Evidence map›Paper›PMID 25511108›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2015

Esophageal cancer-related gene-4 (ECRG4) interactions with the innate immunity receptor complex.

Sonia Podvin, Xitong Dang, Morgan Meads, Arwa Kurabi, Todd Costantini, Brian P Eliceiri, Andrew Baird, Raul Coimbra

Open access · greenAbstract read
In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

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  14. The Orphan C2orf40 Gene is a Neuroimmune Factor in Alzheimer's Disease.JSM Alzheimer's disease and related dementia · 2016
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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

8 authors at 1 institution in 1 country.

Sonia PodvinDivision of Trauma, Surgical Critical Care, Burns, and Acute Care Surgery, Department of Surgery, University of California, San Diego, San Diego, CA, USA.
Xitong Dang
Morgan Meads
Arwa Kurabi
Todd Costantini
Brian P Eliceiri
Andrew Baird
Raul Coimbra
University of California, San Diego · US

Funding

Role of Src family kinases in endothelial cell biologyR01HL073396 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELICEIRI, BRIAN P · 2002 to 2011
$3.5M
A Combinatorial Approach to Wound Healing for Protein, Gene and Cell TherapeuticsP20GM078421 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BAIRD, ANDREW · 2006 to 2009
$3.4M
Vascular mechanisms regulating breast cancer brain metastasisR01CA170140 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELICEIRI, BRIAN P, FELDING, BRUNIE H. · 2012 to 2016
$1.8M
Targeting the choroid plexus for drug translocation into CSFR21EY018479 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BAIRD, ANDREW · 2007 to 2010
$606k
Functional Selection of Novel Ligands from the Neuroendocrine SecretomeR43DK085871 · NIDDK · MANDALA BIOSCIENCES, LLC · PI LAROCCA, DANA · 2010 to 2010
$239k
NCI NIH HHS R01 CA170140NEI NIH HHS EY018479NEI NIH HHS R21 EY018479NHLBI NIH HHS HL73396NHLBI NIH HHS R01 HL073396NIDDK NIH HHS DK085871NIDDK NIH HHS R43 DK085871NIGMS NIH HHS P20 GM078421NIGMS NIH HHS P20-GM078421
6 · The paper itself

Abstract

OBJECTIVE AND

designThe human c2orf40 gene encodes a tumor suppressor gene called esophageal cancer-related gene-4 (ECRG4) with pro- and anti-inflammatory activities that depend on cell surface processing. Here, we investigated its physical and functional association with the innate immunity receptor complex.

methodsInteractions between ECRG4 and the innate immunity receptor complex were assessed by flow cytometry, immunohistochemistry, confocal microscopy, and co-immunoprecipitation. Phage display was used for ligand targeting to cells that overexpress the TLR4-MD2-CD14.

resultsImmunoprecipitation and immunohistochemical studies demonstrate a physical interaction between ECRG4 and TLR4-MD2-CD14 on human granulocytes. Flow cytometry shows ECRG4 on the cell surface of a subset of CD14(+) and CD16(+) leukocytes. In a cohort of trauma patients, the C-terminal 16 amino acid domain of ECRG4 (ECRG4(133-148)) appears to be processed and shed, presumably at a thrombin-like consensus sequence. Phage targeting this putative ligand shows that this peptide sequence internalizes into cells through the TLR4/CD14/MD2 complex, but modulates inflammation through non-canonical, NFκB signal transduction.

conclusionsECRG4 is present on the surface of human monocytes and granulocytes. Its interaction with the human innate immunity receptor complex supports a role for cell surface activation of ECRG4 during inflammation and implicates this receptor in its mechanism of action.

Indexed as

AdultFemaleGranulocytesHEK293 CellsHumansImmunity, InnateLipopolysaccharide ReceptorsLymphocyte Antigen 96MaleMiddle AgedMonocytesNeoplasm ProteinsToll-Like Receptor 4Tumor Suppressor ProteinsYoung AdultECRG4 protein, humanLipopolysaccharide ReceptorsLY96 protein, humanLymphocyte Antigen 96Neoplasm ProteinsTLR4 protein, humanToll-Like Receptor 4Tumor Suppressor Proteins

Identifiers

PMID25511108
PMCPMC4301958
OpenAlexW2069947286

What OpenQuestion holds

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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.