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Induction of CYP4F3 by benzene metabolites in human white blood cells in vivo, in human promyelocytic leukemic cell lines, and ex vivo in human blood neutrophils.

Authors
Zhao-Z; He-X; Bi-Y; Xia-Y; Tao-N; Li-L; Ma-Q
Source
Drug Metab Dispos 2009 Feb; 37(2):282-291
NIOSHTIC No.
20034763
Abstract
Exposure to benzene elicits a spectrum of hematotoxicity ranging from reduction of peripheral blood cell counts to aplastic anemia and leukemia. The molecular mechanism by which benzene damages hematopoietic cells is unclear; in particular, benzene-induced aberrant gene expression has not been addressed. We analyzed differential gene expression in the peripheral white blood cells (WBC) from 7 female patients diagnosed with occupational benzene poisoning and 7 matched controls. Here, we report altered expression of cytochrome P450 (CYP) in the patients. All patients exhibited elevated expression of CYP4F3A encoding the leukotriene B4 (LTB4) -hydroxylase critical in the inactivation of LTB4 in polymorphonuclear leukocytes (PMN) with a fold of induction between 3 and 71. Four patients had high expression of CYP1A1 and two patients had elevated expression of CYP1B1. Expressions of CYP2B6, CYP51, and CYP27A1 were also altered in certain patients. Mechanistic analysis revealed that phenol, a major metabolite of benzene, significantly induced the expression of CYP4F3A at both mRNA and protein levels in cultured promyelocytic leukemia cells (HL-60) similarly to all-trans retinoic acid (ATRA). Induction of CYP4F3 by phenol was also observed in differentiated HL-60 cells, in pro-erythroid cell line K562, and ex vivo in human neutrophiles. On the other hand, hydroquinone induced extensive apoptosis of the cells. The findings demonstrated, for the first time, that benzene and metabolites induce CYP4F3 in human blood cells both in vivo and in vitro. Induction of CYP4F3 may play a role in the development of benzene hematotoxicity and serve as a biomarker of benzene exposure.
Keywords
Cell-biology; Cell-function; Cellular-reactions; Biochemical-analysis; Biochemistry; Biological-effects; Biological-transport; Blood-cells; Blood-disorders; Blood-tests; Genes; Genetic-factors; Chemical-hypersensitivity; Chemical-synthesis; Occupational-exposure; Poisons; Toxic-effects; Toxicology; Toxicopathology; Benzene-poisoning; Molecular-biology
Contact
Qiang Ma, National Institute for Occupational Safety and Health, CDC, Receptor Biology Laboratory, TMBB, HELD, MS 3014, 1095 Willowdale Road, Morgantown, WV 26505
CODEN
DMDSAI
CAS No.
71-43-2
Publication Date
20090201
Document Type
Journal Article
Email Address
qam1@cdc.gov
Fiscal Year
2009
NTIS Accession No.
NTIS Price
Issue of Publication
2
ISSN
0090-9556
NIOSH Division
HELD
Source Name
Drug Metabolism and Disposition
State
WV
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