Evidence map›Paper›PMID 22461508›Full record

ArticleCancer research2012

MIF produced by bone marrow-derived macrophages contributes to teratoma progression after embryonic stem cell transplantation.

Xi Wang, Tianxiang Chen, Lin Leng, Jianqing Fan, Kai Cao, Zhaoxia Duan, Xijing Zhang, Changshun Shao, Mingmei Wu, Iman Tadmori and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

29 citing papers in PubMed, 48 citations in OpenAlex.

  1. Systematic and precise interventions for KRAS-mutant cancers.Experimental hematology & oncology · 2026
    Review
  2. Article
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  10. MIF-Dependent Control of Tumor Immunity.Frontiers in immunology · 2020
    Review
  11. Article
  12. Article
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  15. Article
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  17. Macrophage Migration Inhibitory Factor Mediates Proliferative GN via CD74.Journal of the American Society of Nephrology : JASN · 2016
    Article
  18. Article
  19. Article
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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

18 authors at 10 institutions in 3 countries.

Xi WangW. M. Keck Center for Collaborative Neuroscience, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA.
Tianxiang Chen
Lin Leng
Jianqing Fan
Kai Cao
Zhaoxia Duan
Xijing Zhang
Changshun Shao
Mingmei Wu
Iman Tadmori
Tianyi Li
Li Liang
Dongming Sun
Shusen Zheng
Andreas Meinhardt
Wise Young
Richard Bucala
Yi Ren
Air Force Medical University · CNArmy Medical University · CNFirst Affiliated Hospital Zhejiang University · CNRutgers, The State University of New Jersey · USUniversity of Giessen · DEYale University · USDaping Hospital · CNPrinceton University · USXijing Hospital · CNZhejiang University · CN

Funding

MIF AND THE HOST RESPONSE TO INFECTIONR01AI042310 · NIAID · YALE UNIVERSITY · PI BUCALA, RICHARD J · 1998 to 2013
$4.3M
Statistical Methods for Ultrahigh-dimensional Biomedical DataR01GM072611 · NIGMS · PRINCETON UNIVERSITY · PI CATTANEO, MATIAS DAMIAN · 2006 to 2021
$4.2M
Quantitative Methods for Genome-wide Analysis of Macrophage Activation by ESCsR01GM100474 · NIGMS · PRINCETON UNIVERSITY · PI FAN, JIANQING · 2011 to 2014
$1.5M
MIF and Host Response to InfectionR56AI042310 · NIAID · YALE UNIVERSITY · PI BUCALA, RICHARD J · 2014 to 2014
$426k
NIAID NIH HHS R01 AI042310NIAID NIH HHS R56 AI042310NIGMS NIH HHS R01 GM072611NIGMS NIH HHS R01 GM100474-01
6 · The paper itself

Abstract

Although stem cell therapy holds promise as a potential treatment in a number of diseases, the tumorigenicity of embryonic stem cells (ESC) and induced pluripotent stem cells remains a major obstacle. In vitro predifferentiation of ESCs can help prevent the risk of teratoma formation, yet proliferating neural progenitors can generate tumors, especially in the presence of immunosuppressive therapy. In this study, we investigated the effects of the microenvironment on stem cell growth and teratoma development using undifferentiated ESCs. Syngeneic ESC transplantation triggered an inflammatory response that involved the recruitment of bone marrow (BM)-derived macrophages. These macrophages differentiated into an M2 or angiogenic phenotype that expressed multiple angiogenic growth factors and proteinases, such as macrophage migration inhibitory factor (MIF), VEGF, and matrix metalloproteinase 9, creating a microenvironment that supported the initiation of teratoma development. Genetic deletion of MIF from the host but not from ESCs specifically reduced angiogenesis and teratoma growth, and MIF inhibition effectively reduced teratoma development after ESC transplantation. Together, our findings show that syngeneic ESC transplantation provokes an inflammatory response that involves the rapid recruitment and activation of BM-derived macrophages, which may be a crucial driving force in the initiation and progression of teratomas.

Indexed as

AnimalsCell DifferentiationCell MovementDisease ProgressionEmbryonic Stem CellsEndothelial CellsIntramolecular OxidoreductasesMacrophage ActivationMacrophage Migration-Inhibitory FactorsMacrophagesMiceMice, Inbred C57BLMice, KnockoutNeovascularization, PathologicStem Cell NicheStem Cell TransplantationIntramolecular OxidoreductasesMacrophage Migration-Inhibitory FactorsMif protein, mouse

Identifiers

PMID22461508
PMCPMC3779606
OpenAlexW2115984648

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.