Circadian genes polymorphisms, night work and prostate cancer risk: Findings from the EPICAP study.


Journal

International journal of cancer
ISSN: 1097-0215
Titre abrégé: Int J Cancer
Pays: United States
ID NLM: 0042124

Informations de publication

Date de publication:
01 12 2020
Historique:
received: 30 09 2019
revised: 04 05 2020
accepted: 18 05 2020
pubmed: 9 6 2020
medline: 17 4 2021
entrez: 8 6 2020
Statut: ppublish

Résumé

Over the past two decades, several studies have attempted to understand the hypothesis that disrupting the circadian rhythm may promote the development of cancer. Some have suggested that night work and some circadian genes polymorphisms are associated with cancer, including prostate cancer. Our study aims to test the hypothesis that prostate cancer risk among night workers may be modulated by genetic polymorphisms in the circadian pathway genes based on data from the EPICAP study, a population-based case-control study including 1511 men (732 cases/779 controls) with genotyped data. We estimated odds ratio (ORs) and P values of the association between prostate cancer and circadian gene variants using logistic regression models. We tested the interaction between circadian genes variants and night work indicators that were significantly associated with prostate cancer at pathway, gene and SNP levels. Analyses were also stratified by each of these night work indicators and by cancer aggressiveness. The circadian pathway was significantly associated with aggressive prostate cancer among night workers (P = .004), particularly for men who worked at night for <20 years (P = .0002) and those who performed long night shift (>10 hours, P = .001). At the gene level, we observed among night workers significant associations between aggressive prostate cancer and ARNTL, NPAS2 and RORA. At the SNP-level, no significant association was observed. Our findings provide some clues of a potential modulating effect of circadian genes in the relationship between night work and prostate cancer. Further investigation is warranted to confirm these findings and to better elucidate the biological pathways involved.

Identifiants

pubmed: 32506468
doi: 10.1002/ijc.33139
doi:

Substances chimiques

ARNTL Transcription Factors 0
BMAL1 protein, human 0
Basic Helix-Loop-Helix Transcription Factors 0
NPAS2 protein, human 0
Nerve Tissue Proteins 0
Nuclear Receptor Subfamily 1, Group F, Member 1 0
RORA protein, human 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3119-3129

Informations de copyright

© 2020 UICC.

Références

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Auteurs

Méyomo G Wendeu-Foyet (MG)

Université Paris-Saclay, UVSQ, Inserm, CESP, Villejuif, France.

Sylvie Cénée (S)

Université Paris-Saclay, UVSQ, Inserm, CESP, Villejuif, France.

Yves Koudou (Y)

Université Paris-Saclay, UVSQ, Inserm, CESP, Villejuif, France.

Brigitte Trétarre (B)

Registre des Tumeurs de l'Hérault, EA 2415, ICM, Montpellier, France.

Xavier Rébillard (X)

Clinique Beau Soleil, Service Urologie, Montpellier, France.

Géraldine Cancel-Tassin (G)

CeRePP, Hopital Tenon, Paris, France.
Sorbonne Université, GRC no. 5, ONCOTYPE-URO, AP-HP, Hôpital Tenon, Paris, France.

Olivier Cussenot (O)

CeRePP, Hopital Tenon, Paris, France.
Sorbonne Université, GRC no. 5, ONCOTYPE-URO, AP-HP, Hôpital Tenon, Paris, France.

Anne Boland (A)

Centre National de Recherche en Génomique Humaine (CNRGH), Institut de Biologie François Jacob, CEA, Université Paris-Saclay, Saint-Aubin, France.

Robert Olaso (R)

Centre National de Recherche en Génomique Humaine (CNRGH), Institut de Biologie François Jacob, CEA, Université Paris-Saclay, Saint-Aubin, France.

Jean-François Deleuze (JF)

Centre National de Recherche en Génomique Humaine (CNRGH), Institut de Biologie François Jacob, CEA, Université Paris-Saclay, Saint-Aubin, France.

Hélène Blanché (H)

Centre d'Etude du Polymorphisme Humain (CEPH), Fondation Jean Dausset, Paris, France.

Pierre-Jean Lamy (PJ)

Clinique Beau Soleil, Service Urologie, Montpellier, France.
Institut médical d'Analyse Génomique-Imagenome, Labosud, Montpellier, France.

Claire Mulot (C)

Université Paris Descartes, INSERM UMR-S1147 EPIGENETEC, Paris, France.

Pierre Laurent-Puig (P)

Université Paris Descartes, INSERM UMR-S1147 EPIGENETEC, Paris, France.

Thérèse Truong (T)

Université Paris-Saclay, UVSQ, Inserm, CESP, Villejuif, France.

Florence Menegaux (F)

Université Paris-Saclay, UVSQ, Inserm, CESP, Villejuif, France.

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