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Proteomic analysis of plasma proteins of workers exposed to benzene

Authors
Joo, WASuli, DLee, DYLee, ENKim, CW
Issue Date
14-3월-2004
Publisher
ELSEVIER
Keywords
benzene; comet assay; two-dimensional electrophoresis (2-DE); MALDI-TOF; TCR beta
Citation
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, v.558, no.1-2, pp.35 - 44
Indexed
SCIE
SCOPUS
Journal Title
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
Volume
558
Number
1-2
Start Page
35
End Page
44
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/123616
DOI
10.1016/j.mrgentox.2003.10.015
ISSN
1383-5718
Abstract
In this study, we analyzed the proteins in plasma of workers exposed to benzene by two-dimensional gel electrophoresis, in the hope of finding a specific protein suitable for the biomonitoring of benzene exposure. Comet assays were also carried out to evaluate lymphocytes DNA damage. Fifty workers from a printing company and 38 matched unexposed healthy subjects were enrolled in the study. DNA damage was found to be significantly higher in the exposed workers than in the controls. The tail moments of the two groups were 2.07 +/- 0.35 and 1.48 +/- 0.41, respectively (P < 0.0001). The mean values of trans, trans-muconic acid (t,t-MA) in workers exposed to benzene and in unexposed subjects were 1.011 +/- 0.249 and 0.026 +/- 0.028 mg/g creatinine, respectively. Protein profiles were significantly different (P < 0.05) in the two groups, as identified by matrix-assisted laser desorption ionization/time of flight (MALDI-TOF) mass spectrometry and confirmed by Western blot. T cell receptor beta chain (TCR beta), FK506-binding protein (FKBP51) and matrix metalloproteinase-l 3 (MMP13) were found to be up-regulated in the benzene-exposed workers. In addition, the correlation between TCR Pbeta and the tail moments of lymphocytes was statistically significant (r-value, 0.428). We conclude that TCR beta in plasma could be used for the early detection of exposure to benzene. (C) 2003 Elsevier B.V. All rights reserved.
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