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dc.contributor.authorLophatananon, A
dc.contributor.authorStewart-Brown, S
dc.contributor.authorKote-Jarai, Z
dc.contributor.authorOlama, AAA
dc.contributor.authorGarcia, SB
dc.contributor.authorNeal, DE
dc.contributor.authorHamdy, FC
dc.contributor.authorDonovan, JL
dc.contributor.authorGiles, GG
dc.contributor.authorFitzgerald, LM
dc.contributor.authorSouthey, MC
dc.contributor.authorPharoah, P
dc.contributor.authorPashayan, N
dc.contributor.authorGronberg, H
dc.contributor.authorWiklund, F
dc.contributor.authorAly, M
dc.contributor.authorStanford, JL
dc.contributor.authorBrenner, H
dc.contributor.authorDieffenbach, AK
dc.contributor.authorArndt, V
dc.contributor.authorPark, JY
dc.contributor.authorLin, H-Y
dc.contributor.authorSellers, T
dc.contributor.authorSlavov, C
dc.contributor.authorKaneva, R
dc.contributor.authorMitev, V
dc.contributor.authorBatra, J
dc.contributor.authorSpurdle, A
dc.contributor.authorClements, JA
dc.contributor.authorAPCB BioResource,
dc.contributor.authorPRACTICAL consortium,
dc.contributor.authorEaston, D
dc.contributor.authorEeles, RA
dc.contributor.authorMuir, K
dc.date.accessioned2017-11-01T16:02:11Z
dc.date.issued2017-08-22
dc.identifier.citationBritish journal of cancer, 2017, 117 (5), pp. 734 - 743
dc.identifier.issn0007-0920
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/894
dc.identifier.eissn1532-1827
dc.identifier.doi10.1038/bjc.2017.231
dc.description.abstractBACKGROUND: Evidence on height and prostate cancer risk is mixed, however, recent studies with large data sets support a possible role for its association with the risk of aggressive prostate cancer. METHODS: We analysed data from the PRACTICAL consortium consisting of 6207 prostate cancer cases and 6016 controls and a subset of high grade cases (2480 cases). We explored height, polymorphisms in genes related to growth processes as main effects and their possible interactions. RESULTS: The results suggest that height is associated with high-grade prostate cancer risk. Men with height >180 cm are at a 22% increased risk as compared to men with height <173 cm (OR 1.22, 95% CI 1.01-1.48). Genetic variants in the growth pathway gene showed an association with prostate cancer risk. The aggregate scores of the selected variants identified a significantly increased risk of overall prostate cancer and high-grade prostate cancer by 13% and 15%, respectively, in the highest score group as compared to lowest score group. CONCLUSIONS: There was no evidence of gene-environment interaction between height and the selected candidate SNPs.Our findings suggest a role of height in high-grade prostate cancer. The effect of genetic variants in the genes related to growth is seen in all cases and high-grade prostate cancer. There is no interaction between these two exposures.
dc.formatPrint-Electronic
dc.format.extent734 - 743
dc.languageeng
dc.language.isoeng
dc.publisherNATURE PUBLISHING GROUP
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectAPCB BioResource
dc.subjectPRACTICAL consortium
dc.subjectHumans
dc.subjectProstatic Neoplasms
dc.subjectBody Height
dc.subjectRisk Assessment
dc.subjectCase-Control Studies
dc.subjectPolymorphism, Single Nucleotide
dc.subjectAged
dc.subjectMiddle Aged
dc.subjectMale
dc.subjectNeoplasm Grading
dc.subjectGene-Environment Interaction
dc.titleHeight, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium.
dc.typeJournal Article
dcterms.dateAccepted2017-06-23
rioxxterms.versionofrecord10.1038/bjc.2017.231
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2017-08
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfBritish journal of cancer
pubs.issue5
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Oncogenetics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Oncogenetics
pubs.organisational-group/ICR/Students
pubs.organisational-group/ICR/Students/PhD and MPhil
pubs.organisational-group/ICR/Students/PhD and MPhil/18/19 Starting Cohort
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Oncogenetics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Oncogenetics
pubs.organisational-group/ICR/Students
pubs.organisational-group/ICR/Students/PhD and MPhil
pubs.organisational-group/ICR/Students/PhD and MPhil/18/19 Starting Cohort
pubs.publication-statusPublished
pubs.volume117
pubs.embargo.termsNot known
icr.researchteamOncogenetics
dc.contributor.icrauthorKote-Jarai, Zsofia
dc.contributor.icrauthorEeles, Rosalind


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