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Gene expression in benzene-exposed workers by microarray analysis of peripheral mononuclear blood cells: induction and silencing of CYP4F3A and regulation of DNA-dependent protein kinase catalytic subunit in DNA double strand break repair.

Authors
Bi-Y; Li-Y; Kong-M; Xiao-X; Zhao-Z; He-X; Ma-Q
Source
Chem-Biol Interact 2010 Mar; 184(1-2):207-211
Link
NIOSHTIC No.
20036676
Abstract
Benzene causes hematotoxicity and leukemia in humans. To analyze benzene-caused aberrant gene expression, we examined differential gene expression by microarray analysis of peripheral mononuclear blood cells from seven workers diagnosed with benzene poisoning and seven matched controls. Twenty-two genes were found up-regulated and 18 down-regulated in benzene patients compared with controls. Here we report the characterization of two benzene-regulated genes. CYP4F3A, which encodes the leukotriene B4 (LTB4) omega-hydroxylase, is important for inactivation of LTB4 in neutrophils. CYP4F3A mRNA was found elevated in all patients; moreover, CYP4F3A mRNA and protein were induced by benzene metabolite phenol in HL-60 and K562 cells as well as ex vivo in human peripheral neutrophils. Silencing of CYP4F3A in HL-60 cells by lentiviral delivery of CYP4F3A-specific siRNA reduced cell survival to 56%, 44%, 22%, 14%, and 3% at 3, 4, 5, 6, and 7 days, respectively; the results suggest that CYP4F3A is a critical positive regulator of HL-60 proliferation. DNA-dependent protein kinase catalytic subunit (DNAPKcs) regulates non-homologous end joining (NHEJ) in DNA double strand break (DSB) repair. DNA-PKcs mRNA was found consistently increased in the patients and DNA-PKcs mRNA and protein were induced by hydroquinone in HL-60 cells. In a DSB model, hydroquinone induced the formation of gamma-H2AX foci, a marker of DSBs, in HL-60 cells. The findings indicate that hydroquinone induces DSBs and induction correlates with elevated levels of DNA-PKcs and NHEJ. Similar results were obtained in K562 cells treated with phenol. Since NHEJ is error-prone, induction of DNA-PKcs and NHEJ may contribute to mutagenesis and leukemia by benzene. To our knowledge, the study demonstrated for the first time that benzene and metabolites induce CYP4F3A and DNA-PKcs both in vivo and in vitro. Induction of the genes may play a role in the pathogenesis of benzene hematotoxicity and serve as biomarkers of benzene exposure.
Keywords
Benzenes; Benzene-poisoning; Gene-mutation; Genes; Genotoxic-effects; Genotoxicity; Solvents; Organic-solvents; Mutagens; Mutagenicity; Mutation; Mutagenesis; Author Keywords: Benzene; Microarray; CYP4F3; DNA-PKcs; DNA double strand break repair
Contact
Yongyi Bi, School of Public Health, Wuhan University, 185 Donghu Rd., Wuhan, Hubei 430071, China
CODEN
CBINA8
CAS No.
71-43-2
Publication Date
20100319
Document Type
Journal Article
Email Address
yongyib@yahoo.com.cn
Fiscal Year
2010
NTIS Accession No.
NTIS Price
Issue of Publication
1-2
ISSN
0009-2797
NIOSH Division
HELD
Priority Area
Manufacturing
Source Name
Chemico-Biological Interactions
State
WV
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