Evidence map›Paper›PMID 31099111›Full record

ArticleMolecular carcinogenesis2019

Interleukin-37 is highly expressed in regulatory T cells of melanoma patients and enhanced by melanoma cell secretome.

Douglas G Osborne, Joanne Domenico, Yuchun Luo, Anna L Reid, Carol Amato, Zili Zhai, Dexiang Gao, Melanie Ziman, Charles A Dinarello, William A Robinson and 1 more

Open access · greenAbstract read
In one paragraph

Article in Molecular carcinogenesis, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  5. Article
  6. Deregulated Expression ofInternational journal of molecular sciences · 2023
    Article
  7. Frontiers in immunology · 2023
    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

11 authors at 5 institutions in 2 countries.

Douglas G OsborneDepartment of Dermatology, University of Colorado AMC, Aurora, Colorado.
Joanne DomenicoDepartment of Dermatology, University of Colorado AMC, Aurora, Colorado.
Yuchun LuoDepartment of Dermatology, University of Colorado AMC, Aurora, Colorado.
Anna L ReidSchool of Medical Sciences, Edith Cowan University, Perth, Western Australia, Australia.
Carol AmatoDepartment of Medicine, University of Colorado AMC, Aurora, Colorado.
Zili ZhaiDepartment of Dermatology, University of Colorado AMC, Aurora, Colorado.
Dexiang GaoColorado School of Public Health, University of Colorado AMC, Aurora, Colorado.
Melanie ZimanSchool of Medical Sciences, Edith Cowan University, Perth, Western Australia, Australia.
Charles A DinarelloDepartment of Medicine, University of Colorado AMC, Aurora, Colorado.
William A RobinsonDepartment of Medicine, University of Colorado AMC, Aurora, Colorado.
Mayumi FujitaDepartment of Dermatology, University of Colorado AMC, Aurora, Colorado.
University of Colorado Denver · USColorado School of Public Health · USDenver VA Medical Center · USEdith Cowan University · AUUniversity of Western Australia · AU

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Transgenic and Gene Targeting CoreP30AR057212 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI HOGAN, CHRISTOPHER J · 2009 to 2018
$6.2M
Modulation of Inflammasome-mediated cytokine activation by EGCG in human melanomaR01CA197919 · NCI · UNIVERSITY OF COLORADO DENVER · PI FUJITA, MAYUMI · 2016 to 2020
$1.9M
Developing a protocol for profiling blood markers of melanomaR03CA125833 · NCI · UNIVERSITY OF COLORADO DENVER · PI FUJITA, MAYUMI · 2008 to 2009
$154k
Autoinflammation in Human MelanomaI01BX001228 · VA · VA EASTERN COLORADO HEALTH CARE SYSTEM · PI FUJITA, MAYUMI · 2012 to 2022
–
BLRD VA I01 BX001228NCI NIH HHS P30 CA046934NCI NIH HHS R01 CA197919NCI NIH HHS R03 CA125833NIAMS NIH HHS P30 AR057212
6 · The paper itself

Abstract

Immune suppression is one of the 10 hallmarks of cancer. Interleukin-37 (IL-37), a member of the IL-1 family, inhibits both innate and adaptive immunity, and has been shown to modulate immune responses in various disease conditions. Yet, IL-37 has rarely been investigated in cancer patients, and its biological role in cancer remains to be elucidated. In this study, we investigated the gene expression of IL-37 in age- and sex-matched blood samples of healthy individuals and melanoma patients, and demonstrated upregulation of IL-37 messenger RNA (mRNA) in the blood samples of melanoma patients. By further analyzing immune cell subsets responsible for the upregulated IL-37 expression, we discovered that IL-37 mRNA was highly expressed in T cells and granulocytes, with the highest expression in regulatory T (T

Indexed as

Biomarkers, TumorCells, CulturedFemaleHumansInterleukin-1MaleMelanomaRNA, MessengerT-Lymphocytes, RegulatoryTransforming Growth Factor betaUp-RegulationBiomarkers, TumorIL37 protein, humanInterleukin-1RNA, MessengerTransforming Growth Factor betabloodIL-37melanomasecretomeTreg cells

Identifiers

PMID31099111
PMCPMC6692223
OpenAlexW2946517941

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.