Evidence map›Paper›PMID 28637666›Full record

ArticleBlood2017

NR4A orphan nuclear receptor family members, NR4A2 and NR4A3, regulate neutrophil number and survival.

Lynne R Prince, Svenja D Prosseda, Kathryn Higgins, Jennifer Carlring, Elizabeth C Prestwich, Nikolay V Ogryzko, Atiqur Rahman, Alexander Basran, Francesco Falciani, Philip Taylor and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 74 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Functional and Genetic Insights into the Role of theAnimals : an open access journal from MDPI · 2025
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  17. Neutrophils Culture in Collagen Gel System.Frontiers in immunology · 2022
    Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 2 countries.

Lynne R PrinceDepartment of Infection, Immunity and Cardiovascular Disease and.
Svenja D ProssedaDepartment of Infection, Immunity and Cardiovascular Disease and.
Kathryn HigginsDepartment of Infection, Immunity and Cardiovascular Disease and.
Jennifer CarlringDepartment of Infection, Immunity and Cardiovascular Disease and.
Elizabeth C PrestwichDepartment of Infection, Immunity and Cardiovascular Disease and.
Nikolay V OgryzkoBateson Centre, University of Sheffield, Sheffield, United Kingdom.
Atiqur RahmanDepartment of Infection, Immunity and Cardiovascular Disease and.
Alexander BasranDepartment of Infection, Immunity and Cardiovascular Disease and.
Francesco FalcianiInstitute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom.
Philip TaylorInstitute of Infection and Immunity, Cardiff University, Cardiff, United Kingdom; and.
Stephen A RenshawDepartment of Infection, Immunity and Cardiovascular Disease and.
Moira K B WhyteMRC Centre for Inflammation Research, Queen's Medical Institute, University of Edinburgh, Edinburgh, United Kingdom.
Ian SabroeDepartment of Infection, Immunity and Cardiovascular Disease and.
Immunité et Cancer · FRCardiff University · GBUniversity of Edinburgh · GBUniversity of Liverpool · GBUniversity of Sheffield · GB

Funding

Medical Research Council G0701932Medical Research Council G0801983Medical Research Council MR/K006312/1Medical Research Council MR/M004864/1
6 · The paper itself

Abstract

The lifespan of neutrophils is plastic and highly responsive to factors that regulate cellular survival. Defects in neutrophil number and survival are common to both hematologic disorders and chronic inflammatory diseases. At sites of inflammation, neutrophils respond to multiple signals that activate protein kinase A (PKA) signaling, which positively regulates neutrophil survival. The aim of this study was to define transcriptional responses to PKA activation and to delineate the roles of these factors in neutrophil function and survival. In human neutrophil gene array studies, we show that PKA activation upregulates a significant number of apoptosis-related genes, the most highly regulated of these being

Indexed as

AnimalsCell CountCell ProliferationCell SurvivalCyclic AMP-Dependent Protein KinasesDinoprostoneEnzyme ActivationGene DeletionGene Knockdown TechniquesHumansInflammationLarvaMiceMultigene FamilyNeutrophilsNuclear Receptor Subfamily 4, Group A, Member 2Cyclic AMP-Dependent Protein KinasesDinoprostoneNuclear Receptor Subfamily 4, Group A, Member 2Nuclear Receptor Subfamily 4, Group A, Member 3RNA, MessengerRNA, Small Interfering

Identifiers

PMID28637666
PMCPMC5570679
OpenAlexW2675382611

What OpenQuestion holds

Textmetadata
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.