Evidence map›Paper›PMID 32611766›Full record

ArticleThe Journal of biological chemistry2020

The transcription factors aryl hydrocarbon receptor and MYC cooperate in the regulation of cellular metabolism.

M Carmen Lafita-Navarro, Lizbeth Perez-Castro, Lauren G Zacharias, Spencer Barnes, Ralph J DeBerardinis, Maralice Conacci-Sorrell

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 37 citations in OpenAlex.

  1. MAIT cell plasticity generates CD4Cellular & molecular immunology · 2026
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  9. Regulatory mechanisms of one-carbon metabolism enzymes.The Journal of biological chemistry · 2023
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Nucleolar stress: From development to cancer.Seminars in cell & developmental biology · 2023
    Review
  15. Article
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  18. 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.

M Carmen Lafita-NavarroDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID 0000-0002-7266-651X
Lizbeth Perez-CastroDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Lauren G ZachariasChildren's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Spencer BarnesBioinformatics Core Facility, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Ralph J DeBerardinisChildren's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Maralice Conacci-SorrellDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas, USA Maralice.ConacciSorrell@UTSouthwestern.edu.
The University of Texas Southwestern Medical Center · USChildren's Medical Center · USSouthwestern Medical Center · US

Funding

The kynurenine-AHR pathway in biomass production - Revision - 2R01CA245548 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI CONACCI-SORRELL, MARALICE · 2020 to 2024
$2.2M
NCI NIH HHS R01 CA245548
6 · The paper itself

Abstract

The transcription factor AHR (aryl hydrocarbon receptor) drives the expression of genes involved in detoxification pathways in cells exposed to pollutants and other small molecules. Moreover, AHR supports transcriptional programs that promote ribosome biogenesis and protein synthesis in cells stimulated to proliferate by the oncoprotein MYC. Thus, AHR is necessary for the proliferation of MYC-overexpressing cells. To define metabolic pathways in which AHR cooperates with MYC in supporting cell growth, here we used LC-MS-based metabolomics to examine the metabolome of MYC-expressing cells upon

Indexed as

Metabolic Networks and PathwaysBasic Helix-Loop-Helix ProteinsCell Line, TumorDihydroorotate DehydrogenaseGene Expression Regulation, EnzymologicGene Knockdown TechniquesHumansL-Lactate DehydrogenaseMultienzyme ComplexesOrotate PhosphoribosyltransferaseOrotidine-5'-Phosphate DecarboxylaseOxidoreductases Acting on CH-CH Group DonorsProto-Oncogene Proteins c-mycReceptors, Aryl HydrocarbonAHR protein, humanBasic Helix-Loop-Helix ProteinsDihydroorotate DehydrogenaseLDHA protein, humanL-Lactate DehydrogenaseMultienzyme ComplexesMYC protein, humanOrotate PhosphoribosyltransferaseOrotidine-5'-Phosphate DecarboxylaseOxidoreductases Acting on CH-CH Group DonorsProto-Oncogene Proteins c-mycReceptors, Aryl Hydrocarbonuridine 5'-monophosphate synthasearyl hydrocarbon receptor (AHR)cancergene regulationglioblastomaglycolysismetabolismmetabolomicsMYC (c-Myc)oncogenepyrimidine

Identifiers

PMID32611766
PMCPMC7458811
OpenAlexW3040639806

What OpenQuestion holds

Textmetadata
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.