Decreased breast cancer risk in systemic lupus erythematosus: the search for a genetic basis continues

التفاصيل البيبلوغرافية
العنوان: Decreased breast cancer risk in systemic lupus erythematosus: the search for a genetic basis continues
المؤلفون: Rosalind Ramsey-Goldman, Caroline Gordon, Alison M. Dunning, Doug Easton, Ann E. Clarke, Kyriaki Michailidou, Sasha Bernatsky, William D. Foulkes
المصدر: Lupus. 21(8)
سنة النشر: 2012
مصطلحات موضوعية: Oncology, medicine.medical_specialty, Population, Single-nucleotide polymorphism, Genome-wide association study, Breast Neoplasms, Polymorphism, Single Nucleotide, White People, Breast cancer, Rheumatology, Risk Factors, Internal medicine, medicine, Odds Ratio, Humans, Lupus Erythematosus, Systemic, Genetic Predisposition to Disease, Allele, skin and connective tissue diseases, education, Alleles, education.field_of_study, business.industry, Cancer, Odds ratio, medicine.disease, Large breast, Immunology, Female, business, Genome-Wide Association Study
الوصف: Purpose: Recent work has demonstrated an important decrease in breast cancers for women with systemic lupus erythematosus (SLE). The reason behind this phenomenon is unknown. Our purpose was to explore whether the single nucleotide polymorphisms (SNPs) predisposing to SLE might be protective against breast cancer (in women in the general population). Methods: We focused on loci relevant to 10 SNPs associated with SLE (with a p value of −9). We determined whether we could establish a decreased frequency of these SNPs in breast cancer cases versus controls, within the general population. To do this we used a large breast cancer genome-wide association study (GWAS) dataset, involving 3,659 breast cancer cases and 4,897controls. These subjects were all primarily of European ancestry. Results: The population-based GWAS breast cancer data we examined suggested little evidence for important associations between breast cancer and SLE-related SNPs. Within the general population GWAS data, a cytosine(C) nucleotide substitution at rs9888739 (on chromosome 16p11.2) showed a very weak inverse association with breast cancer. The odds ratio (OR) for the rs9888739-C allele was 0.907551 ( p value 0.049899) in the GWAS breast cancer sample, compared to controls. There was a slightly stronger, positive, association with breast cancer for rs6445975-G (Guanine) on chromosome 3p14.3, with a breast cancer OR of 1.0911 ( p value 0.0097). Conclusions: Within this large breast cancer dataset, we did not demonstrate important associations with 10 lupus-associated SNPs. If decreased breast cancer risk in SLE is influenced by genetic profiles, this may be due to complex interactions and/or epigenetic factors.
تدمد: 1477-0962
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::097d4b4c62bc51aa24fdafe36f014592
https://pubmed.ncbi.nlm.nih.gov/22495874
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....097d4b4c62bc51aa24fdafe36f014592
قاعدة البيانات: OpenAIRE