Evidence map›Paper›PMID 39468452›Full record

ArticleCellular & molecular biology letters2024

Transactivation of the EGF receptor as a novel desensitization mechanism for G protein-coupled receptors, illustrated by dopamine D2-like and β

Dooti Kundu, Xiao Min, Shujie Wang, Lulu Peng, Xinru Tian, Mengling Wang, Kyeong-Man Kim

Abstract read
In one paragraph

Article in Cellular & molecular biology letters, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

7 authors.

Dooti KunduDepartment of Pharmacology, College of Pharmacy, Chonnam National University, Gwang-Ju, 61186, Korea.
Xiao MinDepartment of Pharmacology, College of Pharmacy, Chonnam National University, Gwang-Ju, 61186, Korea.
Shujie WangDepartment of Pharmacology, College of Pharmacy, Chonnam National University, Gwang-Ju, 61186, Korea.
Lulu PengDepartment of Pharmacology, College of Pharmacy, Chonnam National University, Gwang-Ju, 61186, Korea.
Xinru TianDepartment of Pharmacology, College of Pharmacy, Chonnam National University, Gwang-Ju, 61186, Korea.
Mengling WangDepartment of Pharmacology, College of Pharmacy, Chonnam National University, Gwang-Ju, 61186, Korea.
Kyeong-Man KimDepartment of Pharmacology, College of Pharmacy, Chonnam National University, Gwang-Ju, 61186, Korea. kmkim@jnu.ac.kr.ORCID http://orcid.org/0000-0002-8138-4135

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transactivation of epidermal growth factor receptors (EGFR) provides intricate control over multiple regulatory cellular processes that merge the diversity of G protein-coupled receptors (GPCRs) with the robust signaling capacities of receptor tyrosine kinases. Contrary to the typical assertions, our findings demonstrate that EGFR transactivation contributes to the desensitization of GPCRs. Repeated agonist stimulation of certain GPCRs enhanced EGFR transactivation, triggering a series of cellular events associated with GPCR desensitization. This effect was observed in receptors undergoing desensitization (D

Indexed as

ErbB ReceptorsReceptors, Adrenergic, beta-2Receptors, Dopamine D2Transcriptional ActivationEpidermal Growth FactorG-Protein-Coupled Receptor Kinase 2G-Protein-Coupled Receptor KinasesHEK293 CellsHumansPhosphorylationQuinazolinesSignal TransductionTyrphostinsEpidermal Growth FactorErbB ReceptorsG-Protein-Coupled Receptor Kinase 2G-protein-coupled receptor kinase 6G-Protein-Coupled Receptor KinasesGRK2 protein, humanQuinazolinesReceptors, Adrenergic, beta-2Receptors, Dopamine D2RTKI cpdTyrphostinsArrestinDesensitizationDeubiquitinationEGFRGPCRTransactivation

Identifiers

PMID39468452
PMCPMC11514929

What OpenQuestion holds

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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.