© The Author 2008. Published by Oxford University Press.
Chromosome Translocations in Workers Exposed to Benzene
Affiliations of authors: School of Public Health, University of California, Berkeley, CA (CMH, CC, LZ, JDC, RT, MTS); Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD (QL, MS, NR); National Institute of Occupational Health and Poison Control, Chinese Center for Disease Control and Prevention, Beijing, China (GL, SY); Institute for Risk Assessment Sciences, Utrecht University, The Netherlands (RV); Roche Molecular Systems, Inc, Alameda, 1145 Atlantic Ave, Alameda, CA (RH)
Correspondence to: Martyn T. Smith, PhD, School of Public Health, 140 Warren Hall, University of California, Berkeley, CA 94720-7360 (e-mail: martynts{at}berkeley.edu).
As benzene has been linked with elevated risk of both acute myeloid leukemia and lymphoma, we explored the effect of benzene exposure on levels of t(8;21), t(15;17), and t(14;18) translocations. Circulating lymphocytes of normal individuals also often contain t(14;18). Quantitative polymerase chain reaction analysis showed that 37 workers with benzene exposure had a decreased level of t(14;18) in their blood with only 16.2% having 10 or more copies of the t(14;18) BCL-2/IgH fusion gene/µg DNA, as opposed to 55% of 20 controls (P = .0063 by Fishers exact test). This decline may be related to the immunotoxicity to specific subtypes of circulating B-lymphocytes, but the data do not support the use of t(14;18) as a biomarker of increased lymphoma risk in benzene-exposed populations. None of 88 individuals (31 controls and 57 exposed) exhibited detectable t(8;21) transcripts, and while t(15;17) transcripts were detected in two individuals, the result is inconclusive as one was exposed and the other was unexposed.
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