Evidence map›Paper›PMID 35013311›Full record

ArticleNature communications2022

Alteration of ribosome function upon 5-fluorouracil treatment favors cancer cell drug-tolerance.

Gabriel Therizols, Zeina Bash-Imam, Baptiste Panthu, Christelle Machon, Anne Vincent, Julie Ripoll, Sophie Nait-Slimane, Mounira Chalabi-Dchar, Angéline Gaucherot, Maxime Garcia and 22 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. 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
4.2field-weighted citation impact, top 4% 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, 54 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

32 authors at 3 institutions in 1 country.

Gabriel TherizolsInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.
Zeina Bash-ImamInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.
Baptiste PanthuCIRI-Inserm U1111, Ecole Normale Supérieure de Lyon, Lyon, F-693643, France.ORCID http://orcid.org/0000-0001-9430-4061
Christelle MachonInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.ORCID http://orcid.org/0000-0002-4494-8034
Anne VincentInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.ORCID http://orcid.org/0000-0003-4616-7685
Julie RipollLIRMM, UMR 5506, University of Montpellier, CNRS, Montpellier, France.
Sophie Nait-SlimaneInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.
Mounira Chalabi-DcharInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.ORCID http://orcid.org/0000-0002-4539-589X
Angéline GaucherotInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.
Maxime GarciaInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.
Florian LaforêtsInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.ORCID http://orcid.org/0000-0002-0924-5691
Virginie MarcelInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.ORCID http://orcid.org/0000-0002-9557-8221
Jihane Boubaker-VitreIGF, Univ. Montpellier, CNRS, INSERM, Montpellier, France.
Marie-Ambre MonetInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.
Céline BouclierIGF, Univ. Montpellier, CNRS, INSERM, Montpellier, France.
Christophe VanbelleInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.
Guillaume SouahliaInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.
Elise BerthelInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.
Marie Alexandra AlbaretInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.ORCID http://orcid.org/0000-0003-3374-5298
Hichem C MertaniInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.ORCID http://orcid.org/0000-0002-5958-6662
Michel PrudhommeDepartment of Digestive Surgery, CHU Nimes, Univ Montpellier, Nimes, France.
Martin BertrandDepartment of Digestive Surgery, CHU Nimes, Univ Montpellier, Nimes, France.
Alexandre DavidIGF, Univ. Montpellier, CNRS, INSERM, Montpellier, France.ORCID http://orcid.org/0000-0003-3365-1339
Jean-Christophe SaurinInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.
Philippe BouvetInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.ORCID http://orcid.org/0000-0003-4524-2233
Eric RivalsLIRMM, UMR 5506, University of Montpellier, CNRS, Montpellier, France.ORCID http://orcid.org/0000-0003-3791-3973
Théophile OhlmannCIRI-Inserm U1111, Ecole Normale Supérieure de Lyon, Lyon, F-693643, France.
Jérôme GuittonInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.ORCID http://orcid.org/0000-0001-6180-5708
Nicole Dalla VeneziaInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France.ORCID http://orcid.org/0000-0002-4553-3535
Julie PannequinIGF, Univ. Montpellier, CNRS, INSERM, Montpellier, France.
Frédéric CatezInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France. frederic.catez@lyon.unicancer.fr.ORCID http://orcid.org/0000-0001-8255-9091
Jean-Jacques DiazInserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000, Lyon, France. jean-jacques.diaz@lyon.unicancer.fr.ORCID http://orcid.org/0000-0002-7914-4319
Université Claude Bernard Lyon 1 · FRCentre National de la Recherche Scientifique · FRUniversité de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mechanisms of drug-tolerance remain poorly understood and have been linked to genomic but also to non-genomic processes. 5-fluorouracil (5-FU), the most widely used chemotherapy in oncology is associated with resistance. While prescribed as an inhibitor of DNA replication, 5-FU alters all RNA pathways. Here, we show that 5-FU treatment leads to the production of fluorinated ribosomes exhibiting altered translational activities. 5-FU is incorporated into ribosomal RNAs of mature ribosomes in cancer cell lines, colorectal xenografts, and human tumors. Fluorinated ribosomes appear to be functional, yet, they display a selective translational activity towards mRNAs depending on the nature of their 5'-untranslated region. As a result, we find that sustained translation of IGF-1R mRNA, which encodes one of the most potent cell survival effectors, promotes the survival of 5-FU-treated colorectal cancer cells. Altogether, our results demonstrate that "man-made" fluorinated ribosomes favor the drug-tolerant cellular phenotype by promoting translation of survival genes.

Indexed as

Antimetabolites, AntineoplasticCell Line, TumorCell SurvivalColorectal NeoplasmsDNA, NeoplasmDNA ReplicationDrug Resistance, NeoplasmDrug ToleranceFluorouracilHalogenationHCT116 CellsHumansProtein BiosynthesisReceptor, IGF Type 1RibosomesRNA, MessengerAntimetabolites, AntineoplasticDNA, NeoplasmFluorouracilReceptor, IGF Type 1RNA, MessengerRNA, Ribosomal

Identifiers

PMID35013311
PMCPMC8748862
OpenAlexW4205930233

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.