Publication

Genetic studies of a cluster of acute lymphoblastic leukemia cases in Churchill County, Nevada

Downloadable Content

Persistent URL
Last modified
  • 05/15/2025
Type of Material
Authors
    Karen K. Steinberg, Centers for Disease Control and PreventionMary V. Relling, St. Jude Children’s Research HospitalMargaret L. Gallagher, Centers for Disease Control and PreventionChristopher N. Greene, Centers for Disease Control and PreventionCarol S. Rubin, Centers for Disease Control and PreventionDeborah French, St. Jude Children’s Research HospitalAdrianne K. Holmes, Centers for Disease Control and PreventionWilliam L. Carroll, New York UniversityDeborah A. Koontz, Centers for Disease Control and PreventionEric J. Sampson, Centers for Disease Control and PreventionGlen Satten, Emory University
Language
  • English
Date
  • 2007-01-01
Publisher
  • National Institute of Environmental Health Sciences (NIEHS)
Publication Version
Copyright Statement
  • Publication of EHP lies in the public domain and is therefore without copyright
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0091-6765
Volume
  • 115
Issue
  • 1
Start Page
  • 158
End Page
  • 164
Grant/Funding Information
  • This work was supported by National Cancer Institute grant CA 51001 and National Institutes of Health grant CA21765; by a Center of Excellence grant from the State of Tennessee; and by American Lebanese Syrian Associated Charities.
Abstract
  • Objective: In a study to identify exposures associated with 15 cases of childhood leukemia, we found levels of tungsten, arsenic, and dichlorodiphenyldichloroethylene in participants to be higher than mean values reported in the National Report on Human Exposure to Environmental Chemicals. Because case and comparison families had similar levels of these contaminants, we conducted genetic studies to identify gene polymorphisms that might have made case children more susceptible than comparison children to effects of the exposures. Design: We compared case with comparison children to determine whether differences existed in the frequency of polymorphic genes, including genes that code for enzymes in the folate and purine pathways. We also included discovery of polymorphic forms of genes that code for enzymes that are inhibited by tungsten: xanthine dehydrogenase, sulfite oxidase (SUOX gene), and aldehyde oxidase. Participants: Eleven case children were age- and sex-matched with 42 community comparison children for genetic analyses. Twenty parents of case children also contributed to the analyses. Results: One bilalleleic gene locus in SUOX was significantly associated with either case or comparison status, depending on which alleles the child carried (without adjusting for multiple comparisons). Conclusions: Although genetic studies did not provide evidence that a common agent or genetic susceptibility factor caused the leukemias, the association between a SUOX gene locus and disease status in the presence of high tungsten and arsenic levels warrants further investigation. Relevance: Although analyses of community clusters of cancer have rarely identified causes, these findings have generated hypotheses to be tested in subsequent studies.
Author Notes
  • Address correspondence to K. Steinberg, Coordinating Center for Health Promotion, 2877 Brandywine Rd., Mailstop-K88, Koger Center, Williams Building, Room 3809, Chamblee, GA 30341 USA. Telephone: (770) 488-6067. Fax: (770) 488-6448. E-mail: kks1@cdc.gov
Keywords
Research Categories
  • Health Sciences, Public Health
  • Biology, Ecology
  • Biology, Genetics

Tools

Relations

In Collection:

Items