Genetic and environmental factors in breast cancer
Genome analysis has identified several low penetrance breast cancer
loci but little is known about interactions between these loci and
environmental factors. Researchers in Oxford, England and Paris, France
have correlated environmental risk factors and 12 single nucleotide
polymorphisms (SNPs) known to be associated with breast cancer.
The study included 7,610 women with breast cancer, and 10,196 controls.
The 12 SNPs were correlated with 10 environmental risk factors (age at
menarche, parity, age at first birth, breastfeeding, menopausal
status, age at menopause, use of hormone replacement therapy [HRT],
BMI, height, and alcohol consumption). None of the 120 comparisons
showed evidence of gene-environment interaction. Use of HRT did not
affect genotypic relative risks either overall or for
oestrogen-receptor-positive breast cancer. Carriers of one high-risk
allele were significantly shorter than non-carriers.
This study showed no interaction between the 12 SNPs and the 10 environ*mental risk factors.Source: Medical Progress Related SubjectsPlatinum-Based Drugs in Cancer Therapy Gastric Cancer (Contemporary Issues in Cancer Imaging) Handbook of Evidence-Based Radiation Oncology - June 2010 EditionMesotheliomaMalignant Mesothelioma - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet ReferencesEndosurgery for Cancer (Vademecum)Surgical Oncology (Vademecum)The M.D. Anderson Surgical Oncology Handbook (Feig, M.D. Anderson Surgical Oncology Handbook)
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