Evidence map›Paper›PMID 23390297›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Control of tumor-associated macrophage alternative activation by macrophage migration inhibitory factor.

Kavitha Yaddanapudi, Kalyani Putty, Beatriz E Rendon, Gwyneth J Lamont, Jonathan D Faughn, Abhay Satoskar, Amanda Lasnik, John W Eaton, Robert A Mitchell

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

111 citing papers in PubMed, 191 citations in OpenAlex.

  1. Trial
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  5. CDK4/6 Inhibition Induces CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Spatial Profiling Identifies Tumor-Associated Stroma Enrichment and MIF as Potential Immunotherapy Targets in Primary Ewing Sarcomas.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review

51 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

9 authors at 3 institutions in 1 country.

Kavitha YaddanapudiMolecular Targets Group, J.G. Brown Cancer Center, University of Louisville, Louisville, KY 40202, USA.
Kalyani Putty
Beatriz E Rendon
Gwyneth J Lamont
Jonathan D Faughn
Abhay Satoskar
Amanda Lasnik
John W Eaton
Robert A Mitchell
University of Louisville · USTarget (United States) · USThe Ohio State University · US

Funding

PROJ 12: STEM CELL-BASED VACCINE FOR CANCER PROPHYLAXISP20RR018733 · NCRR · UNIVERSITY OF LOUISVILLE · PI TRENT, JOHN O · 2003 to 2011
$18.9M
Amplification of tumor hypoxic responses by MIF-dependent HIF stabilizationR01CA129967 · NCI · UNIVERSITY OF LOUISVILLE · PI MITCHELL, ROBERT A · 2009 to 2013
$1.5M
NCI NIH HHS CA129967NCI NIH HHS R01 CA129967NCRR NIH HHS P20 RR018733NCRR NIH HHS P20RR018733
6 · The paper itself

Abstract

Tumor stromal alternatively activated macrophages are important determinants of antitumor T lymphocyte responses, intratumoral neovascularization, and metastatic dissemination. Our recent efforts to investigate the mechanism of macrophage migration inhibitory factor (MIF) in antagonizing antimelanoma immune responses reveal that macrophage-derived MIF participates in macrophage alternative activation in melanoma-bearing mice. Both peripheral and tumor-associated macrophages (TAMs) isolated from melanoma bearing MIF-deficient mice display elevated proinflammatory cytokine expression and reduced anti-inflammatory, immunosuppressive, and proangiogenic gene products compared with macrophages from tumor-bearing MIF wild-type mice. Moreover, TAMs and myeloid-derived suppressor cells from MIF-deficient mice exhibit reduced T lymphocyte immunosuppressive activities compared with those from their wild-type littermates. Corresponding with reduced tumor immunosuppression and neo-angiogenic potential by TAMs, MIF deficiency confers protection against transplantable s.c. melanoma outgrowth and melanoma lung metastatic colonization. Finally, we report for the first time, to our knowledge, that our previously discovered MIF small molecule antagonist, 4-iodo-6-phenylpyrimidine, recapitulates MIF deficiency in vitro and in vivo, and attenuates tumor-polarized macrophage alternative activation, immunosuppression, neoangiogenesis, and melanoma tumor outgrowth. These studies describe an important functional contribution by MIF to TAM alternative activation and provide justification for immunotherapeutic targeting of MIF in melanoma patients.

Indexed as

AnimalsCarcinoma, Lewis LungCell Line, TumorCells, CulturedLung NeoplasmsMacrophage ActivationMacrophage Migration-Inhibitory FactorsMacrophages, PeritonealMaleMelanoma, ExperimentalMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicMacrophage Migration-Inhibitory Factors

Identifiers

PMID23390297
PMCPMC3593945
OpenAlexW2142394051

What OpenQuestion holds

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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.