Inherited variants in mitochondrial biogenesis genes may influence epithelial ovarian cancer risk.

Journal Article (Journal Article;Multicenter Study)

BACKGROUND: Mitochondria contribute to oxidative stress, a phenomenon implicated in ovarian carcinogenesis. We hypothesized that inherited variants in mitochondrial-related genes influence epithelial ovarian cancer (EOC) susceptibility. METHODS: Through a multicenter study of 1,815 Caucasian EOC cases and 1,900 controls, we investigated associations between EOC risk and 128 single nucleotide polymorphisms (SNPs) from 22 genes/regions within the mitochondrial genome (mtDNA) and 2,839 nuclear-encoded SNPs localized to 138 genes involved in mitochondrial biogenesis (BIO, n = 35), steroid hormone metabolism (HOR, n = 13), and oxidative phosphorylation (OXP, n = 90) pathways. Unconditional logistic regression was used to estimate OR and 95% CI between genotype and case status. Overall significance of each gene and pathway was evaluated by using Fisher's method to combine SNP-level evidence. At the SNP level, we investigated whether lifetime ovulation, hormone replacement therapy (HRT), and cigarette smoking were confounders or modifiers of associations. RESULTS: Interindividual variation involving BIO was most strongly associated with EOC risk (empirical P = 0.050), especially for NRF1, MTERF, PPARGC1A, ESRRA, and CAMK2D. Several SNP-level associations strengthened after adjustment for nongenetic factors, particularly for MTERF. Statistical interactions with cigarette smoking and HRT use were observed with MTERF and CAMK2D SNPs, respectively. Overall variation within mtDNA, HOR, and OXP was not statistically significant (empirical P > 0.10). CONCLUSION: We provide novel evidence to suggest that variants in mitochondrial biogenesis genes may influence EOC susceptibility. IMPACT: A deeper understanding of the complex mechanisms implicated in mitochondrial biogenesis and oxidative stress may aid in developing strategies to reduce morbidity and mortality from EOC.

Full Text

Duke Authors

Cited Authors

  • Permuth-Wey, J; Chen, YA; Tsai, Y-Y; Chen, Z; Qu, X; Lancaster, JM; Stockwell, H; Dagne, G; Iversen, E; Risch, H; Barnholtz-Sloan, J; Cunningham, JM; Vierkant, RA; Fridley, BL; Sutphen, R; McLaughlin, J; Narod, SA; Goode, EL; Schildkraut, JM; Fenstermacher, D; Phelan, CM; Sellers, TA

Published Date

  • June 2011

Published In

Volume / Issue

  • 20 / 6

Start / End Page

  • 1131 - 1145

PubMed ID

  • 21447778

Pubmed Central ID

  • PMC3111851

Electronic International Standard Serial Number (EISSN)

  • 1538-7755

Digital Object Identifier (DOI)

  • 10.1158/1055-9965.EPI-10-1224


  • eng

Conference Location

  • United States