Evidence map›Paper›PMID 30984536›Full record

ArticleFEBS open bio2019

Hypermethylation of the G protein-coupled receptor kinase 6 (GRK6) promoter inhibits binding of C/EBPα, and GRK6 knockdown promotes cell migration and invasion in lung adenocarcinoma cells.

Sumei Yao, Dandan Wu, Jinliang Chen, Peng Wang, Xuedong Lv, Jianan Huang

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
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  6. Article
  7. Frontiers in oncology · 2021
    Article
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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

6 authors at 3 institutions in 1 country.

Sumei YaoDepartment of Respiratory the First Affiliated Hospital of Soochow University Suzhou China.
Dandan WuDepartment of Respiratory the Second Affiliated Hospital of Nantong University China.
Jinliang ChenDepartment of Respiratory the Second Affiliated Hospital of Nantong University China.
Peng WangDepartment of Respiratory the Second Affiliated Hospital of Nantong University China.
Xuedong LvDepartment of Respiratory the Second Affiliated Hospital of Nantong University China.
Jianan HuangDepartment of Respiratory the First Affiliated Hospital of Soochow University Suzhou China.
Second Affiliated Hospital of Nantong UniversityAffiliated Hospital of Nantong University · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously reported that the expression of G protein-coupled receptor kinase 6 (GRK6) is significantly downregulated in lung adenocarcinoma (LADC) tissues, and low expression levels of GRK6 are correlated with poor survival prognosis. However, the specific regulatory mechanisms and functions of GRK6 in LADC remain unknown. Here, we report that GRK6 mRNA expression levels are downregulated in LADC tissues compared to those in matched adjacent non-tumor tissues (

Indexed as

Promoter Regions, GeneticAdenocarcinoma of LungCCAAT-Enhancer-Binding ProteinsCell MovementDNA MethylationFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesG-Protein-Coupled Receptor KinasesHumansLung NeoplasmsMaleMiddle AgedNeoplastic ProcessesRNA, MessengerCCAAT-Enhancer-Binding ProteinsCEBPA protein, humanG-protein-coupled receptor kinase 6G-Protein-Coupled Receptor KinasesRNA, MessengerC/EBPαDNA methylationepigenetic regulationGRK6lung adenocarcinoma

Identifiers

PMID30984536
PMCPMC6443861
OpenAlexW2912640278

What OpenQuestion 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 OpenQuestion graph.