IL10 and TNF variants and risk of non-Hodgkin lymphoma among three Asian populations |
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Authors: | H. Dean Hosgood III Wing-Yan Au Hee Nam Kim Jie Liu Wei Hu Jovic Tse Bao Song Kit-fai Wong Je-Jung Lee Stephen J. Chanock L. P. Siu Mark P. Purdue Min-ho Shin Jinming Yu Raymond Liang Hyeoung-Joon Kim Nathaniel Rothman Qing Lan |
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Affiliation: | 1. Division of Cancer Epidemiology and Genetics, NCI, NIH, DHHS, Bethesda, MD, USA 2. Division of Epidemiology, Department of Epidemiology and Population Health, Albert Einstein College of Medicine, 1300 Morris Park Ave., Belfer 1309, Bronx, NY, 10461, USA 3. Department of Medicine, Queen Mary Hospital, University of Hong Kong, Hong Kong, Hong Kong 4. Genome Research Center for Hematopoietic Diseases, Chonnam National University Hwasun Hospital, Hwasun, Jeollanam-do, South Korea 5. Key Laboratory of Radiation Oncology of Shandong Province, Shandong Cancer Hospital and Institute, Jinan, Shandong, China 6. Department of Pathology, Queen Elizabeth Hospital, Hong Kong, Hong Kong 7. Department of Hematology/Oncology, Research Institute of Medical Sciences, Chonnam National University Medical School, Gwangju, South Korea 8. Department of Preventive Medicine, Chonnam National University Medical School, Gwangju, South Korea
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Abstract: | Genetic variation in immune-related genes, such as IL10 and TNF, have been associated with the development of non-Hodgkin lymphoma (NHL) in Caucasian populations. To test the hypothesis that IL10 and TNF polymorphisms may be associated with NHL risk in Asian populations, we genotyped 20 single nucleotide polymorphisms (SNPs) within the IL10 and TNF/LTA loci in three independent case–control studies (2635 cases and 4234 controls). IL10 rs1800871, rs1800872, and rs1800896 were genotyped in all three studies, while 5 of the remaining SNPs were genotyped in two studies, and 12 in a single study. IL10 rs1800896 was associated with B cell lymphoma [per-allele odds ratio (OR) = 1.25, 95 % confidence interval (CI) 1.08–1.45; p trend = 0.003], specifically diffuse large B cell lymphoma (DLBCL) (per-allele OR = 1.29, 95 % CI 1.08–1.53; p trend = 0.004), as well as T cell lymphoma (per-allele OR = 1.44, 95 % CI 1.13–1.82; p trend = 0.003). TNF rs1800629, which was genotyped in only two of our studies, was also associated with B cell lymphoma (per-allele OR = 0.77, 95 % CI 0.64–0.91; p trend = 0.003), specifically DLBCL (per-allele OR = 0.69, 95 % CI 0.55–0.86; p trend = 0.001). Our findings suggest that genetic variation in IL10 and TNF may also play a role in lymphomagenesis in Asian populations. |
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