Evidence map›Paper›PMID 36214539›Full record

ArticleThe Journal of pathology2023

Role of MIF1/MIF2/CD74 interactions in bladder cancer.

Benjamin L Woolbright, Ganeshkumar Rajendran, Erika Abbott, Austin Martin, Sarah Amalraj, Katie Dennis, Xiaogang Li, Joshua Warrick, John A Taylor

Open access · greenAbstract read
In one paragraph

Article in The Journal of pathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. International journal of surgery (London, England) · 2026
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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 4 institutions in 1 country.

Benjamin L WoolbrightDepartment of Urology, University of Kansas Medical Center, Kansas City, KS, USA.ORCID 0000-0003-3219-958X
Ganeshkumar RajendranDepartment of Urology, University of Kansas Medical Center, Kansas City, KS, USA.
Erika AbbottDepartment of Urology, University of Kansas Medical Center, Kansas City, KS, USA.
Austin MartinSchool of Medicine, Kansas University Medical Center, Kansas City, KS, USA.
Sarah AmalrajDepartment of Urology, University of Kansas Medical Center, Kansas City, KS, USA.
Katie DennisDepartment of Pathology, Kansas University Medical Center, Kansas City, KS, USA.
Xiaogang LiDepartment of Medicine, Mayo Clinic, Rochester, MN, USA.
Joshua WarrickDepartment of Pathology and Laboratory Medicine, The Pennsylvania State University, Hershey, PA, USA.
John A TaylorDepartment of Urology, University of Kansas Medical Center, Kansas City, KS, USA.
University of Kansas Medical Center · USUniversity Medical Center · USMayo Clinic in Arizona · USPennsylvania State University · US

Funding

Transgenic & Gene-Targeting Shared ResourceP30CA168524 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ROY A. JENSEN · 2012 to 2026
$40.1M
NCI NIH HHS P30 CA168524
6 · The paper itself

Abstract

Macrophage migration inhibitory factor (MIF1) is a pleiotropic cytokine involved in inflammation and cancer. Genetic knockout of Mif1 in the validated N-butyl-N-(4-hydroxybutyl) nitrosamine (BBN) model of bladder cancer (BCa) resulted in stage arrest at non-muscle-invasive disease in prior studies. Small-molecule inhibition of MIF1 reduced cancer-associated outcomes, but it did not fully recapitulate genetic models. D-dopachrome tautomerase (gene symbol DDT), commonly referred to as MIF2, is a functional homolog of MIF1, and both MIF1 and MIF2 can bind the cell surface receptor CD74 on multiple cell types to initiate a signaling cascade. It has been proposed that this interaction mediates part of the protumorigenic effects of MIF1 and MIF2 and may explain the discordance in prior studies. We hypothesized that MIF2 functions redundantly with MIF1 in BCa development and progression. The Cancer Genome Atlas (TCGA) analysis indicated MIF and DDT expression were increased in BCa patients compared to control. 4-Iodopyridine (4-IPP), a combined MIF1/MIF2 inhibitor, was more efficacious than ISO-1, a MIF1-only inhibitor, in preventing cellular proliferation in BCa cell lines. To evaluate these findings in vivo, wild-type (WT) and Mif1

Indexed as

Macrophage Migration-Inhibitory FactorsUrinary Bladder NeoplasmsAnimalsCell ProliferationDDTSignal TransductionDDTMacrophage Migration-Inhibitory Factorsbladder cancerd-dopachrome tautomerasemacrophage migration inhibitory factor

Identifiers

PMID36214539
PMCPMC10031641
OpenAlexW4304014798

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.