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Genome-Wide Measures of Peripheral Blood Dna Methylation and Prostate Cancer Risk in a Prospective Nested Case-Control Study.

Identifieur interne : 000D94 ( PubMed/Corpus ); précédent : 000D93; suivant : 000D95

Genome-Wide Measures of Peripheral Blood Dna Methylation and Prostate Cancer Risk in a Prospective Nested Case-Control Study.

Auteurs : Liesel M. Fitzgerald ; Haroon Naeem ; Enes Makalic ; Daniel F. Schmidt ; James G. Dowty ; Jihoon E. Joo ; Chol-Hee Jung ; Julie K. Bassett ; Pierre-Antoine Dugue ; Jessica Chung ; Andrew Lonie ; Roger L. Milne ; Ee Ming Wong ; John L. Hopper ; Dallas R. English ; Gianluca Severi ; Laura Baglietto ; John Pedersen ; Graham G. Giles ; Melissa C. Southey

Source :

RBID : pubmed:28116812

English descriptors

Abstract

Global measures of peripheral blood DNA methylation have been associated with risk of some malignancies, including breast, bladder, and gastric cancer. Here, we examined genome-wide measures of peripheral blood DNA methylation in prostate cancer and its non-aggressive and aggressive disease forms.

DOI: 10.1002/pros.23289
PubMed: 28116812

Links to Exploration step

pubmed:28116812

Le document en format XML

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<term>DNA Methylation (physiology)</term>
<term>Genome-Wide Association Study (methods)</term>
<term>Humans</term>
<term>Male</term>
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<div type="abstract" xml:lang="en">Global measures of peripheral blood DNA methylation have been associated with risk of some malignancies, including breast, bladder, and gastric cancer. Here, we examined genome-wide measures of peripheral blood DNA methylation in prostate cancer and its non-aggressive and aggressive disease forms.</div>
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<Day>24</Day>
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<Year>2017</Year>
<Month>08</Month>
<Day>09</Day>
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<Year>2017</Year>
<Month>08</Month>
<Day>09</Day>
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<Volume>77</Volume>
<Issue>5</Issue>
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<Year>2017</Year>
<Month>Apr</Month>
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<Title>The Prostate</Title>
<ISOAbbreviation>Prostate</ISOAbbreviation>
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<ArticleTitle>Genome-Wide Measures of Peripheral Blood Dna Methylation and Prostate Cancer Risk in a Prospective Nested Case-Control Study.</ArticleTitle>
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<MedlinePgn>471-478</MedlinePgn>
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<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Global measures of peripheral blood DNA methylation have been associated with risk of some malignancies, including breast, bladder, and gastric cancer. Here, we examined genome-wide measures of peripheral blood DNA methylation in prostate cancer and its non-aggressive and aggressive disease forms.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">We used a matched, case-control study of 687 incident prostate cancer samples, nested within a larger prospective cohort study. DNA methylation was measured in pre-diagnostic, peripheral blood samples using the Illumina Infinium HM450K BeadChip. Genome-wide measures of DNA methylation were computed as the median M-value of all CpG sites and according to CpG site location and regulatory function. We used conditional logistic regression to test for associations between genome-wide measures of DNA methylation and risk of prostate cancer and its subtypes, and by time between blood draw and diagnosis.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">We observed no associations between the genome-wide measure of DNA methylation based on all CpG sites and risk of prostate cancer or aggressive disease. Risk of non-aggressive disease was associated with higher methylation of CpG islands (OR = 0.80; 95%CI = 0.68-0.94), promoter regions (OR = 0.79; 95%CI = 0.66-0.93), and high density CpG regions (OR = 0.80; 95%CI = 0.68-0.94). Additionally, higher methylation of all CpGs (OR = 0.66; 95%CI = 0.48-0.89), CpG shores (OR = 0.62; 95%CI = 0.45-0.84), and regulatory regions (OR = 0.68; 95% CI = 0.51-0.91) was associated with a reduced risk of overall prostate cancer within 5 years of blood draw but not thereafter.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">A reduced risk of overall prostate cancer within 5 years of blood draw and non-aggressive prostate cancer was associated with higher genome-wide methylation of peripheral blood DNA. While these data have no immediate clinical utility, with further work they may provide insight into the early events of prostate carcinogenesis. Prostate 77:471-478, 2017. © 2017 Wiley Periodicals, Inc.</AbstractText>
<CopyrightInformation>© 2017 Wiley Periodicals, Inc.</CopyrightInformation>
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<LastName>FitzGerald</LastName>
<ForeName>Liesel M</ForeName>
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<Affiliation>Cancer Epidemiology Centre, Cancer Council Victoria, Melbourne, VIC, Australia.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Cancer, Genetics, and Immunology, Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.</Affiliation>
</AffiliationInfo>
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<ForeName>Dallas R</ForeName>
<Initials>DR</Initials>
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<Affiliation>Cancer Epidemiology Centre, Cancer Council Victoria, Melbourne, VIC, Australia.</Affiliation>
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<AffiliationInfo>
<Affiliation>Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.</Affiliation>
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<Initials>G</Initials>
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<Affiliation>Cancer Epidemiology Centre, Cancer Council Victoria, Melbourne, VIC, Australia.</Affiliation>
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<AffiliationInfo>
<Affiliation>Université Paris-Saclay, University of Paris-Sud, UVSQ, CESP, INSERM, Villejuif, France.</Affiliation>
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<AffiliationInfo>
<Affiliation>Gustave Roussy, F-94805, Villejuif, France.</Affiliation>
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<AffiliationInfo>
<Affiliation>HuGeF, Human Genetics Foundation, Torino, Italy.</Affiliation>
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<LastName>Baglietto</LastName>
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<Initials>L</Initials>
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<Affiliation>Cancer Epidemiology Centre, Cancer Council Victoria, Melbourne, VIC, Australia.</Affiliation>
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<AffiliationInfo>
<Affiliation>Université Paris-Saclay, University of Paris-Sud, UVSQ, CESP, INSERM, Villejuif, France.</Affiliation>
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<Initials>J</Initials>
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<AffiliationInfo>
<Affiliation>Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.</Affiliation>
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<Affiliation>Genetic Epidemiology Laboratory, Department of Pathology, University of Melbourne, Parkville, VIC, Australia.</Affiliation>
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<Month>01</Month>
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<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
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<DescriptorName UI="D011471" MajorTopicYN="N">Prostatic Neoplasms</DescriptorName>
<QualifierName UI="Q000097" MajorTopicYN="Y">blood</QualifierName>
<QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
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<MeshHeading>
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</MeshHeadingList>
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<Keyword MajorTopicYN="N">DNA methylation</Keyword>
<Keyword MajorTopicYN="N">HM450K array</Keyword>
<Keyword MajorTopicYN="N">biomarker</Keyword>
<Keyword MajorTopicYN="N">peripheral blood</Keyword>
<Keyword MajorTopicYN="N">prostate cancer</Keyword>
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</MedlineCitation>
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<Month>08</Month>
<Day>30</Day>
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<PubMedPubDate PubStatus="accepted">
<Year>2016</Year>
<Month>11</Month>
<Day>11</Day>
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<Year>2017</Year>
<Month>1</Month>
<Day>25</Day>
<Hour>6</Hour>
<Minute>0</Minute>
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<Month>8</Month>
<Day>10</Day>
<Hour>6</Hour>
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<Month>1</Month>
<Day>25</Day>
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<PublicationStatus>ppublish</PublicationStatus>
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<ArticleId IdType="doi">10.1002/pros.23289</ArticleId>
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