Evidence map›Paper›PMID 27326393›Full record

ArticleTranslational medicine @ UniSa2016

Dual role of GRK5 in cancer development and progression.

J Gambardella, A Franco, C Del Giudice, A Fiordelisi, E Cipolletta, M Ciccarelli, B Trimarco, G Iaccarino, D Sorriento

Open access · greenAbstract read
In one paragraph

Article in Translational medicine @ UniSa, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Targeting GRK5 for Treating Chronic Degenerative Diseases.International journal of molecular sciences · 2021
    Review
  7. Article
  8. Article
  9. Article
  10. G Protein-Coupled Receptor Systems and Their Role in Cellular Senescence.Computational and structural biotechnology journal · 2019
    Review
  11. Article
  12. Review
  13. A Novel Small Peptide Inhibitor of NFOxidative medicine and cellular longevity · 2018
    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

9 authors at 1 institution in 1 country.

J GambardellaDepartment of Medicine and Surgery -University of Salerno, Italy;
A FrancoDepartment of Advanced Biomedical Science -"Federico II" University of Naples, Italy;
C Del GiudiceDepartment of Advanced Biomedical Science -"Federico II" University of Naples, Italy;
A FiordelisiDepartment of Advanced Biomedical Science -"Federico II" University of Naples, Italy;
E CipollettaDepartment of Medicine and Surgery -University of Salerno, Italy;
M CiccarelliDepartment of Medicine and Surgery -University of Salerno, Italy;
B TrimarcoDepartment of Advanced Biomedical Science -"Federico II" University of Naples, Italy;
G IaccarinoDepartment of Medicine and Surgery -University of Salerno, Italy;
D SorrientoInstitute of Biostructure and Bioimaging - CNR, Naples, Italy.
University of Salerno · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GRK5 is a multifunctional protein that is able to move within the cell in response to various stimuli to regulate key intracellular signaling from receptor activation, on plasmamembrane, to gene transcription, in the nucleus. Thus, GRK5 is involved in the development and progression of several pathological conditions including cancer. Several reports underline the involvement of GRK5 in the regulation of tumor growth even if they appear controversial. Indeed, depending on its subcellular localization and on the type of cancer, GRK5 is able to both inhibit cancer progression, through the desensitization of GPCR and non GPCR-receptors (TSH, PGE2R, PDGFR), and induce tumor growth, acting on non-receptor substrates (p53, AUKA and NPM1). All these findings suggest that targeting GRK5 could be an useful anti-cancer strategy, for specific tumor types. In this review, we will discuss the different effects of this kinase in the induction and progression of tumorigenesis, the molecular mechanisms by which GRK5 exerts its effects, and the potential therapeutic strategies to modulate them.

Indexed as

cancerGPCRGRK5

Identifiers

PMID27326393
PMCPMC4912336
OpenAlexW2483840530

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.