Evidence map›Paper›PMID 28356386›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

The Granulocyte Progenitor Stage Is a Key Target of IRF8-Mediated Regulation of Myeloid-Derived Suppressor Cell Production.

Colleen S Netherby, Michelle N Messmer, Lauren Burkard-Mandel, Sean Colligan, Austin Miller, Eduardo Cortes Gomez, Jianmin Wang, Michael J Nemeth, Scott I Abrams

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

58 citing papers in PubMed, 77 citations in OpenAlex.

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  8. [Myeloid-derived suppressor cells as important factors and potential targets for breast cancer progression].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2024
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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 1 institution in 1 country.

Colleen S NetherbyDepartment of Immunology, Roswell Park Cancer Institute, Buffalo, NY 14263.
Michelle N MessmerDepartment of Immunology, Roswell Park Cancer Institute, Buffalo, NY 14263.
Lauren Burkard-MandelDepartment of Immunology, Roswell Park Cancer Institute, Buffalo, NY 14263.
Sean ColliganDepartment of Immunology, Roswell Park Cancer Institute, Buffalo, NY 14263.
Austin MillerDepartment of Biostatistics and Bioinformatics, Roswell Park Cancer Institute, Buffalo, NY 14263; and.ORCID 0000-0001-9739-8462
Eduardo Cortes GomezDepartment of Biostatistics and Bioinformatics, Roswell Park Cancer Institute, Buffalo, NY 14263; and.
Jianmin WangDepartment of Biostatistics and Bioinformatics, Roswell Park Cancer Institute, Buffalo, NY 14263; and.
Michael J NemethDepartment of Immunology, Roswell Park Cancer Institute, Buffalo, NY 14263.
Scott I AbramsDepartment of Immunology, Roswell Park Cancer Institute, Buffalo, NY 14263; scott.abrams@roswellpark.org.ORCID 0000-0002-0966-6488
Roswell Park Comprehensive Cancer Center · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
MULTIDISCIPLINARY APPROACHES TUMOR IMMUNOLOGYT32CA085183 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI Scott I. Abrams · 2001 to 2026
$3.1M
Mechanisms Underlying Functional Programs of Tumor-Associated MacrophagesR01CA172105 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI ABRAMS, SCOTT I. · 2015 to 2019
$2.0M
IRF-8 as a Negative Regulator of CD11b+Gr-1+ Myeloid Cell Production and FunctionR01CA140622 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI ABRAMS, SCOTT I. · 2011 to 2015
$2.0M
Mechanisms of Macrophage-Mediated Tumor MetastasisF30CA200133 · NCI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI BURKARD, LAUREN E · 2015 to 2018
$135k
NCI NIH HHS F30 CA200133NCI NIH HHS P30 CA016056NCI NIH HHS R01 CA140622NCI NIH HHS R01 CA172105NCI NIH HHS T32 CA085183
6 · The paper itself

Abstract

Alterations in myelopoiesis are common across various tumor types, resulting in immature populations termed myeloid-derived suppressor cells (MDSCs). MDSC burden correlates with poorer clinical outcomes, credited to their ability to suppress antitumor immunity. MDSCs consist of two major subsets, monocytic and polymorphonuclear (PMN). Intriguingly, the latter subset predominates in many patients and tumor models, although the mechanisms favoring PMN-MDSC responses remain poorly understood. Ordinarily, lineage-restricted transcription factors regulate myelopoiesis that collectively dictate cell fate. One integral player is IFN regulatory factor (IRF)-8, which promotes monocyte/dendritic cell differentiation while limiting granulocyte development. We recently showed that IRF8 inversely controls MDSC burden in tumor models, particularly the PMN-MDSC subset. However, where IRF8 acts in the pathway of myeloid differentiation to influence PMN-MDSC production has remained unknown. In this study, we showed that: 1) tumor growth was associated with a selective expansion of newly defined IRF8

Indexed as

MyelopoiesisAnimalsCell DifferentiationCell ProliferationFemaleGene Expression Regulation, NeoplasticGranulocyte Precursor CellsGranulocytesHematopoiesisHumansInterferon Regulatory Factor-8Interferon Regulatory FactorsMammary Neoplasms, ExperimentalMiceMonocytesMyeloid CellsInterferon Regulatory Factor-8Interferon Regulatory Factors

Identifiers

PMID28356386
PMCPMC5450940
OpenAlexW2612857912

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.