Genetic Variation in Steroid and Xenobiotic Metabolizing Pathways and Enterolactone Excretion Before and After Flaxseed Intervention in African American and European American Women

Cancer Epidemiol Biomarkers Prev. 2019 Feb;28(2):265-274. doi: 10.1158/1055-9965.EPI-18-0826.

Abstract

Background: Metabolism and excretion of the phytoestrogen enterolactone (ENL), which has been associated with breast cancer risk, may be affected by variation in steroid hormone and xenobiotic-metabolizing genes.

Methods: We conducted a randomized, crossover flaxseed intervention study in 252 healthy, postmenopausal women [137 European ancestry (EA) and 115 African ancestry (AA)] from western New York. Participants were randomly assigned to maintain usual diet or consume 10 g/day ground flaxseed for 6 weeks. After a 2-month washout period, participants crossed over to the other diet condition for an additional 6 weeks. Urinary ENL excretion was measured by gas chromatography-mass spectrometry and 70 polymorphisms in 29 genes related to steroid hormone and xenobiotic metabolism were genotyped. Mixed additive genetic models were constructed to examine association of genetic variation with urinary ENL excretion at baseline and after the flaxseed intervention.

Results: SNPs in several genes were nominally (P < 0.05) associated with ENL excretion at baseline and/or after intervention: ESR1, CYP1B1, COMT, CYP3A5, ARPC1A, BCL2L11, SHBG, SLCO1B1, and ZKSCAN5. A greater number of SNPs were associated among AA women than among EA women, and no SNPs were associated in both races. No SNP-ENL associations were statistically significant after correction for multiple comparisons.

Conclusions: Variation in several genes related to steroid hormone metabolism was associated with lignan excretion at baseline and/or after flaxseed intervention among postmenopausal women.

Impact: These findings may contribute to our understanding of the differences observed in urinary ENL excretion among AA and EA women and thus hormone-related breast cancer risk.

Publication types

  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural

MeSH terms

  • 4-Butyrolactone / analogs & derivatives*
  • 4-Butyrolactone / metabolism
  • 4-Butyrolactone / urine
  • Actin-Related Protein 2-3 Complex / genetics
  • Aged
  • Bcl-2-Like Protein 11 / genetics
  • Black or African American / genetics
  • Catechol O-Methyltransferase / genetics
  • Cross-Over Studies
  • Cytochrome P-450 CYP1B1 / genetics
  • Cytochrome P-450 CYP3A / genetics
  • DNA-Binding Proteins / genetics
  • Diet
  • Estrogen Receptor alpha / genetics
  • Female
  • Flax
  • Humans
  • Inactivation, Metabolic / genetics*
  • Lignans / metabolism
  • Lignans / urine*
  • Liver-Specific Organic Anion Transporter 1 / genetics
  • Middle Aged
  • Models, Genetic
  • Polymorphism, Single Nucleotide*
  • Postmenopause
  • Sex Hormone-Binding Globulin / genetics
  • Transcription Factors / genetics
  • White People / genetics

Substances

  • ARPC1A protein, human
  • Actin-Related Protein 2-3 Complex
  • BCL2L11 protein, human
  • Bcl-2-Like Protein 11
  • DNA-Binding Proteins
  • ESR1 protein, human
  • Estrogen Receptor alpha
  • Lignans
  • Liver-Specific Organic Anion Transporter 1
  • SHBG protein, human
  • SLCO1B1 protein, human
  • Sex Hormone-Binding Globulin
  • Transcription Factors
  • ZKSCAN5 protein, human
  • CYP1B1 protein, human
  • CYP3A5 protein, human
  • Cytochrome P-450 CYP1B1
  • Cytochrome P-450 CYP3A
  • COMT protein, human
  • Catechol O-Methyltransferase
  • 4-Butyrolactone
  • 2,3-bis(3'-hydroxybenzyl)butyrolactone