CEBP Grants Frontiers in Basic Cancer Research
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

Cancer Epidemiology Biomarkers & Prevention 16, 1098, June 1, 2007. doi: 10.1158/1055-9965.EPI-06-0639
© 2007 American Association for Cancer Research

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Novik, K. L.
Right arrow Articles by Brooks-Wilson, A. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Novik, K. L.
Right arrow Articles by Brooks-Wilson, A. R.

Genetic Variation in H2AFX Contributes to Risk of Non–Hodgkin Lymphoma

Karen L. Novik1, John J. Spinelli2,5, Amy C. MacArthur2, Karey Shumansky2, Payal Sipahimalani1, Stephen Leach1, Agnes Lai2, Joseph M. Connors3,6, Randy D. Gascoyne4,7, Richard P. Gallagher2,5 and Angela R. Brooks-Wilson1,8

1 Genome Sciences Centre and 2 Cancer Control Research, British Columbia Cancer Research Centre; Departments of 3 Medical Oncology and 4 Pathology and Laboratory Medicine, British Columbia Cancer Agency; Departments of 5 Healthcare and Epidemiology, 6 Oncology, 7 Laboratory Medicine, and 8 Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada

Requests for reprints: Angela R. Brooks-Wilson, Genome Sciences Centre, British Columbia Cancer Research Centre, 675 West 10th Avenue, Room 7-111, Vancouver, British Columbia, Canada V5Z 1L3. Phone: 604-675-8156; Fax: 604-675-8178. E-mail: abrooks-wilson{at}bcgsc.ca

Non–Hodgkin lymphoma (NHL) comprises a group of lymphoid tumors that have in common somatic translocations. H2AFX encodes a key histone involved in the detection of the DNA double-stranded breaks that can lead to translocations. H2afx is a dosage-dependent gene that protects against B-cell lymphomas in mice, making its human orthologue an ideal candidate gene for susceptibility to lymphoma. We did a population-based genetic association study of H2AFX variants in 487 NHL cases and 531 controls. Complete resequencing of the human H2AFX gene in 95 NHL cases was done to establish the spectrum of variation in affected individuals; this was followed by both direct and indirect tests for association at the level of individual single nucleotide polymorphisms (SNP) and as haplotypes. Homozygosity for the AA genotype of a SNP 417 bp upstream of the translational start of H2AFX is strongly associated [odds ratio (OR), 0.54; P = 0.001] with protection from NHL. We find a strong association of this SNP with the follicular lymphoma subtype of NHL (AA genotype: OR, 0.40; P = 0.004) and with mantle cell lymphoma (AA genotype: OR, 0.20; P = 0.01) that remains significant after adjustment for the false discovery rate, but not with diffuse large B-cell lymphoma. These data support the hypothesis that genetic variation in the H2AFX gene influences genetic susceptibility or resistance to some subtypes of NHL by contributing to the maintenance of genome stability. (Cancer Epidemiol Biomarkers Prev 2007;16(6):1098–106)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2007 by the American Association for Cancer Research.