Evidence map›Paper›PMID 36307250›Full record

ReviewTrends in pharmacological sciences2022

Atypical chemokine receptors: emerging therapeutic targets in cancer.

Robert J Torphy, Elliott J Yee, Richard D Schulick, Yuwen Zhu

Open access · greenAbstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.6field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  3. GPR182 is a lipoprotein receptor for dietary fat absorption.The Journal of clinical investigation · 2026
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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

4 authors at 1 institution in 1 country.

Robert J TorphyDepartment of Surgery, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Elliott J YeeDepartment of Surgery, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Richard D SchulickDepartment of Surgery, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Yuwen ZhuDepartment of Surgery, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA. Electronic address: yuwen.zhu@cuanschutz.edu.
University of Colorado Anschutz Medical Campus · US

Funding

NIH Prior Approval Process ProfessionalUL1TR002535 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2018 to 2022
$51.1M
The CD93 pathway and melanoma therapyR01CA258302 · NCI · UNIVERSITY OF COLORADO DENVER · PI Yuwen Zhu · 2022 to 2026
$1.8M
Melanoma Immunotherapy with GPR182 blockadeR01CA269644 · NCI · UNIVERSITY OF COLORADO DENVER · PI Yuwen Zhu · 2023 to 2026
$1.4M
The GPR171 pathway in cancer immunotherapyR01CA279398 · NCI · UNIVERSITY OF COLORADO DENVER · PI Yuwen Zhu · 2023 to 2026
$1.4M
NCATS NIH HHS UL1 TR002535NCI NIH HHS R01 CA258302NCI NIH HHS R01 CA269644NCI NIH HHS R01 CA279398
6 · The paper itself

Abstract

Atypical chemokine receptors (ACKRs) regulate the availability of chemokines via chemokine scavenging, while also having the capacity to elicit downstream function through β-arrestin coupling. This contrasts with conventional chemokine receptors that directly elicit immune cell migration through G protein-coupled signaling. The significance of ACKRs in cancer biology has previously been poorly understood, but recent findings have highlighted the multifaceted role of these receptors in tumorigenesis and immune response modulation within the tumor microenvironment (TME). Additionally, recent research has expanded our understanding of the function of several receptors including GPR182, CCRL2, GPR1, PITPNM3, and C5aR2 that share similarities with the ACKR family. In this review, we discuss these recent developments, and highlight the opportunities and challenges of pharmacologically targeting ACKRs in cancer.

Indexed as

NeoplasmsCarcinogenesisCell MovementChemokinesHumansSignal TransductionTumor MicroenvironmentChemokinesarrestin-coupled receptoratypical chemokine receptorcancerchemokineG protein-coupled receptorimmunotherapy

Identifiers

PMID36307250
PMCPMC9669249
OpenAlexW4307583648

What OpenQuestion holds

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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.