Evidence map›Paper›PMID 30158126›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2018

The Atypical Chemokine Receptor Ackr2 Constrains NK Cell Migratory Activity and Promotes Metastasis.

Christopher A H Hansell, Alasdair R Fraser, Alan J Hayes, Marieke Pingen, Claire L Burt, Kit Ming Lee, Laura Medina-Ruiz, Demi Brownlie, Megan K L Macleod, Paul Burgoyne and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
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  8. Chemoradiotherapy-induced ACKR2Cell reports. Medicine · 2024
    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

13 authors at 1 institution in 2 countries.

Christopher A H HansellChemokine Research Group, Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow G12 8TA, United Kingdom.
Alasdair R FraserChemokine Research Group, Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow G12 8TA, United Kingdom.
Alan J HayesChemokine Research Group, Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow G12 8TA, United Kingdom.ORCID 0000-0003-2708-6230
Marieke PingenChemokine Research Group, Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow G12 8TA, United Kingdom.ORCID 0000-0001-5689-9076
Claire L BurtChemokine Research Group, Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow G12 8TA, United Kingdom.ORCID 0000-0003-3544-7585
Kit Ming LeeChemokine Research Group, Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow G12 8TA, United Kingdom.ORCID 0000-0002-0475-3865
Laura Medina-RuizChemokine Research Group, Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow G12 8TA, United Kingdom.
Demi BrownlieChemokine Research Group, Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow G12 8TA, United Kingdom.ORCID 0000-0001-5932-6425
Megan K L MacleodChemokine Research Group, Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow G12 8TA, United Kingdom.ORCID 0000-0003-1843-8580
Paul BurgoyneChemokine Research Group, Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow G12 8TA, United Kingdom.
Gillian J WilsonChemokine Research Group, Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow G12 8TA, United Kingdom.ORCID 0000-0002-9513-8437
Robert J B NibbsChemokine Research Group, Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow G12 8TA, United Kingdom.ORCID 0000-0002-8150-0044
Gerard J GrahamChemokine Research Group, Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow G12 8TA, United Kingdom gerard.graham@glasgow.ac.uk chahansell@gmail.com.
Institute of Infection and Immunity · CA

Funding

Medical Research Council G0901113Medical Research Council MR/M019764/1Wellcome Trust 097821/Z/11/ZWellcome Trust 099251
6 · The paper itself

Abstract

Chemokines have been shown to be essential players in a range of cancer contexts. In this study, we demonstrate that mice deficient in the atypical chemokine receptor Ackr2 display impaired development of metastasis in vivo in both cell line and spontaneous models. Further analysis reveals that this relates to increased expression of the chemokine receptor CCR2, specifically by KLRG1

Indexed as

AnimalsCarcinoma, Lewis LungCell MovementChemokine CCL2Chemokine Receptor D6Cytotoxicity, ImmunologicKiller Cells, NaturalLectins, C-TypeMelanoma, ExperimentalMiceMice, Inbred C57BLMice, KnockoutNeoplasm MetastasisNeoplasms, ExperimentalReceptors, CCR2Receptors, ChemokineAckr2 protein, mouseCcr2 protein, mouseChemokine CCL2Chemokine Receptor D6Klrg1 protein, mouseLectins, C-TypeReceptors, CCR2Receptors, ChemokineReceptors, Immunologic

Identifiers

PMID30158126
PMCPMC6176105
OpenAlexW2889439413

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.