Evidence map›Paper›PMID 20581170›Full record

ArticleAmerican journal of respiratory and critical care medicine2010

Macrophage migration inhibitory factor promotes tumor growth in the context of lung injury and repair.

Douglas Arenberg, Tracy R Luckhardt, Shannon Carskadon, Liujian Zhao, Mohammad A Amin, Alisa E Koch

Abstract readEvaluation Study
In one paragraph

Article in American journal of respiratory and critical care medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Role of macrophage migration inhibitory factor in age-related lung disease.American journal of physiology. Lung cellular and molecular physiology · 2015
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Update in lung cancer and oncological disorders 2010.American journal of respiratory and critical care medicine · 2011
    Article
  14. Update in acute lung injury and critical care 2010.American journal of respiratory and critical care medicine · 2011
    Review
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

6 authors at 1 institution in 1 country.

Douglas ArenbergDivision of Pulmonary and Critical Care Medicine, University of Michigan Medical Center, Ann Arbor, Michigan 48109-0642, USA. darenber@umich.edu
Tracy R Luckhardt
Shannon Carskadon
Liujian Zhao
Mohammad A Amin
Alisa E Koch
University of Michigan · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
Promotion of Angiogenesis in Lung Cancer by MIFR01CA094121 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ARENBERG, DOUGLAS · 2002 to 2010
$1.9M
IL-18 in rheumatoid inflammation and angiogenesisR01AR048267 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KOCH, ALISA E · 2003 to 2007
$1.4M
Role of the 4A11 antigen in rheumatoid arthritisR03AR052482 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI AMIN, MOHAMMAD A · 2006 to 2008
$221k
NCI NIH HHS CA46592NCI NIH HHS P30 CA046592NCI NIH HHS R01-CA94121NIAMS NIH HHS R01-AR48267NIAMS NIH HHS R03 AR052482
6 · The paper itself

Abstract

rationaleTissue injury and repair involve highly conserved processes governed by mechanisms that can be co-opted in tumors. We hypothesized that soluble factors released during the repair response to lung injury would promote orthotopic tumor growth.

objectivesTo determine whether lung injury promoted growth of orthotopic lung tumors and to study the molecular mechanisms.

methodsWe initiated lung injury in C57Bl6 mice using different stimuli, then injected Lewis lung carcinoma cells during the repair phase. We assessed tumor growth 14 days later. We measured tumor angiogenesis, cytokine expression, proliferation, and apoptosis. MEASUREMENTS AND MAIN

resultsRegardless of the mechanism, injured lungs contained more numerous and larger tumors than sham-injured lungs. Tumors from injured lungs were no more vascular, but had higher levels of proliferation and reduced rates of apoptosis. The cytokine macrophage migration inhibitory factor (MIF) was highly expressed in both models of tissue injury. We observed no increase in tumor growth after lung injury in MIF knockout mice. We induced lung-specific overexpression of MIF in a double-transgenic mouse, and observed that MIF overexpression by itself was sufficient to accelerate the growth of orthotopic Lewis lung carcinoma tumors.

conclusionsLung injury leads to increased expression of the cytokine MIF, which results in protection from apoptosis and increased proliferation in orthotopic tumors injected after the acute phase of injury.

Indexed as

AnimalsApoptosisCarcinoma, Lewis LungCell ProliferationChronic DiseaseCytokinesDisease Models, AnimalImmunohistochemistryLung InjuryLung NeoplasmsMacrophage Migration-Inhibitory FactorsMiceMice, Inbred C57BLMice, KnockoutNeovascularization, PathologicTumor Cells, CulturedCytokinesMacrophage Migration-Inhibitory Factors

Identifiers

PMID20581170
PMCPMC2970845
OpenAlexW2041631102

What OpenQuestion holds

Textmetadata
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.