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Associations of common variants in genes involved in metabolism and response to exogenous chemicals with risk of multiple myeloma
Journal article   Open access   Peer reviewed

Associations of common variants in genes involved in metabolism and response to exogenous chemicals with risk of multiple myeloma

Laura S. Gold, Anneclaire J. De Roos, Elizabeth E. Brown, Qing Lan, Kevin Milliken, Scott Davis, Stephen J. Chanock, Yawei Zhang, Richard Severson, Sheila H. Zahm, …
Cancer epidemiology, v 33(3-4), pp 276-280
01 Oct 2009
PMID: 19736056
url
https://europepmc.org/articles/pmc2808169View
Accepted (AM)Open Access (License Unspecified) Open

Abstract

Life Sciences & Biomedicine Oncology Public, Environmental & Occupational Health Science & Technology
Background: We examined risk of multiple myeloma (MM) associated with variants in genes involved in metabolism and response to exogenous chemicals [cytochrome P450 enzymes (CYP1B1, CYP20), epoxide hydrolase (EPHX1), paraoxonase 1 (PON1), arylhydrocarbon hydroxylase receptor (AHR), and NAD(P)H:quinone oxidoreductase (NQO1)]. Methods: This study included 279 MM cases and 782 controls in a pooled analysis of two population-based case-control studies. One common variant from each candidate gene was genotyped using DNA from blood or buccal cells. We estimated risk of MM associated with each genotype, controlling for race, gender, study site, and age, using odds ratios (OR) and 95% confidence intervals (CI). Results: Evaluations of the CYP1B1 V432L variant (rs1056836) suggested increased risk of MM among persons with the CG and GG genotypes compared to the CC genotype [OR (95% Cl) = 1.4 (1.0-2.0)]. Similar results were seen in analyses stratified by race and gender. We did not find any associations between MM and the CYP2C9, EPHX1, NQO1, or PON1 genes. Conclusions: CYP1B1 activates chemicals such as polycyclic aromatic hydrocarbons and dioxins to create oxidized, reactive intermediates, and higher gene activity has been shown for the G allele. We conducted the largest analysis to date on MM and these genetic variants and our results provide preliminary evidence that variation in CYP1B1 may influence susceptibility to MM. (C) 2009 Elsevier Ltd. All rights reserved.

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Collaboration types
Domestic collaboration
Web of Science research areas
Oncology
Public, Environmental & Occupational Health
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