Evidence map›Paper›PMID 29483837›Full record

ReviewInternational journal of biological sciences2018

The Role of G Protein-coupled Receptor Kinases in Cancer.

Shan Yu, Litao Sun, Yufei Jiao, Leo Tsz On Lee

Open access · goldAbstract readReview
In one paragraph

Review in International journal of biological sciences, 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
3.2field-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

39 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. GPCR Biased Signaling in Cancer.Handbook of experimental pharmacology · 2026
    Review
  5. Discovery ofActa pharmaceutica Sinica. B · 2025
    Article
  6. Article
  7. Article
  8. Article
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  11. Review
  12. Article
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  16. Article
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  18. Review
  19. The LPAInternational journal of molecular sciences · 2021
    Review
  20. Review
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 2 institutions in 2 countries.

Shan YuCentre of Reproduction Development and Aging, Faculty of Health Sciences, University of Macau, Taipa, Macau.
Litao SunDepartment of Ultrasound, The Secondary Affiliated Hospital of Harbin Medical University, Harbin, China.
Yufei JiaoDepartment of Pathology, The Secondary Affiliated Hospital of Harbin Medical University, Harbin, China.
Leo Tsz On LeeCentre of Reproduction Development and Aging, Faculty of Health Sciences, University of Macau, Taipa, Macau.
Second Affiliated Hospital of Harbin Medical University · CNUniversity of Macau · MO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) are the largest family of plasma membrane receptors. Emerging evidence demonstrates that signaling through GPCRs affects numerous aspects of cancer biology such as vascular remolding, invasion, and migration. Therefore, development of GPCR-targeted drugs could provide a new therapeutic strategy to treating a variety of cancers. G protein-coupled receptor kinases (GRKs) modulate GPCR signaling by interacting with the ligand-activated GPCR and phosphorylating its intracellular domain. This phosphorylation initiates receptor desensitization and internalization, which inhibits downstream signaling pathways related to cancer progression. GRKs can also regulate non-GPCR substrates, resulting in the modulation of a different set of pathophysiological pathways. In this review, we will discuss the role of GRKs in modulating cell signaling and cancer progression, as well as the therapeutic potential of targeting GRKs.

Indexed as

AnimalsCell CommunicationCell Line, TumorDisease ProgressionG-Protein-Coupled Receptor KinasesHumansNeoplasmsPhosphorylationProtein DomainsProtein Kinase InhibitorsSignal TransductionG-Protein-Coupled Receptor KinasesProtein Kinase InhibitorsCancerCell signalingG protein-coupled receptor (GPCR)G protein-coupled receptor kinase (GRK)

Identifiers

PMID29483837
PMCPMC5821040
OpenAlexW2789677243

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.