Evidence map›Paper›PMID 30885209›Full record

ArticleCell communication and signaling : CCS2019

NF-κB upregulates glutamine-fructose-6-phosphate transaminase 2 to promote migration in non-small cell lung cancer.

Szymon J Szymura, Jacob P Zaemes, David F Allison, Sheena H Clift, Jaclyn M D'Innocenzi, Lisa G Gray, Brian D McKenna, Benjamin B Morris, Stefan Bekiranov, Robin D LeGallo and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

35 citing papers in PubMed, 63 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

12 authors at 2 institutions in 1 country.

Szymon J SzymuraDepartment of Biochemistry & Molecular Genetics, University of Virginia, P.O. Box 800733, Charlottesville, VA, 22908, USA.
Jacob P ZaemesDepartment of Biochemistry & Molecular Genetics, University of Virginia, P.O. Box 800733, Charlottesville, VA, 22908, USA.
David F AllisonDepartment of Biochemistry & Molecular Genetics, University of Virginia, P.O. Box 800733, Charlottesville, VA, 22908, USA.
Sheena H CliftDepartment of Biochemistry & Molecular Genetics, University of Virginia, P.O. Box 800733, Charlottesville, VA, 22908, USA.
Jaclyn M D'InnocenziDepartment of Biochemistry & Molecular Genetics, University of Virginia, P.O. Box 800733, Charlottesville, VA, 22908, USA.
Lisa G GrayDepartment of Biochemistry & Molecular Genetics, University of Virginia, P.O. Box 800733, Charlottesville, VA, 22908, USA.
Brian D McKennaDepartment of Biochemistry & Molecular Genetics, University of Virginia, P.O. Box 800733, Charlottesville, VA, 22908, USA.
Benjamin B MorrisDepartment of Biochemistry & Molecular Genetics, University of Virginia, P.O. Box 800733, Charlottesville, VA, 22908, USA.
Stefan BekiranovDepartment of Biochemistry & Molecular Genetics, University of Virginia, P.O. Box 800733, Charlottesville, VA, 22908, USA.
Robin D LeGalloDepartment of Pathology, University of Virginia, P.O. Box 800733, Charlottesville, VA, 22908, USA.
David R JonesProfessor & Chief, Thoracic Surgery Service, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, Box 7, New York, NY, 10065, USA.
Marty W MayoDepartment of Biochemistry & Molecular Genetics, University of Virginia, P.O. Box 800733, Charlottesville, VA, 22908, USA. mwm3y@virginia.edu.ORCID 0000-0001-9443-5926
University of Virginia · USMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Translational Control in the Hepatitis C VirusS06GM008136 · NIGMS · NEW MEXICO STATE UNIVERSITY LAS CRUCES · PI KUEHN, GLENN D · 1989 to 2011
$23.2M
Cancer Research Training Program: From Molecular Mechanisms to Therapeutic StrategiesT32CA009109 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Andrew Carl Dudley, Melanie R Rutkowski · 1985 to 2026
$13.9M
BRMS1-mediated suppression of metastases in p53 mutant lung adenocarcinomaR01CA217169 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI JONES, DAVID R · 2018 to 2022
$2.5M
Role of IKK in NSCLC: Modulation of SMRT and NF-kappaBR01CA104397 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI MAYO, MARTY W · 2004 to 2012
$2.4M
Identifying tumor suppressor targets of SIRT6 in lung cancerR01CA192399 · NCI · UNIVERSITY OF VIRGINIA · PI MAYO, MARTY W · 2015 to 2019
$1.9M
Short-Term Training to Increase Diversity in Health-Related ResearchR25HL088724 · NHLBI · UNIVERSITY OF VIRGINIA · PI HALME, ADRIAN J, OWENS, GARY K · 2007 to 2022
$1.8M
Epigenetic and post-translational regulation of the metastasis suppressor BRMS1R01CA136705 · NCI · UNIVERSITY OF VIRGINIA · PI JONES, DAVID R · 2009 to 2013
$1.5M
Inflammatory Cytokines Link NF-kappaB with Bim Degradation and MetastasisR01CA132580 · NCI · UNIVERSITY OF VIRGINIA · PI MAYO, MARTY W · 2008 to 2012
$1.4M
KLF6: A driving factor of lung adenocarcinomaF32CA213898 · NCI · UNIVERSITY OF VIRGINIA · PI MCKENNA, BRIAN · 2017 to 2018
$87k
NCI NIH HHS F32 CA213898NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA104397NCI NIH HHS R01 CA132580NCI NIH HHS R01 CA136705NCI NIH HHS R01 CA192399NCI NIH HHS R01 CA217169NCI NIH HHS T32 CA009109NHLBI NIH HHS R25 HL088724NIGMS NIH HHS S06 GM008136
6 · The paper itself

Abstract

backgroundEpithelial-to-mesenchymal transition (EMT) results in changes that promote de-differentiation, migration, and invasion in non-small cell lung cancer (NSCLC). While it is recognized that EMT promotes altered energy utilization, identification of metabolic pathways that link EMT with cancer progression is needed. Work presented here indicates that mesenchymal NSCLC upregulates glutamine-fructose-6-phosphate transaminase 2 (GFPT2). GFPT2 is the rate-limiting enzyme in the synthesis of uridine diphosphate N-acetylglucosamine (UDP-GlcNAc). UDP-GlcNAc is the obligate activator of O-linked N-acetylglucosamine transferase (OGT).

methodsAnalysis of our transcriptomic data indicates that GFPT2 is one of the most significantly upregulated metabolic genes in mesenchymal NSCLC. Ectopic GFPT2 expression, as well as gene silencing strategies were used to determine the importance of this metabolic enzyme in regulating EMT-driven processes of cell motility and invasion.

resultsOur work demonstrates that GFPT2 is transcriptionally upregulated by NF-κB and repressed by the NAD

conclusionsConsistent with GFPT2 promoting cancer progression, we find that elevated GFPT2 expression correlates with poor clinical outcome in NSCLC. Modulation of GFPT2 activity offers a potentially important therapeutic target to combat NSCLC disease progression.

Indexed as

A549 CellsCarcinoma, Non-Small-Cell LungCell MovementGene Expression Regulation, NeoplasticGlutamine-Fructose-6-Phosphate Transaminase (Isomerizing)HEK293 CellsHumansLung NeoplasmsNF-kappa BSignal TransductionSirtuinsTranscriptional ActivationGFPT2 protein, humanGlutamine-Fructose-6-Phosphate Transaminase (Isomerizing)NF-kappa BSIRT6 protein, humanSirtuinsCell migrationEpithelial-mesenchymal transitionGlutamine-fructose-6-phosphate transaminase 2 (GFPT2)Non-small cell lung cancer (NSCLC)Nuclear factor kappa B (NF-κB)Sirtuin-6 (SIRT6)

Identifiers

PMID30885209
PMCPMC6421657
OpenAlexW2940568281

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.