Tumors arising from non-neural or glial tissue of the brain ('gliomas') constitute one of the most lethal human cancers. Few case-control studies of glioma have been undertaken, and the etiology of the tumor is largely unknown. However, the descriptive epidemiology of the disease, including an unexplained excess of glioma n the southeastern US, is consistent with an environmental component in the disease. Strong candidate risk factors, based on experimental evidence, include exposure to N-nitroso compounds (NOCs) in processed meats, and tobacco products, and consumption of alcohol. To shed light on the contribution of diet, genes and other potential risk factors to adult glioma, we are proposing a clinic-based, multi-institutional case- control study. Adults with a new diagnosis of glioma will be recruited from 5 treatment referral centers in the southeastern US. Subjects will be enrolled directly from clinics, generally within days or weeks of diagnosis. In the 5-year project, an estimated 1,200 persons with incident glioma and age- and gender-matched community controls will be enrolled in the study. Information on diet will be collected using a validated food frequency questionnaire, supplemented with a questionnaire developed by Sinha and colleagues at NCI designed specifically to measure NOCs and other meat carcinogens in the diet. In a structured interview, data will also be gathered on atopic immunity, and other exposures linked in past studies to glioma risk. To explore the contribution of genetic susceptibility, oral DNA samples will be collected from cases and controls, and whole genome amplification undertaken to augment the DNA for planned and future genotyping. Both candidate SNPs and haplotypes will be examined in a set of 31 proposed susceptibility genes involved in NOC metabolism, DNA repair and access of carcinogens to the CNS. With the large numbers available for analysis, the study will have power to investigate interactions of alcohol consumption and NOC exposure with the susceptibility genes in these pathways. The proposed study will be the largest US case-control study of glioma. Based in a high incidence region, the study may identify novel environmental risk factors and offer new insights on prevention and treatment for a leading fatal cancer in the US.
| Miller, Briana; Peeri, Noah C; Nabors, Louis Burt et al. (2018) Handedness and the risk of glioma. J Neurooncol 137:639-644 |
| Little, Rebecca B; Nabors, L Burt; Olson, Jeffrey J et al. (2017) Older age at the completion of linear growth is associated with an increased risk of adult glioma. Cancer Causes Control 28:709-716 |
| Egan, Kathleen M; Nabors, Louis B; Thompson, Zachary J et al. (2016) Analgesic use and the risk of primary adult brain tumor. Eur J Epidemiol 31:917-25 |
| Egan, Kathleen M; Baskin, Rebekah; Nabors, L Burton et al. (2015) Brain tumor risk according to germ-line variation in the MLLT10 locus. Eur J Hum Genet 23:132-4 |
| Baskin, Rebekah; Woods, Nicholas T; Mendoza-Fandiño, Gustavo et al. (2015) Functional analysis of the 11q23.3 glioma susceptibility locus implicates PHLDB1 and DDX6 in glioma susceptibility. Sci Rep 5:17367 |
| Anic, Gabriella M; Madden, Melissa H; Nabors, L Burton et al. (2014) Reproductive factors and risk of primary brain tumors in women. J Neurooncol 118:297-304 |
| Madden, Melissa H; Anic, Gabriella M; Thompson, Reid C et al. (2014) Circadian pathway genes in relation to glioma risk and outcome. Cancer Causes Control 25:25-32 |
| Amankwah, Ernest K; Thompson, Reid C; Nabors, L Burton et al. (2013) SWI/SNF gene variants and glioma risk and outcome. Cancer Epidemiol 37:162-5 |
| Little, Rebecca B; Madden, Melissa H; Thompson, Reid C et al. (2013) Anthropometric factors in relation to risk of glioma. Cancer Causes Control 24:1025-31 |
| Siegel, Erin M; Nabors, L Burton; Thompson, Reid C et al. (2013) Prediagnostic body weight and survival in high grade glioma. J Neurooncol 114:79-84 |
Showing the most recent 10 out of 19 publications
