Evidence map›Paper›PMID 37383672›Full record

ArticlePrecision clinical medicine2023

Genetic factors for differentiated thyroid cancer in French Polynesia: new candidate loci.

Monia Zidane, Marc Haber, Thérèse Truong, Frédérique Rachédi, Catherine Ory, Sylvie Chevillard, Hélène Blanché, Robert Olaso, Anne Boland, Éric Conte and 11 more

Open access · diamondAbstract read
In one paragraph

Article in Precision clinical medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 1 citations in OpenAlex.

  1. Pooled it
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

21 authors at 8 institutions in 4 countries.

Monia ZidaneUniversity Paris-Saclay, UVSQ, Inserm, Gustave Roussy, CESP, Team "Radiations Epidemiology", Villejuif 94805, France.
Marc HaberCentre for Computational Biology, University of Birmingham, Birmingham B152TT, UK.
Thérèse TruongUniversity Paris-Saclay, UVSQ, Inserm, Gustave Roussy, CESP, Team "Exposome and Heredity", Villejuif 94805, France.
Frédérique RachédiEndocrinology Unit, Territorial Hospital Taaone, F-98713, Papeete, Tahiti 98713, French Polynesia.
Catherine OryCEA, Laboratoire de Cancérologie Fondamentale, Institut de Biologie François Jacob, iRCM, SREIT, Laboratoire de Cancérologie Expérimentale (LCE), Université Paris-Saclay, Fontenay aux Roses 92265, France.
Sylvie ChevillardCEA, Laboratoire de Cancérologie Fondamentale, Institut de Biologie François Jacob, iRCM, SREIT, Laboratoire de Cancérologie Expérimentale (LCE), Université Paris-Saclay, Fontenay aux Roses 92265, France.
Hélène BlanchéFondation Jean Dausset-Centre d'Etude du Polymorphisme Humain, Paris 75010, France.
Robert OlasoUniversité Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, Evry 91057, France.
Anne BolandUniversité Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, Evry 91057, France.
Éric ConteU.S.R. 2003 (CNRS / UPF), Faa'a, Tahiti 98702, France.
Mojgan KarimiUniversity Paris-Saclay, UVSQ, Inserm, Gustave Roussy, CESP, Team "Exposome and Heredity", Villejuif 94805, France.
Yan RenUniversity Paris-Saclay, UVSQ, Inserm, Gustave Roussy, CESP, Team "Radiations Epidemiology", Villejuif 94805, France.
Constance XhaardUniversity of Lorraine, INSERM CIC 1433, Nancy CHRU, INSERM U1116, Nancy 54500, France.
Vincent SouchardUniversity Paris-Saclay, UVSQ, Inserm, Gustave Roussy, CESP, Team "Radiations Epidemiology", Villejuif 94805, France.
Jacques GardonHydrosciences Montpellier, Research Institute for Development, CNRS, University of Montpellier, Montpellier 62307, France.
Marc TaquetResearch Institute for Development, Center IRD on Tahiti, Arue, Tahiti 98713, French Polynesia.
André BouvilleNational Cancer Institute (retired), Bethesda, MD 20892, USA.
Jean-François DeleuzeFondation Jean Dausset-Centre d'Etude du Polymorphisme Humain, Paris 75010, France.
Vladimir DrozdovitchDivision of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Bethesda, MD 20892, USA.
Florent de VathaireUniversity Paris-Saclay, UVSQ, Inserm, Gustave Roussy, CESP, Team "Radiations Epidemiology", Villejuif 94805, France.
Jean-Baptiste CazierCentre for Computational Biology, University of Birmingham, Birmingham B152TT, UK.
Inserm · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRCentre National de la Recherche Scientifique · FRUniversity of Birmingham · GBFondation Jean Dausset-CEPH · FRInstitut Louis Malardé · PFNational Cancer Institute · USUnited States Department of Health and Human Services · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Populations of French Polynesia (FP), where France performed atmospheric tests between 1966 and 1974, experience a high incidence of differentiated thyroid cancer (DTC). However, up to now, no sufficiently large study of DTC genetic factors in this population has been performed to reach definitive conclusion. This research aimed to analyze the genetic factors of DTC risk among the native FP populations. Methods: We analyzed more than 300 000 single nucleotide polymorphisms (SNPs) genotyped in 283 DTC cases and 418 matched controls born in FP, most being younger than 15 years old at the time of the first nuclear tests. We analyzed the genetic profile of our cohort to identify population subgroups. We then completed a genome-wide analysis study on the whole population. Results: We identified a specific genetic structure in the FP population reflecting admixture from Asian and European populations. We identified three regions associated with increased DTC risk at 6q24.3, 10p12.2, and 17q21.32. The lead SNPs at these loci showed respective p-values of 1.66 × 10 Conclusion: Our study results suggest a role of the loci 6q24.3, 10p12.2 and 17q21.32 in DTC risk. However, a whole genome sequencing approach would be better suited to characterize these factors than genotyping with microarray chip designed for the Caucasian population. Moreover, the functional impact of these three new loci needs to be further explored and validated.

Indexed as

differentiated thyroid cancergenetic susceptibilitypopulation genetics

Identifiers

PMID37383672
PMCPMC10294640
OpenAlexW4380442203

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.