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Functional polymorphisms in the TERT promoter are associated with risk of serous epithelial ovarian and breast cancers
Authors:Beesley Jonathan  Pickett Hilda A  Johnatty Sharon E  Dunning Alison M  Chen Xiaoqing  Li Jun  Michailidou Kyriaki  Lu Yi  Rider David N  Palmieri Rachel T  Stutz Michael D  Lambrechts Diether  Despierre Evelyn  Lambrechts Sandrina  Vergote Ignace  Chang-Claude Jenny  Nickels Stefan  Vrieling Alina  Flesch-Janys Dieter  Wang-Gohrke Shan  Eilber Ursula  Bogdanova Natalia  Antonenkova Natalia  Runnebaum Ingo B  Dörk Thilo  Goodman Marc T  Lurie Galina  Wilkens Lynne R  Matsuno Rayna K  Kiemeney Lambertus A  Aben Katja K H  Marees Tamara  Massuger Leon F A G  Fridley Brooke L  Vierkant Robert A  Bandera Elisa V  Olson Sara H
Affiliation:Division of Genetics and Population Health, Queensland Institute of Medical Research, Brisbane, Queensland, Australia. jonathan.beesley@qimr.edu.au
Abstract:Genetic variation at the TERT-CLPTM1L locus at 5p15.33 is associated with susceptibility to several cancers, including epithelial ovarian cancer (EOC). We have carried out fine-mapping of this region in EOC which implicates an association with a single nucleotide polymorphism (SNP) within the TERT promoter. We demonstrate that the minor alleles at rs2736109, and at an additional TERT promoter SNP, rs2736108, are associated with decreased breast cancer risk, and that the combination of both SNPs substantially reduces TERT promoter activity.
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