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Verfasst von:Loveday, Chey [VerfasserIn]   i
 Sud, A. [VerfasserIn]   i
 Litchfield, K. [VerfasserIn]   i
 Levy, M. [VerfasserIn]   i
 Holroyd, A. [VerfasserIn]   i
 Broderick, P. [VerfasserIn]   i
 Kote‐Jarai, Z. [VerfasserIn]   i
 Dunning, A. M. [VerfasserIn]   i
 Muir, K. [VerfasserIn]   i
 Peto, J. [VerfasserIn]   i
 Eeles, R. [VerfasserIn]   i
 Easton, D. F. [VerfasserIn]   i
 Dudakia, D. [VerfasserIn]   i
 Orr, N. [VerfasserIn]   i
 Pashayan, N. [VerfasserIn]   i
 Reid, A. [VerfasserIn]   i
 Huddart, R. A. [VerfasserIn]   i
 Houlston, R. S. [VerfasserIn]   i
 Turnbull, C. [VerfasserIn]   i
 Brenner, Hermann [VerfasserIn]   i
Titel:Runs of homozygosity and testicular cancer risk
Verf.angabe:C. Loveday, A. Sud, K. Litchfield, M. Levy, A. Holroyd, P. Broderick, Z. Kote‐Jarai, A.M. Dunning, K. Muir, J. Peto, R. Eeles, D.F. Easton, D. Dudakia, N. Orr, N. Pashayan, A. Reid, R.A. Huddart, R.S. Houlston and C. Turnbull
E-Jahr:2019
Jahr:17-May-2019
Umfang:10 S.
Teil:volume:7
 year:2019
 number:4
 pages:555-564
 extent:10
Fussnoten:Appendix, Consortia, The UK Testicular Cancer Collaboration (UKTCC), Gordon Rustin [und weitere] ; Appendix, The PRACTICAL Consortium, Brian E. Henderson, ... Hermann Brenner [und weitere] ; Gesehen am 05.05.2020
Titel Quelle:Enthalten in: Andrology
Ort Quelle:Oxford [u.a.] : Wiley-Blackwell, 2013
Jahr Quelle:2019
Band/Heft Quelle:7(2019), 4, Seite 555-564
ISSN Quelle:2047-2927
Abstract:Background Testicular germ cell tumour (TGCT) is highly heritable but > 50% of the genetic risk remains unexplained. Epidemiological observation of greater relative risk to brothers of men with TGCT compared to sons has long alluded to recessively acting TGCT genetic susceptibility factors, but to date none have been reported. Runs of homozygosity (RoH) are a signature indicating underlying recessively acting alleles and have been associated with increased risk of other cancer types. Objective To examine whether RoH are associated with TGCT risk. Methods We performed a genome-wide RoH analysis using GWAS data from 3206 TGCT cases and 7422 controls uniformly genotyped using the OncoArray platform. Results Global measures of homozygosity were not significantly different between cases and controls, and the frequency of individual consensus RoH was not significantly different between cases and controls, after correction for multiple testing. RoH at three regions, 11p13-11p14.3, 5q14.1-5q22.3 and 13q14.11-13q.14.13, were, however, nominally statistically significant at p < 0.01. Intriguingly, RoH200 at 11p13-11p14.3 encompasses Wilms tumour 1 (WT1), a recognized cancer susceptibility gene with roles in sex determination and developmental transcriptional regulation, processes repeatedly implicated in TGCT aetiology. Discussion and conclusion Overall, our data do not support a major role in the risk of TGCT for recessively acting alleles acting through homozygosity, as measured by RoH in outbred populations of cases and controls.
DOI:doi:10.1111/andr.12667
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1111/andr.12667
 Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1111/andr.12667
 DOI: https://doi.org/10.1111/andr.12667
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:cancer
 genetics
 genome-wide association studies
 homozygosity mapping
 recessive
 runs of homozygosity
 testicular germ cell tumour
K10plus-PPN:1697202950
Verknüpfungen:→ Zeitschrift

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