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Verfasst von:Yang, Yaohua [VerfasserIn]   i
 Wu, Lang [VerfasserIn]   i
 Shu, Xiao-Ou [VerfasserIn]   i
 Cai, Qiuyin [VerfasserIn]   i
 Shu, Xiang [VerfasserIn]   i
 Li, Bingshan [VerfasserIn]   i
 Guo, Xingyi [VerfasserIn]   i
 Ye, Fei [VerfasserIn]   i
 Michailidou, Kyriaki [VerfasserIn]   i
 Bolla, Manjeet K [VerfasserIn]   i
 Wang, Qin [VerfasserIn]   i
 Dennis, Joe [VerfasserIn]   i
 Andrulis, Irene L [VerfasserIn]   i
 Brenner, Hermann [VerfasserIn]   i
 Chenevix-Trench, Georgia [VerfasserIn]   i
 Campa, Daniele [VerfasserIn]   i
 Castelao, Jose E [VerfasserIn]   i
 Gago-Dominguez, Manuela [VerfasserIn]   i
 Dörk, Thilo [VerfasserIn]   i
 Hollestelle, Antoinette [VerfasserIn]   i
 Lophatananon, Artitaya [VerfasserIn]   i
 Muir, Kenneth [VerfasserIn]   i
 Neuhausen, Susan L [VerfasserIn]   i
 Olsson, Håkan [VerfasserIn]   i
 Sandler, Dale P [VerfasserIn]   i
 Simard, Jacques [VerfasserIn]   i
 Kraft, Peter [VerfasserIn]   i
 Pharoah, Paul D P [VerfasserIn]   i
 Easton, Douglas F [VerfasserIn]   i
 Zheng, Wei [VerfasserIn]   i
 Long, Jirong [VerfasserIn]   i
Titel:Genetically predicted levels of DNA methylation biomarkers and breast cancer risk
Titelzusatz:data from 228 951 women of European descent
Verf.angabe:Yaohua Yang, Lang Wu, Xiao-Ou Shu, Qiuyin Cai, Xiang Shu, Bingshan Li, Xingyi Guo, Fei Ye, Kyriaki Michailidou, Manjeet K. Bolla, Qin Wang, Joe Dennis, Irene L. Andrulis, Hermann Brenner, Georgia Chenevix-Trench, Daniele Campa, Jose E. Castelao, Manuela Gago-Dominguez, Thilo Dörk, Antoinette Hollestelle, Artitaya Lophatananon, Kenneth Muir, Susan L. Neuhausen, Håkan Olsson, Dale P. Sandler, Jacques Simard, Peter Kraft, Paul D.P. Pharoah, Douglas F. Easton, Wei Zheng, Jirong Long
Jahr:2020
Jahr des Originals:2019
Umfang:10 S.
Fussnoten:First published online May 29, 2019 ; Gesehen am 17.12.2020
Titel Quelle:Enthalten in: National Cancer InstituteJournal of the National Cancer Institute
Ort Quelle:Oxford : Oxford Univ. Press, 1941
Jahr Quelle:2020
Band/Heft Quelle:112(2020), 3, Seite 295-304
ISSN Quelle:1460-2105
Abstract:DNA methylation plays a critical role in breast cancer development. Previous studies have identified DNA methylation marks in white blood cells as promising biomarkers for breast cancer. However, these studies were limited by low statistical power and potential biases. Using a new methodology, we investigated DNA methylation marks for their associations with breast cancer risk.Statistical models were built to predict levels of DNA methylation marks using genetic data and DNA methylation data from HumanMethylation450 BeadChip from the Framingham Heart Study (n = 1595). The prediction models were validated using data from the Women’s Health Initiative (n = 883). We applied these models to genomewide association study (GWAS) data of 122 977 breast cancer patients and 105 974 controls to evaluate if the genetically predicted DNA methylation levels at CpG sites (CpGs) are associated with breast cancer risk. All statistical tests were two-sided.Of the 62 938 CpG sites CpGs investigated, statistically significant associations with breast cancer risk were observed for 450 CpGs at a Bonferroni-corrected threshold of P less than 7.94 × 10-7, including 45 CpGs residing in 18 genomic regions, that have not previously been associated with breast cancer risk. Of the remaining 405 CpGs located within 500 kilobase flaking regions of 70 GWAS-identified breast cancer risk variants, the associations for 11 CpGs were independent of GWAS-identified variants. Integrative analyses of genetic, DNA methylation, and gene expression data found that 38 CpGs may affect breast cancer risk through regulating expression of 21 genes.Our new methodology can identify novel DNA methylation biomarkers for breast cancer risk and can be applied to other diseases.
DOI:doi:10.1093/jnci/djz109
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/10.1093/jnci/djz109
 Volltext: https://academic.oup.com/jnci/article/112/3/295/5505447
 DOI: https://doi.org/10.1093/jnci/djz109
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1743111533
Verknüpfungen:→ Zeitschrift

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