Evidence map›Paper›PMID 23125418›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2012

Macrophage migration inhibitory factor promotes tumor growth and metastasis by inducing myeloid-derived suppressor cells in the tumor microenvironment.

Kendra D Simpson, Dennis J Templeton, Janet V Cross

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 141 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
141citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 5% 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

141 citing papers in PubMed, 1 synthesis or guideline pooled it, 213 citations in OpenAlex.

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  20. Multifactoral immune modulation potentiates durable remission in multiple models of aggressive malignancy.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article

81 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Kendra D SimpsonDepartment of Pathology, University of Virginia, Charlottesville, VA 22908, USA.
Dennis J Templeton
Janet V Cross
University of Virginia · US

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Thomas P. Loughran · 1987 to 2026
$72.1M
TRAINING IN THE PHARMACOLOGICAL SCIENCEST32GM007055 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LYNCH, KEVIN R. · 1985 to 2022
$7.2M
Function of a molecular target of cancer chemopreventionR01CA113899 · NCI · UNIVERSITY OF VIRGINIA · PI TEMPLETON, DENNIS J · 2006 to 2010
$1.7M
An anti-inflammatory role for bioactive nutrient isothiocyanatesR01AT004323 · NCCIH · UNIVERSITY OF VIRGINIA · PI CROSS, JANET V · 2007 to 2010
$1.3M
NCCIH NIH HHS R01 AT004323NCCIH NIH HHS R01AT004323NCI NIH HHS P30 CA044579NCI NIH HHS P30 CA44579NCI NIH HHS R01 CA113899NCI NIH HHS R01CA113899NIGMS NIH HHS T32 GM007055
6 · The paper itself

Abstract

The macrophage migration inhibitory factor (MIF), an inflammatory cytokine, is overexpressed in many solid tumors and is associated with poor prognosis. We previously identified inhibitors of MIF within a class of natural products with demonstrated anti-cancer activities. We therefore sought to determine how MIF contributes to tumor growth and progression. We show in this study that in murine tumors including the 4T1 model of aggressive, spontaneously metastatic breast cancer in immunologically intact mice, tumor-derived MIF promotes tumor growth and pulmonary metastasis through control of inflammatory cells within the tumor. Specifically, MIF increases the prevalence of a highly immune suppressive subpopulation of myeloid-derived suppressor cells (MDSCs) within the tumor. In vitro, MIF promotes differentiation of myeloid cells into the same population of MDSCs. Pharmacologic inhibition of MIF reduces MDSC accumulation in the tumor similar to MIF depletion and blocks the MIF-dependent in vitro differentiation of MDSCs. Our results demonstrate that MIF is a therapeutically targetable mechanism for control of tumor growth and metastasis through regulation of the host immune response and support the potential utility of MIF inhibitors, either alone or in combination with standard tumor-targeting therapeutic or immunotherapy approaches.

Indexed as

AnimalsCell DifferentiationCell Line, TumorFemaleInflammationIntramolecular OxidoreductasesLung NeoplasmsMacrophage Migration-Inhibitory FactorsMammary Neoplasms, ExperimentalMiceMice, Inbred BALB CMice, SCIDMyeloid Progenitor CellsSkin NeoplasmsTumor MicroenvironmentIntramolecular OxidoreductasesMacrophage Migration-Inhibitory FactorsMif protein, mouse

Identifiers

PMID23125418
PMCPMC3518629
OpenAlexW1893818399

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.