukin-1betaMouth NeoplasmsNF-E2-Related Factor 2PropionatesReceptors, Cell SurfaceReceptors, G-Protein-CoupledAcetatesButyratesFatty Acids, VolatileFFAR2 protein, humanICAM1 protein, humanIL1B protein, humanIntercellular Adhesion Molecule-1Interleukin-1betaNFE2L2 protein, humanNF-E2-Related Factor 2PropionatesReceptors, Cell SurfaceReceptors, G-Protein-Coupledbutyric acidepithelial cellsintercellular adhesion molecule-1in vitrooral biologyperiodontium

Identifiers

PMID32121422
PMCPMC7084181
OpenAlexW3009533466

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.