Evidence map›Paper›PMID 27164411›Full record

ArticleInternational journal of cancer2016

Deletion of macrophage migration inhibitory factor inhibits murine oral carcinogenesis: Potential role for chronic pro-inflammatory immune mediators.

Steve Oghumu, Thomas J Knobloch, Cesar Terrazas, Sanjay Varikuti, Jennifer Ahn-Jarvis, Claire E Bollinger, Hans Iwenofu, Christopher M Weghorst, Abhay R Satoskar

Open access · bronzeAbstract read
In one paragraph

Article in International journal of cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

30 citing papers in PubMed, 49 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Steve OghumuDivision of Environmental Health Sciences, College of Public Health, Ohio State University, Columbus, OH.
Thomas J KnoblochDivision of Environmental Health Sciences, College of Public Health, Ohio State University, Columbus, OH.
Cesar TerrazasDepartment of Pathology, Ohio State University Medical Center, Columbus, OH.
Sanjay VarikutiDepartment of Pathology, Ohio State University Medical Center, Columbus, OH.
Jennifer Ahn-JarvisDivision of Environmental Health Sciences, College of Public Health, Ohio State University, Columbus, OH.
Claire E BollingerDivision of Environmental Health Sciences, College of Public Health, Ohio State University, Columbus, OH.
Hans IwenofuDepartment of Pathology, Ohio State University Medical Center, Columbus, OH.
Christopher M WeghorstDivision of Environmental Health Sciences, College of Public Health, Ohio State University, Columbus, OH.
Abhay R SatoskarDepartment of Pathology, Ohio State University Medical Center, Columbus, OH.
The Ohio State University · USOhio Department of Health · USThe Ohio State University Wexner Medical Center · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Comprehensive Training in Oral &Craniofacial SciencesT32DE014320 · NIDCR · OHIO STATE UNIVERSITY · PI SHERIDAN, JOHN F · 2001 to 2022
$10.2M
Validation studies for interactive omics: Black raspberry metabolites and the oral microbiome in smokersU01CA188250 · NCI · OHIO STATE UNIVERSITY · PI CLINTON, STEVEN K, KUMAR, PURNIMA · 2014 to 2019
$3.6M
NCI NIH HHS P30 CA016058NCI NIH HHS U01 CA188250NIDCR NIH HHS T32 DE014320
6 · The paper itself

Abstract

Oral cancer kills about 1 person every hour each day in the United States and is the sixth most prevalent cancer worldwide. The pro-inflammatory cytokine 'macrophage migration inhibitory factor' (MIF) has been shown to be expressed in oral cancer patients, yet its precise role in oral carcinogenesis is not clear. In this study, we examined the impact of global Mif deletion on the cellular and molecular process occurring during oral carcinogenesis using a well-established mouse model of oral cancer with the carcinogen 4-nitroquinoline-1-oxide (4NQO). C57BL/6 Wild-type (WT) and Mif knock-out mice were administered with 4NQO in drinking water for 16 weeks, then regular drinking water for 8 weeks. Mif knock-out mice displayed fewer oral tumor incidence and multiplicity, accompanied by a significant reduction in the expression of pro-inflammatory cytokines Il-1β, Tnf-α, chemokines Cxcl1, Cxcl6 and Ccl3 and other molecular biomarkers of oral carcinogenesis Mmp1 and Ptgs2. Further, systemic accumulation of myeloid-derived tumor promoting immune cells was inhibited in Mif knock-out mice. Our results demonstrate that genetic Mif deletion reduces the incidence and severity of oral carcinogenesis, by inhibiting the expression of chronic pro-inflammatory immune mediators. Thus, targeting MIF is a promising strategy for the prevention or therapy of oral cancer.

Indexed as

AnimalsApoptosisCell Transformation, NeoplasticDisease Models, AnimalGene ExpressionGene Expression ProfilingHumansImmunologic FactorsInflammation MediatorsLymphocyte CountMacrophage Migration-Inhibitory FactorsMiceMice, KnockoutMouth NeoplasmsMyeloid CellsNeoplasm InvasivenessImmunologic FactorsInflammation MediatorsMacrophage Migration-Inhibitory FactorsTumor Suppressor Protein p53cancercytokineinflammationmyeloidoral

Identifiers

PMID27164411
PMCPMC4939094
OpenAlexW2355112289

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.