Evidence map›Paper›PMID 33903625›Full record

Trial reportScientific reports2021

Gene network and biological pathways associated with susceptibility to differentiated thyroid carcinoma.

Om Kulkarni, Pierre-Emmanuel Sugier, Julie Guibon, Anne Boland-Augé, Christine Lonjou, Delphine Bacq-Daian, Robert Olaso, Carole Rubino, Vincent Souchard, Frédérique Rachedi and 15 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Arsenite toxicity is regulated by queuine availability and oxidation-induced reprogramming of the human tRNA epitranscriptome.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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

25 authors at 12 institutions in 3 countries.

Om KulkarniInserm, U900, Institut Curie, PSL University, Mines ParisTech, 75248, Paris, France.
Pierre-Emmanuel SugierUniversité Paris-Saclay, UVSQ, Gustave Roussy, Inserm, CESP, 94807, Villejuif, France.
Julie GuibonInserm, U900, Institut Curie, PSL University, Mines ParisTech, 75248, Paris, France.
Anne Boland-AugéUniversité Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, 91057, Evry, France.
Christine LonjouInserm, U900, Institut Curie, PSL University, Mines ParisTech, 75248, Paris, France.
Delphine Bacq-DaianUniversité Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, 91057, Evry, France.
Robert OlasoUniversité Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, 91057, Evry, France.
Carole RubinoUniversité Paris-Saclay, UVSQ, Gustave Roussy, Inserm, CESP, 94807, Villejuif, France.
Vincent SouchardUniversité Paris-Saclay, UVSQ, Gustave Roussy, Inserm, CESP, 94807, Villejuif, France.
Frédérique RachediCentre Hospitalier Territorial de Polynésie Française, CHTPF, Pirae, Tahiti, 98713, Papeete, French Polynesia.
Juan Jesus Lence-AntaInstituto Nacional de Oncologia y de Radiobiologia, INOR, La Havana, Cuba.
Rosa Maria OrtizInstituto Nacional de Oncologia y de Radiobiologia, INOR, La Havana, Cuba.
Constance XhaardUniversité Paris-Saclay, UVSQ, Gustave Roussy, Inserm, CESP, 94807, Villejuif, France.
Pierre Laurent-PuigCentre de Recherche des Cordeliers, INSERM, Sorbonne Université, USPC, Université Paris Descartes, Université Paris Diderot, EPIGENETEC, 75006, Paris, France.
Claire MulotCentre de Recherche des Cordeliers, INSERM, Sorbonne Université, USPC, Université Paris Descartes, Université Paris Diderot, EPIGENETEC, 75006, Paris, France.
Anne-Valérie GuizardRegistre Général des Tumeurs du Calvados, Centre François Baclesse, 14000, Caen, France.
Claire SchvartzRegistre des Cancers Thyroïdiens, Institut Jean Godinot, 51100, Reims, France.
Marie-Christine Boutron-RuaultUniversité Paris-Saclay, UVSQ, Gustave Roussy, Inserm, CESP, 94807, Villejuif, France.
Evgenia OstroumovaEnvironment and Radiation Section, International Agency for Research on Cancer, 69008, Lyon, France.
Ausrele KesminieneEnvironment and Radiation Section, International Agency for Research on Cancer, 69008, Lyon, France.
Jean-François DeleuzeUniversité Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, 91057, Evry, France.
Pascal GuénelUniversité Paris-Saclay, UVSQ, Gustave Roussy, Inserm, CESP, 94807, Villejuif, France.
Florent De VathaireUniversité Paris-Saclay, UVSQ, Gustave Roussy, Inserm, CESP, 94807, Villejuif, France.
Thérèse Truong *Université Paris-Saclay, UVSQ, Gustave Roussy, Inserm, CESP, 94807, Villejuif, France.
Fabienne Lesueur *Inserm, U900, Institut Curie, PSL University, Mines ParisTech, 75248, Paris, France. fabienne.lesueur@curie.fr.
Inserm · FRCancer et génome: Bioinformatique, biostatistiques et épidémiologie des systèmes complexesInstitut Gustave Roussy · FRUniversité Paris-Saclay · FRCEA Paris-Saclay · FRCentre International de Recherche sur le Cancer · FRDélégation Paris 7 · FRInstituto de Oncología y Radiobiología · CUCentre François Baclesse · FRInstitut Jean Godinot · FRUniversité de Versailles Saint-Quentin-en-Yvelines · FRUniversity of French Polynesia · PF

Funding

World Health Organization 001
6 · The paper itself

Abstract

Variants identified in earlier genome-wide association studies (GWAS) on differentiated thyroid carcinoma (DTC) explain about 10% of the overall estimated genetic contribution and could not provide complete insights into biological mechanisms involved in DTC susceptibility. Integrating systems biology information from model organisms, genome-wide expression data from tumor and matched normal tissue and GWAS data could help identifying DTC-associated genes, and pathways or functional networks in which they are involved. We performed data mining of GWAS data of the EPITHYR consortium (1551 cases and 1957 controls) using various pathways and protein-protein interaction (PPI) annotation databases and gene expression data from The Cancer Genome Atlas. We identified eight DTC-associated genes at known loci 2q35 (DIRC3), 8p12 (NRG1), 9q22 (FOXE1, TRMO, HEMGN, ANP32B, NANS) and 14q13 (MBIP). Using the EW_dmGWAS approach we found that gene networks related to glycogenolysis, glycogen metabolism, insulin metabolism and signal transduction pathways associated with muscle contraction were overrepresented with association signals (false discovery rate adjusted p-value < 0.05). Additionally, suggestive association of 21 KEGG and 75 REACTOME pathways with DTC indicate a link between DTC susceptibility and functions related to metabolism of cholesterol, amino sugar and nucleotide sugar metabolism, steroid biosynthesis, and downregulation of ERBB2 signaling pathways. Together, our results provide novel insights into biological mechanisms contributing to DTC risk.

Indexed as

Gene Regulatory NetworksGenetic Predisposition to DiseaseGenotypePolymorphism, Single NucleotideAdolescentAdultChildChild, PreschoolFemaleGenome-Wide Association StudyHumansInfantInfant, NewbornMaleMiddle AgedNeoplasm ProteinsNeoplasm Proteins

Identifiers

PMID33903625
PMCPMC8076215
OpenAlexW3157690797

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.