Evidence map›Paper›PMID 22036805›Full record

ArticleCellular signalling2012

The putative tumor suppressor Zc3h12d modulates toll-like receptor signaling in macrophages.

Shengping Huang, Dongfei Qi, Jian Liang, Ruidong Miao, Kentaro Minagawa, Tim Quinn, Toshimitsu Matsui, Daping Fan, Jianguo Liu, Mingui Fu

Open access · greenAbstract read
In one paragraph

Article in Cellular signalling, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

38 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Macrophage Zc3h12c Limits Tissue Inflammation and Injury via Alternative Splicing of Pre-mRNA.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. ZC3H12D upregulation in head and neck squamous cell carcinoma: a potential prognostic biomarker associated with immune infiltration.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2025
    Article
  10. The homeostatic function of Regnase-2 restricts neuroinflammation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  11. Frontiers in immunology · 2023
    Article
  12. Review
  13. Article
  14. Article
  15. Article
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  17. 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

10 authors at 5 institutions in 2 countries.

Shengping HuangShock/Trauma Research Center & Department of Basic Medical Science, School of Medicine, University of Missouri Kansas City, MO 64108, United States.
Dongfei QiShock/Trauma Research Center & Department of Basic Medical Science, School of Medicine, University of Missouri Kansas City, MO 64108, United States.
Jian LiangBurnett School of Biological Science, College of Medicine, University of Central Florida, Orlando, FL 32816, United States.
Ruidong MiaoShock/Trauma Research Center & Department of Basic Medical Science, School of Medicine, University of Missouri Kansas City, MO 64108, United States.
Kentaro MinagawaKobe University Graduate School of Medicine, Kobe, Japan.
Tim QuinnShock/Trauma Research Center & Department of Basic Medical Science, School of Medicine, University of Missouri Kansas City, MO 64108, United States.
Toshimitsu MatsuiKobe University Graduate School of Medicine, Kobe, Japan.
Daping FanDepartment of Cell Biology and Anatomy, University of South Carolina, Columbia, SC 29209, United States.
Jianguo LiuDepartment of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO 63104, United States.
Mingui FuShock/Trauma Research Center & Department of Basic Medical Science, School of Medicine, University of Missouri Kansas City, MO 64108, United States. Electronic address: fum@umkc.edu.
University of Missouri–Kansas City · USKobe University · JPSaint Louis University · USUniversity of Central Florida · USUniversity of South Carolina · US

Funding

UBIQUITIN CARBOXYL TERMINAL HYDROLASE L1 (UCH-L1) AND VASCULAR LESION FORMATIONP20RR016434 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MARKWALD, ROGER R · 2001 to 2011
$24.8M
SOUTH CAROLINA CLINICAL & TRANSLATIONAL RESEARCH INSTITUTE (SCTR)UL1RR029882 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T. · 2009 to 2011
$10.1M
South Carolina Clinical & Translational Research Institute (SCTR)UL1TR000062 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T. · 2012 to 2014
$9.4M
Molecular mechanisms of host-derived CCL5 mediated mammary tumor growthK22CA137126 · NCI · SAINT LOUIS UNIVERSITY · PI LIU, JIANGUO · 2010 to 2012
$515k
The role of MCPIP1 in regulating NF-kB signaling and macrophage activationR21HL098794 · NHLBI · UNIVERSITY OF MISSOURI KANSAS CITY · PI FU, MINGUI · 2011 to 2012
$413k
Monocyte microRNA155 and atherosclerosisR21HL106325 · NHLBI · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI FAN, DAPING · 2011 to 2012
$377k
PARP-1 in Juvenile Idiopathic Arthritis-associated IL-10 Promoter PolymorphismsR03AR055353 · NIAMS · SAINT LOUIS UNIVERSITY · PI LIU, JIANGUO · 2009 to 2011
$218k
NCATS NIH HHS UL1 TR000062NCI NIH HHS CA-137126NCI NIH HHS K22 CA137126NCRR NIH HHS P20 RR016434NCRR NIH HHS RR-016434NCRR NIH HHS UL1 RR029882NHLBI NIH HHS HL-098794NHLBI NIH HHS HL-106325NHLBI NIH HHS R21 HL098794NHLBI NIH HHS R21 HL106325NIAMS NIH HHS AR-055353NIAMS NIH HHS R03 AR055353
6 · The paper itself

Abstract

Toll-like receptors (TLR) are pivotal in macrophage activation. The molecular mechanisms controlling TLR signaling and macrophage activation are not completely understood. Zc3h12d is originally identified as a possible tumor suppressor gene. However, its function remains unknown. We here report that Zc3h12d negatively regulates TLR signaling and macrophage activation. Zc3h12d was enriched in spleen, lung and lymph node. In macrophages, the expression of Zc3h12d was remarkably induced by TLR ligands through JNK and NF-κB signal pathways. On the other hand, overexpression of Zc3h12d significantly inhibited TLR2 and TLR4 activation-induced JNK, ERK and NF-κB signaling as well as macrophage inflammation. Similar to Zc3h12a/MCPIP1, Zc3h12d also decreased the global cellular protein ubiquitination. These findings suggest that Zc3h12d is a novel negative feedback regulator of TLR signaling and macrophage activation and thus may play a role in host immunity and inflammatory diseases.

Indexed as

Feedback, PhysiologicalImmunity, InnateAnimalsCell Cycle ProteinsEndonucleasesEndoribonucleasesExtracellular Signal-Regulated MAP KinasesGene ExpressionHEK293 CellsHumansInflammationMacrophage ActivationMacrophagesMaleMAP Kinase Kinase 4MiceCell Cycle ProteinsEndonucleasesEndoribonucleasesExtracellular Signal-Regulated MAP KinasesMAP Kinase Kinase 4NF-kappa BProteinsToll-Like Receptor 2Toll-Like Receptor 4Tumor Suppressor ProteinsZC3H12D protein, humanZc3h12d protein, mouse

Identifiers

PMID22036805
PMCPMC3237786
OpenAlexW2025533598

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.