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Inherited variation in circadian rhythm genes and risks of prostate cancer and three other cancer sites in combined cancer consortia.

Identifieur interne : 000979 ( Main/Exploration ); précédent : 000978; suivant : 000980

Inherited variation in circadian rhythm genes and risks of prostate cancer and three other cancer sites in combined cancer consortia.

Auteurs : Fangyi Gu [États-Unis] ; Han Zhang [États-Unis] ; Paula L. Hyland [États-Unis] ; Sonja Berndt [États-Unis] ; Susan M. Gapstur [États-Unis] ; William Wheeler [États-Unis] ; The Ellipse Consortium ; Christopher I. Amos [États-Unis] ; Stephane Bezieau [France] ; Heike Bickeböller [Allemagne] ; Hermann Brenner [Allemagne] ; Paul Brennan [France] ; Jenny Chang-Claude [Allemagne] ; David V. Conti [États-Unis] ; Jennifer Anne Doherty [États-Unis] ; Stephen B. Gruber [États-Unis] ; Tabitha A. Harrison [États-Unis] ; Richard B. Hayes [États-Unis] ; Michael Hoffmeister [Allemagne] ; Richard S. Houlston [Royaume-Uni] ; Rayjean J. Hung [Canada] ; Mark A. Jenkins [Australie] ; Peter Kraft [États-Unis] ; Kate Lawrenson [États-Unis] ; James Mckay [France] ; Sarah Markt [États-Unis] ; Lorelei Mucci [États-Unis] ; Catherine M. Phelan [États-Unis] ; Conghui Qu [États-Unis] ; Angela Risch [Autriche] ; Mary Anne Rossing [États-Unis] ; H-Erich Wichmann [Allemagne] ; Jianxin Shi [États-Unis] ; Eva Schernhammer [États-Unis] ; Kai Yu [États-Unis] ; Maria Teresa Landi [États-Unis] ; Neil E. Caporaso [États-Unis]

Source :

RBID : pubmed:28699174

Descripteurs français

English descriptors

Abstract

Circadian disruption has been linked to carcinogenesis in animal models, but the evidence in humans is inconclusive. Genetic variation in circadian rhythm genes provides a tool to investigate such associations. We examined associations of genetic variation in nine core circadian rhythm genes and six melatonin pathway genes with risk of colorectal, lung, ovarian and prostate cancers using data from the Genetic Associations and Mechanisms in Oncology (GAME-ON) network. The major results for prostate cancer were replicated in the Prostate, Lung, Colorectal and Ovarian (PLCO) cancer screening trial, and for colorectal cancer in the Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO). The total number of cancer cases and controls was 15,838/18,159 for colorectal, 14,818/14,227 for prostate, 12,537/17,285 for lung and 4,369/9,123 for ovary. For each cancer site, we conducted gene-based and pathway-based analyses by applying the summary-based Adaptive Rank Truncated Product method (sARTP) on the summary association statistics for each SNP within the candidate gene regions. Aggregate genetic variation in circadian rhythm and melatonin pathways were significantly associated with the risk of prostate cancer in data combining GAME-ON and PLCO, after Bonferroni correction (ppathway  < 0.00625). The two most significant genes were NPAS2 (pgene  = 0.0062) and AANAT (pgene  = 0.00078); the latter being significant after Bonferroni correction. For colorectal cancer, we observed a suggestive association with the circadian rhythm pathway in GAME-ON (ppathway  = 0.021); this association was not confirmed in GECCO (ppathway  = 0.76) or the combined data (ppathway  = 0.17). No significant association was observed for ovarian and lung cancer. These findings support a potential role for circadian rhythm and melatonin pathways in prostate carcinogenesis. Further functional studies are needed to better understand the underlying biologic mechanisms.

DOI: 10.1002/ijc.30883
PubMed: 28699174


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<name sortKey="Jenkins, Mark A" sort="Jenkins, Mark A" uniqKey="Jenkins M" first="Mark A" last="Jenkins">Mark A. Jenkins</name>
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<name sortKey="Kraft, Peter" sort="Kraft, Peter" uniqKey="Kraft P" first="Peter" last="Kraft">Peter Kraft</name>
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<country xml:lang="fr">États-Unis</country>
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<region type="state">Massachusetts</region>
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<name sortKey="Lawrenson, Kate" sort="Lawrenson, Kate" uniqKey="Lawrenson K" first="Kate" last="Lawrenson">Kate Lawrenson</name>
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<name sortKey="Markt, Sarah" sort="Markt, Sarah" uniqKey="Markt S" first="Sarah" last="Markt">Sarah Markt</name>
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<nlm:affiliation>Department of Epidemiology, Harvard T.H Chan School of Public Health, Boston, MA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<placeName>
<region type="state">Massachusetts</region>
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<wicri:cityArea>Department of Epidemiology, Harvard T.H Chan School of Public Health, Boston</wicri:cityArea>
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<name sortKey="Mucci, Lorelei" sort="Mucci, Lorelei" uniqKey="Mucci L" first="Lorelei" last="Mucci">Lorelei Mucci</name>
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<nlm:affiliation>Department of Epidemiology, Harvard T.H Chan School of Public Health, Boston, MA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
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<region type="state">Massachusetts</region>
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<name sortKey="Phelan, Catherine M" sort="Phelan, Catherine M" uniqKey="Phelan C" first="Catherine M" last="Phelan">Catherine M. Phelan</name>
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<nlm:affiliation>Department of Cancer Epidemiology, Population Sciences Division, Moffitt Cancer Center, Tampa, FL.</nlm:affiliation>
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<region type="state">Floride</region>
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<wicri:cityArea>Department of Cancer Epidemiology, Population Sciences Division, Moffitt Cancer Center, Tampa</wicri:cityArea>
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<name sortKey="Qu, Conghui" sort="Qu, Conghui" uniqKey="Qu C" first="Conghui" last="Qu">Conghui Qu</name>
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<name sortKey="Risch, Angela" sort="Risch, Angela" uniqKey="Risch A" first="Angela" last="Risch">Angela Risch</name>
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<name sortKey="Rossing, Mary Anne" sort="Rossing, Mary Anne" uniqKey="Rossing M" first="Mary Anne" last="Rossing">Mary Anne Rossing</name>
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<nlm:affiliation>Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA.</nlm:affiliation>
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<name sortKey="Shi, Jianxin" sort="Shi, Jianxin" uniqKey="Shi J" first="Jianxin" last="Shi">Jianxin Shi</name>
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<nlm:affiliation>Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD.</nlm:affiliation>
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<region type="state">Maryland</region>
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<name sortKey="Schernhammer, Eva" sort="Schernhammer, Eva" uniqKey="Schernhammer E" first="Eva" last="Schernhammer">Eva Schernhammer</name>
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<nlm:affiliation>Department of Epidemiology, Harvard T.H Chan School of Public Health, Boston, MA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<placeName>
<region type="state">Massachusetts</region>
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<wicri:cityArea>Department of Epidemiology, Harvard T.H Chan School of Public Health, Boston</wicri:cityArea>
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<name sortKey="Yu, Kai" sort="Yu, Kai" uniqKey="Yu K" first="Kai" last="Yu">Kai Yu</name>
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<nlm:affiliation>Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<placeName>
<region type="state">Maryland</region>
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<wicri:cityArea>Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville</wicri:cityArea>
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<name sortKey="Landi, Maria Teresa" sort="Landi, Maria Teresa" uniqKey="Landi M" first="Maria Teresa" last="Landi">Maria Teresa Landi</name>
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<nlm:affiliation>Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<placeName>
<region type="state">Maryland</region>
</placeName>
<wicri:cityArea>Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville</wicri:cityArea>
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<name sortKey="Caporaso, Neil E" sort="Caporaso, Neil E" uniqKey="Caporaso N" first="Neil E" last="Caporaso">Neil E. Caporaso</name>
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<region type="state">Massachusetts</region>
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<region type="state">Floride</region>
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<region type="state">Maryland</region>
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<region type="state">Massachusetts</region>
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<term>Arylalkylamine N-Acetyltransferase (génétique)</term>
<term>Carcinogenèse (génétique)</term>
<term>Facteurs de transcription à motif basique hélice-boucle-hélice (génétique)</term>
<term>Femelle</term>
<term>Humains</term>
<term>Mâle</term>
<term>Polymorphisme de nucléotide simple</term>
<term>Protéines de tissu nerveux (génétique)</term>
<term>Prédisposition génétique à une maladie</term>
<term>Rythme circadien (génétique)</term>
<term>Transduction du signal (génétique)</term>
<term>Tumeurs colorectales (anatomopathologie)</term>
<term>Tumeurs colorectales (génétique)</term>
<term>Tumeurs de l'ovaire (anatomopathologie)</term>
<term>Tumeurs de l'ovaire (génétique)</term>
<term>Tumeurs de la prostate (anatomopathologie)</term>
<term>Tumeurs de la prostate (génétique)</term>
<term>Tumeurs du poumon (anatomopathologie)</term>
<term>Tumeurs du poumon (génétique)</term>
<term>Études d'associations génétiques</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Arylalkylamine N-Acetyltransferase</term>
<term>Basic Helix-Loop-Helix Transcription Factors</term>
<term>Nerve Tissue Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr">
<term>Tumeurs colorectales</term>
<term>Tumeurs de l'ovaire</term>
<term>Tumeurs de la prostate</term>
<term>Tumeurs du poumon</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Carcinogenesis</term>
<term>Circadian Rhythm</term>
<term>Colorectal Neoplasms</term>
<term>Lung Neoplasms</term>
<term>Ovarian Neoplasms</term>
<term>Prostatic Neoplasms</term>
<term>Signal Transduction</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Arylalkylamine N-Acetyltransferase</term>
<term>Carcinogenèse</term>
<term>Facteurs de transcription à motif basique hélice-boucle-hélice</term>
<term>Protéines de tissu nerveux</term>
<term>Rythme circadien</term>
<term>Transduction du signal</term>
<term>Tumeurs colorectales</term>
<term>Tumeurs de l'ovaire</term>
<term>Tumeurs de la prostate</term>
<term>Tumeurs du poumon</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Colorectal Neoplasms</term>
<term>Lung Neoplasms</term>
<term>Ovarian Neoplasms</term>
<term>Prostatic Neoplasms</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Female</term>
<term>Genetic Association Studies</term>
<term>Genetic Predisposition to Disease</term>
<term>Humans</term>
<term>Male</term>
<term>Polymorphism, Single Nucleotide</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Femelle</term>
<term>Humains</term>
<term>Mâle</term>
<term>Polymorphisme de nucléotide simple</term>
<term>Prédisposition génétique à une maladie</term>
<term>Études d'associations génétiques</term>
</keywords>
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<front>
<div type="abstract" xml:lang="en">Circadian disruption has been linked to carcinogenesis in animal models, but the evidence in humans is inconclusive. Genetic variation in circadian rhythm genes provides a tool to investigate such associations. We examined associations of genetic variation in nine core circadian rhythm genes and six melatonin pathway genes with risk of colorectal, lung, ovarian and prostate cancers using data from the Genetic Associations and Mechanisms in Oncology (GAME-ON) network. The major results for prostate cancer were replicated in the Prostate, Lung, Colorectal and Ovarian (PLCO) cancer screening trial, and for colorectal cancer in the Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO). The total number of cancer cases and controls was 15,838/18,159 for colorectal, 14,818/14,227 for prostate, 12,537/17,285 for lung and 4,369/9,123 for ovary. For each cancer site, we conducted gene-based and pathway-based analyses by applying the summary-based Adaptive Rank Truncated Product method (sARTP) on the summary association statistics for each SNP within the candidate gene regions. Aggregate genetic variation in circadian rhythm and melatonin pathways were significantly associated with the risk of prostate cancer in data combining GAME-ON and PLCO, after Bonferroni correction (ppathway  < 0.00625). The two most significant genes were NPAS2 (pgene  = 0.0062) and AANAT (pgene  = 0.00078); the latter being significant after Bonferroni correction. For colorectal cancer, we observed a suggestive association with the circadian rhythm pathway in GAME-ON (ppathway  = 0.021); this association was not confirmed in GECCO (ppathway  = 0.76) or the combined data (ppathway  = 0.17). No significant association was observed for ovarian and lung cancer. These findings support a potential role for circadian rhythm and melatonin pathways in prostate carcinogenesis. Further functional studies are needed to better understand the underlying biologic mechanisms.</div>
</front>
</TEI>
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<li>Allemagne</li>
<li>Australie</li>
<li>Autriche</li>
<li>Canada</li>
<li>France</li>
<li>Royaume-Uni</li>
<li>États-Unis</li>
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<li>Bade-Wurtemberg</li>
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<li>District de Haute-Bavière</li>
<li>District de Karlsruhe</li>
<li>Floride</li>
<li>Géorgie (États-Unis)</li>
<li>Maryland</li>
<li>Massachusetts</li>
<li>New Hampshire</li>
<li>Pays de la Loire</li>
<li>Rhône-Alpes</li>
<li>Utah</li>
<li>Victoria (État)</li>
<li>Washington (État)</li>
<li>État de New York</li>
</region>
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<li>Göttingen</li>
<li>Heidelberg</li>
<li>Lyon</li>
<li>Melbourne</li>
<li>Munich</li>
<li>Nantes</li>
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<li>Université Louis-et-Maximilien de Munich</li>
<li>Université de Melbourne</li>
</orgName>
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<name sortKey="Hayes, Richard B" sort="Hayes, Richard B" uniqKey="Hayes R" first="Richard B" last="Hayes">Richard B. Hayes</name>
<name sortKey="Hyland, Paula L" sort="Hyland, Paula L" uniqKey="Hyland P" first="Paula L" last="Hyland">Paula L. Hyland</name>
<name sortKey="Kraft, Peter" sort="Kraft, Peter" uniqKey="Kraft P" first="Peter" last="Kraft">Peter Kraft</name>
<name sortKey="Landi, Maria Teresa" sort="Landi, Maria Teresa" uniqKey="Landi M" first="Maria Teresa" last="Landi">Maria Teresa Landi</name>
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<name sortKey="Qu, Conghui" sort="Qu, Conghui" uniqKey="Qu C" first="Conghui" last="Qu">Conghui Qu</name>
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<name sortKey="Zhang, Han" sort="Zhang, Han" uniqKey="Zhang H" first="Han" last="Zhang">Han Zhang</name>
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<name sortKey="Bezieau, Stephane" sort="Bezieau, Stephane" uniqKey="Bezieau S" first="Stephane" last="Bezieau">Stephane Bezieau</name>
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<name sortKey="Mckay, James" sort="Mckay, James" uniqKey="Mckay J" first="James" last="Mckay">James Mckay</name>
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<name sortKey="Bickeboller, Heike" sort="Bickeboller, Heike" uniqKey="Bickeboller H" first="Heike" last="Bickeböller">Heike Bickeböller</name>
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<name sortKey="Wichmann, H Erich" sort="Wichmann, H Erich" uniqKey="Wichmann H" first="H-Erich" last="Wichmann">H-Erich Wichmann</name>
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