Evidence map›Paper›PMID 27382437›Full record

ArticleGenes & cancer2016

Epigenetically silenced GNG4 inhibits SDF1α/CXCR4 signaling in mesenchymal glioblastoma.

Jagriti Pal, Vikas Patil, Baisakhi Mondal, Sudhanshu Shukla, Alangar S Hegde, Arimappamagan Arivazhagan, Vani Santosh, Kumaravel Somasundaram

Open access · diamondAbstract read
In one paragraph

Article in Genes & cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

30 citing papers in PubMed, 48 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Jagriti PalDepartment of Microbiology and Cell Biology, Indian Institute of Science, Bangalore, India.
Vikas PatilDepartment of Microbiology and Cell Biology, Indian Institute of Science, Bangalore, India.
Baisakhi MondalDepartment of Microbiology and Cell Biology, Indian Institute of Science, Bangalore, India.
Sudhanshu ShuklaDepartment of Microbiology and Cell Biology, Indian Institute of Science, Bangalore, India.
Alangar S HegdeSri Satya Sai Institute of Higher Medical Sciences, Bangalore, India.
Arimappamagan ArivazhaganDepartments of Neuropathology and Neurosurgery, National Institute of Mental Health and Neuro Sciences, Bangalore, India.
Vani SantoshDepartments of Neuropathology and Neurosurgery, National Institute of Mental Health and Neuro Sciences, Bangalore, India.
Kumaravel SomasundaramDepartment of Microbiology and Cell Biology, Indian Institute of Science, Bangalore, India.
Indian Institute of Science Bangalore · INNational Institute of Mental Health and Neurosciences · INSri Sathya Sai Institute of Higher Medical Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The most common and aggressive form of primary brain tumor in adults is glioblastoma (GBM). From the global DNA methylation profiling study, previously published from our laboratory, we identified Guanine Nucleotide binding-protein Gamma subunit 4 (GNG4) to be one of the most hyper methylated and down regulated genes in GBM. GBM derived cell lines showed reduced GNG4 transcript levels, which could be reversed by methylation inhibitor treatment. Bisulphite sequencing confirmed the methylation status in glioblastoma tumor tissue and GBM derived cell lines. Overexpression of GNG4 was found to inhibit proliferation and colony formation of GBM cell lines and in vitro transformation of immortalized human astrocytes, thus suggesting a potential tumor suppressor role of GNG4 in GBM. Correlation of GNG4 transcript levels with that of all GPCRs from TCGA data revealed chemokine receptors as the potential target of GNG4. Furthermore, exogenous over expression of GNG4 inhibited SDF1α/CXCR4-dependent chemokine signaling as seen by reduced pERK and pJNK and GBM cell migration. The inhibitory association between GNG4 and SDF1α/CXCR4 was more evident in mesenchymal subtype of GBM. Thus, this study identifies GNG4 as an inhibitor of SDF1α/CXCR4-dependent signaling and emphasizes the significance of epigenetic inactivation of GNG4 in glioblastoma, especially in mesenchymal subtype.

Indexed as

chemokine receptorCXCR4DNA hyper methylationglioblastomaG-proteinG-protein-coupled receptorsguanine nucleotide binding-protein gamma subunit 4SDF1α

Identifiers

PMID27382437
PMCPMC4918951
OpenAlexW2475213762

What OpenQuestion holds

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Registered trials

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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.