1-Hydroxypyrene as Biomarker of Carcinogenesis in Steel Factory Workers

Jacek Belowski1 Roza Kubiak1, Jerzy Szczeklik1, Ewa Smolik2, Danuta Mielzynska2, Monika Baj1 and Anna Szczesna1

1 Department of Internal and Occupational Diseases, Medical School of Jagiellonian University, Krakow, Poland.
2 Institute of Occupational Medicine and Environmental Health, Sosnowiec, Poland.
 
Corresponding author: Jacek Belowski
Department of Internal and Occupational Diseases,
Medical School of Jagiellonian University.
Krakow ul. Sniadeckich 10,
Poland
Tel. (+48) 126 323 764
e-mail: mmbelows@cyf-kr.edu.pl

CEJOEM 1998; 4(3):280-287


Keywords:
Biomonitoring, polycyclic aromatic hydrocarbons, benzo(a)pyrene, occupational exposure, 1-hydroxypyrene, steel factory

Abbreviations:
1-HP = 1-hydroxypyrene
BaP = benzo(a)pyrene
HPLC = high pressure liquid chromatography
mg = microgram
mmol = mikromol

Abstract:
It is proved that various polycyclic hydrocarbons have major mutagenic and carcinogenic activity. The basis for research on the mechanism of mutagenic and carcinogenic activity of aromatic hydrocarbons was benzo(a)pyrene (BaP) – one of the most potent and most widespread carcinogens in human environment. In order to identify the persons particularly endangered, it is essential to establish the type and amount of the carcinogen absorbed, by evaluating concentrations of the carcinogen or its metabolites in body fluids, which leads to the identification of exposure markers. As biomarker of the absorbed dose of aromatic hydrocarbons the evaluation of urinary 1-hydroxypyrene (1-HP) is commonly used. Our study presents urinary 1-HP measurement in 82 steel-mill workers, of whom 56 were coke-oven department workers exposed to major concentrations of BaP, confirmed by environmental research. The mean, minimum and maximum 1-HP excretions after the end of work were 10.78 mmol/mol of creatinine, 0.61 mmol/mol of creatinine and 73.29 mmol/mol of creatinine, respectively. After three days a significant difference was found: the mean, maximum and minimum excretions were 1.50, 7.39 and 0.2, respectively. This indicates the possibility of using 1-HP excretion as biomarker of short-term exposure to aromatic hydrocarbons. 1-HP excretion falls rapidly after 3 days, thus 1-HP assessment can be used as a marker of exposure only when the material had been collected immediately after exposure. Minor influence of tobacco smoking on 1-HP excretion was found; it was not significant when compared to occupational exposure.


Received: 2 April 1998
Accepted: 22 July 1998

Posted: 19 November 1998

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