1. APOBEC3A/B deletion polymorphism and cancer risk
- Author
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Paal Romundstad, Serena Nik-Zainal, Per Eystein Lønning, Stian Knappskog, Liv Beathe Gansmo, Lars J. Vatten, Kristian Hveem, Nik-Zainal Abidin, Serena [0000-0001-5054-1727], and Apollo - University of Cambridge Repository
- Subjects
0301 basic medicine ,Oncology ,APOBEC ,Adult ,Male ,Cancer Research ,medicine.medical_specialty ,Genotype ,Colorectal cancer ,Population ,Germline ,White People ,Minor Histocompatibility Antigens ,03 medical and health sciences ,Prostate cancer ,0302 clinical medicine ,Risk Factors ,Internal medicine ,Cytidine Deaminase ,Neoplasms ,medicine ,Humans ,Genetic Predisposition to Disease ,education ,Lung cancer ,Cancer Biomarkers and Molecular Epidemiology ,Aged ,education.field_of_study ,Polymorphism, Genetic ,business.industry ,Norway ,Case-control study ,Proteins ,General Medicine ,respiratory system ,Middle Aged ,medicine.disease ,humanities ,3. Good health ,030104 developmental biology ,030220 oncology & carcinogenesis ,Case-Control Studies ,Female ,business - Abstract
The germline ‘APOBEC3A/B’ deletion polymorphism, previously linked to APOBEC-dependent mutational signatures, was found associated with lung cancer risk among young individuals and age at diagnosis for lung and prostate cancer. No associations were found to breast or colon cancer., Activity of the apolipoprotein B mRNA editing enzyme, catalytic-polypeptide-like (APOBEC) enzymes has been linked to specific mutational processes in human cancer genomes. A germline APOBEC3A/B deletion polymorphism is associated with APOBEC-dependent mutational signatures, and the deletion allele has been reported to confer an elevated risk of some cancers in Asian populations, while the results in European populations, so far, have been conflicting. We genotyped the APOBEC3A/B deletion polymorphism in a large population-based sample consisting of 11 106 Caucasian (Norwegian) individuals, including 7279 incident cancer cases (1769 breast, 1360 lung, 1585 colon, and 2565 prostate cancer) and a control group of 3827 matched individuals without cancer (1918 females and 1909 males) from the same population. Overall, the APOBEC3A/B deletion polymorphism was not associated with risk of any of the four cancer types. However, in subgroup analyses stratified by age, we found that the deletion allele was associated with increased risk for lung cancer among individuals
- Published
- 2017