Evidence map›Paper›PMID 29696133›Full record

ArticleFrontiers in oncology2018

Classical NF-κB Metabolically Reprograms Sarcoma Cells Through Regulation of Hexokinase 2.

Priya Londhe, Peter Y Yu, Yuichi Ijiri, Katherine J Ladner, Joelle M Fenger, Cheryl London, Peter J Houghton, Denis C Guttridge

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.0field-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

45 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
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  10. NFκB and JNK pathways mediate metabolic adaptation upon ESCRT-I deficiency.Cellular and molecular life sciences : CMLS · 2024
    Article
  11. Article
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  15. Functional Profiling of Soft Tissue Sarcoma Using Mechanistic Models.International journal of molecular sciences · 2023
    Article
  16. Article
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  18. Review
  19. Article
  20. On the Relevance of Soft Tissue Sarcomas Metabolic Landscape Mapping.International journal of molecular sciences · 2022
    Review
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.

Priya LondheDepartment of Cancer Biology and Genetics, The Ohio State University, Columbus, OH, United States.
Peter Y YuArthur G. James Comprehensive Cancer Center, The Ohio State University, Columbus, OH, United States.
Yuichi IjiriDepartment of Cancer Biology and Genetics, The Ohio State University, Columbus, OH, United States.
Katherine J LadnerDepartment of Cancer Biology and Genetics, The Ohio State University, Columbus, OH, United States.
Joelle M FengerDepartment of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH, United States.
Cheryl LondonDepartment of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH, United States.
Peter J HoughtonGreehey Children's Research Institute, University of Texas Health Science Center, San Antonio, TX, United States.
Denis C GuttridgeDepartment of Cancer Biology and Genetics, The Ohio State University, Columbus, OH, United States.
The Ohio State University · USThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · USThe University of Texas Health Science Center at San Antonio · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
The Ohio State University Center for clinical and Translational ScienceUL1TR001070 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2013 to 2017
$22.6M
Elucidating the role of NF-kB signaling in rhabdomyocarcomaR01CA143082 · NCI · OHIO STATE UNIVERSITY · PI GUTTRIDGE, DENIS C, KELLER, CHARLES · 2011 to 2015
$1.6M
Dissecting the role of miR-9 in normal and malignant mast cell biologyK01OD019923 · OD · OHIO STATE UNIVERSITY · PI FENGER, JOELLE M · 2015 to 2019
$654k
NCATS NIH HHS UL1 TR001070NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA143082NIH HHS K01 OD019923
6 · The paper itself

Abstract

backgroundMetabolic reprogramming has emerged as a cancer hallmark, and one of the well-known cancer-associated metabolic alterations is the increase in the rate of glycolysis. Recent reports have shown that both the classical and alternative signaling pathways of nuclear factor κB (NF-κB) play important roles in controlling the metabolic profiles of normal cells and cancer cells. However, how these signaling pathways affect the metabolism of sarcomas, specifically rhabdomyosarcoma (RMS) and osteosarcoma (OS), has not been characterized.

methodsClassical NF-κB activity was inhibited through overexpression of the IκBα super repressor of NF-κB in RMS and OS cells. Global gene expression analysis was performed using Affymetrix GeneChip Human Transcriptome Array 2.0, and data were interpreted using gene set enrichment analysis. Seahorse Bioscience XF

resultsInhibition of classical NF-κB activity in sarcoma cell lines restored alternative signaling as well as an increased oxidative respiratory metabolic phenotype

conclusionThese findings suggest that classical signaling of NF-κB plays a crucial role in the metabolic profile of pediatric sarcomas potentially through the regulation of HK2.

Indexed as

hexokinasemetabolismnuclear factor kappa Bosteosarcomarhabdomyosarcomasarcoma

Identifiers

PMID29696133
PMCPMC5904193
OpenAlexW2797119600

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.