Evidence map›Paper›PMID 29903572›Full record

ReviewCytokine2018

Emerging roles of atypical chemokine receptor 3 (ACKR3) in normal development and physiology.

K E Quinn, D I Mackie, K M Caron

Abstract readReview
In one paragraph

Review in Cytokine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
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

39 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Regulation of the Hippo/YAP axis by CXCR7 in the tumorigenesis of gastric cancer.Journal of experimental & clinical cancer research : CR · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Role of G-protein coupled receptors in cardiovascular diseases.Frontiers in cardiovascular medicine · 2023
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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

3 authors.

K E QuinnDepartment of Cell Biology and Physiology, 111 MasonFarm Rd., 6312B MBRB CB# 7545, The University of North Carolina, Chapel Hill, NC 27599-7545, USA.
D I MackieDepartment of Cell Biology and Physiology, 111 MasonFarm Rd., 6312B MBRB CB# 7545, The University of North Carolina, Chapel Hill, NC 27599-7545, USA.
K M CaronDepartment of Cell Biology and Physiology, 111 MasonFarm Rd., 6312B MBRB CB# 7545, The University of North Carolina, Chapel Hill, NC 27599-7545, USA. Electronic address: kathleen_caron@med.unc.edu.

Funding

Adrenomedullin Signaling at the Maternal-Fetal InterfaceR01HD060860 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Kathleen M Caron · 2009 to 2026
$4.8M
Cardiac Lymphatics in Heart FailureR01HL129086 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CARON, KATHLEEN M · 2016 to 2023
$4.1M
Novel Interactions Between G protein coupled receptors and Receptor Activity Modifying Proteins and Their Control of Angiogenic CuesF32HL134279 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MACKIE, DUNCAN IAN · 2016 to 2018
$174k
NHLBI NIH HHS F32 HL134279NHLBI NIH HHS R01 HL129086NICHD NIH HHS R01 HD060860
6 · The paper itself

Abstract

The discovery that atypical chemokine receptors (ACKRs) can initiate alternative signaling pathways rather than classical G-protein coupled receptor (GPCR) signaling has changed the paradigm of chemokine receptors and their roles in modulating chemotactic responses. The ACKR family has grown over the years, with discovery of new functions and roles in a variety of pathophysiological conditions. However, the extent to which these receptors regulate normal physiology is still continuously expanding. In particular, atypical chemokine receptor 3 (ACKR3) has proven to be an important receptor in mediating normal biological functions, including cardiac development and migration of cortical neurons. In this review, we illustrate the versatile and intriguing role of ACKR3 in physiology.

Indexed as

AnimalsCell LineCell ProliferationChemokine CXCL11Chemokine CXCL12ChemotaxisEmbryo ImplantationFemaleHEK293 CellsHumansMaleMiceReceptors, CXCRSignal TransductionSpermatogenesisVasodilationACKR3 protein, humanChemokine CXCL11Chemokine CXCL12CXCL11 protein, humanCXCL12 protein, humanReceptors, CXCRAdrenomedullinAtypical chemokine receptor 3/chemokine receptor 7 (ACKR3/CXCR7)C-X-C motif chemokine ligand 11 (CXCL11)C-X-C motif chemokine ligand 12 (CXCL12)Physiology

Identifiers

PMID29903572
PMCPMC6005205

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.