Evidence map›Paper›PMID 30254109›Full record

ArticleGenes & development2018

The aryl hydrocarbon receptor regulates nucleolar activity and protein synthesis in MYC-expressing cells.

M Carmen Lafita-Navarro, Min Kim, Nofit Borenstein-Auerbach, Niranjan Venkateswaran, Yi-Heng Hao, Roshni Ray, Thomas Brabletz, Pier Paolo Scaglioni, Jerry W Shay, Maralice Conacci-Sorrell

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2018. 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
–field-weighted citation impact
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, 43 citations in OpenAlex.

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  16. Roles of NOLC1 in cancers and viral infection.Journal of cancer research and clinical oncology · 2023
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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

10 authors at 3 institutions in 2 countries.

M Carmen Lafita-NavarroDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Min KimLyda Hill Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Nofit Borenstein-AuerbachDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Niranjan VenkateswaranDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Yi-Heng HaoDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Roshni RayDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Thomas BrabletzNikolaus-Fiebiger-Center for Molecular Medicine, University Erlangen-Nurnberg, 91054 Erlangen, Germany.
Pier Paolo ScaglioniDepartment of Medicine, Division of Hematology Oncology, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267, USA.
Jerry W ShayDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Maralice Conacci-SorrellDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
The University of Texas Southwestern Medical Center · USFriedrich-Alexander-Universität Erlangen-Nürnberg · DEUniversity of Cincinnati Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MYC enhances protein synthesis by regulating genes involved in ribosome biogenesis and protein translation. Here, we show that MYC-induced protein translation is mediated by the transcription factor aryl hydrocarbon receptor (AHR), which is induced by MYC in colonic cells. AHR promotes protein synthesis by activating the transcription of genes required for ribosome biogenesis and protein translation, including OGFOD1 and NOLC1. Using surface sensing of translation (SUnSET) to measure global protein translation, we found that silencing AHR or its targets diminishes protein synthesis. Therefore, targeting AHR or its downstream pathways could provide a novel approach to limit biomass production in MYC-driven tumors.

Indexed as

Protein BiosynthesisAnimalsCell LineCell NucleolusCells, CulturedColonic NeoplasmsHumansProto-Oncogene Proteins c-mycRatsReceptors, Aryl HydrocarbonTranscriptional ActivationProto-Oncogene Proteins c-mycReceptors, Aryl HydrocarbonAHRaryl hydrocarbon receptorcancerMycnucleolusribosome biogenesistranscriptiontranslation

Identifiers

PMID30254109
PMCPMC6169836
OpenAlexW2893917847

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.