Skip to main content
Occupational and Environmental Medicine logoLink to Occupational and Environmental Medicine
. 1995 Nov;52(11):750–756. doi: 10.1136/oem.52.11.750

Evaluation of biomarkers in plasma, blood, and urine samples from coke oven workers: significance of exposure to polycyclic aromatic hydrocarbons.

S Ovrebø 1, A Haugen 1, P B Farmer 1, D Anderson 1
PMCID: PMC1128356  PMID: 8535495

Abstract

OBJECTIVE--The aim was to assess the significance of two biomarkers; antibody to benzo(a)pyrene DNA adducts and concentration of hydroxyethylvaline haemoglobin adducts in samples from a well studied group of coke oven workers. As a measure of exposure we have used 1-hydroxypyrene in urine. METHODS--Urine and blood samples were collected from coke oven workers and a control group. Samples from coke oven plant workers were collected in January and June. 1-Hydroxypyrene was measured in urine by high performance liquid chromatography (HPLC), antibodies to benzo(a)pyrene DNA adducts were measured by ELISA and hydroxyethylvaline haemoglobin adducts were measured by gas chromatography-mass spectrometry (GC-MS). RESULTS--Mean urinary 1-hydroxypyrene in samples from coke oven workers varied from 1.11 to 5.53 umol/mol creatinine and 0.14 umol/mol creatinine in the control group. Workers at the top side had the highest values of urinary 1-hydroxypyrene. Antibody to benzo(a)pyrene DNA adducts did not correlate with either 1-hydroxypyrene nor length of work at the coke oven plant. But antibody concentration in samples collected in January was predictive of the concentration in samples collected in June. A small non-significant increase in hydroxyethylvaline haemoglobin adducts was found in samples from coke oven workers relative to the control group when comparing smokers and nonsmokers separately. CONCLUSION--1-Hydroxypyrene correlates well with exposure groups based on job description. Antibodies to benzo(a)-pyrene DNA adducts was related to people and not exposure. Work at a coke oven plant might lead to increased hydroxyethylvaline haemoglobin adducts.

Full text

PDF
750

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bailey E., Brooks A. G., Dollery C. T., Farmer P. B., Passingham B. J., Sleightholm M. A., Yates D. W. Hydroxyethylvaline adduct formation in haemoglobin as a biological monitor of cigarette smoke intake. Arch Toxicol. 1988;62(4):247–253. doi: 10.1007/BF00332482. [DOI] [PubMed] [Google Scholar]
  2. Bailey E., Farmer P. B., Tang Y. S., Vangikar H., Gray A., Slee D., Ings R. M., Campbell D. B., McVie J. G., Dubbelman R. Hydroxyethylation of hemoglobin by 1-(2-chloroethyl)-1-nitrosoureas. Chem Res Toxicol. 1991 Jul-Aug;4(4):462–466. doi: 10.1021/tx00022a010. [DOI] [PubMed] [Google Scholar]
  3. Beach A. C., Gupta R. C. Human biomonitoring and the 32P-postlabeling assay. Carcinogenesis. 1992 Jul;13(7):1053–1074. doi: 10.1093/carcin/13.7.1053. [DOI] [PubMed] [Google Scholar]
  4. Beland F. A., Poirier M. C. Significance of DNA adduct studies in animal models for cancer molecular dosimetry and risk assessment. Environ Health Perspect. 1993 Mar;99:5–10. doi: 10.1289/ehp.93995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Farmer P. B., Bailey E., Gorf S. M., Törnqvist M., Osterman-Golkar S., Kautiainen A., Lewis-Enright D. P. Monitoring human exposure to ethylene oxide by the determination of haemoglobin adducts using gas chromatography-mass spectrometry. Carcinogenesis. 1986 Apr;7(4):637–640. doi: 10.1093/carcin/7.4.637. [DOI] [PubMed] [Google Scholar]
  6. Farmer P. B., Bailey E., Naylor S., Anderson D., Brooks A., Cushnir J., Lamb J. H., Sepai O., Tang Y. S. Identification of endogenous electrophiles by means of mass spectrometric determination of protein and DNA adducts. Environ Health Perspect. 1993 Mar;99:19–24. doi: 10.1289/ehp.939919. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Ferreira M., Jr, Buchet J. P., Burrion J. B., Moro J., Cupers L., Delavignette J. P., Jacques J., Lauwerys R. Determinants of urinary thioethers, D-glucaric acid and mutagenicity after exposure to polycyclic aromatic hydrocarbons assessed by air monitoring and measurement of 1-hydroxypyrene in urine: a cross-sectional study in workers of coke and graphite-electrode-producing plants. Int Arch Occup Environ Health. 1994;65(5):329–338. doi: 10.1007/BF00405698. [DOI] [PubMed] [Google Scholar]
  8. Gaylor D. W., Kadlubar F. F., Beland F. A. Application of biomarkers to risk assessment. Environ Health Perspect. 1992 Nov;98:139–141. doi: 10.1289/ehp.9298139. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Grammer L. C., Shaughnessy M. A., Davis R. A. Exposure to TMXDI (meta) aliphatic isocyanate and TMI (meta) unsaturated aliphatic isocyanate. Clinical and immunological evaluation of 96 workers. J Occup Med. 1993 Mar;35(3):287–290. [PubMed] [Google Scholar]
  10. Harris C. C., Vahakangas K., Newman M. J., Trivers G. E., Shamsuddin A., Sinopoli N., Mann D. L., Wright W. E. Detection of benzo[a]pyrene diol epoxide-DNA adducts in peripheral blood lymphocytes and antibodies to the adducts in serum from coke oven workers. Proc Natl Acad Sci U S A. 1985 Oct;82(19):6672–6676. doi: 10.1073/pnas.82.19.6672. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Haugen A., Becher G., Benestad C., Vahakangas K., Trivers G. E., Newman M. J., Harris C. C. Determination of polycyclic aromatic hydrocarbons in the urine, benzo(a)pyrene diol epoxide-DNA adducts in lymphocyte DNA, and antibodies to the adducts in sera from coke oven workers exposed to measured amounts of polycyclic aromatic hydrocarbons in the work atmosphere. Cancer Res. 1986 Aug;46(8):4178–4183. [PubMed] [Google Scholar]
  12. Herikstad B. V., Ovrebø S., Haugen A., Hagen I. Determination of polycyclic aromatic hydrocarbons in urine from coke-oven workers with a radioimmunoassay. Carcinogenesis. 1993 Feb;14(2):307–309. doi: 10.1093/carcin/14.2.307. [DOI] [PubMed] [Google Scholar]
  13. Jongeneelen F. J., Anzion R. B., Henderson P. T. Determination of hydroxylated metabolites of polycyclic aromatic hydrocarbons in urine. J Chromatogr. 1987 Jan 23;413:227–232. doi: 10.1016/0378-4347(87)80230-x. [DOI] [PubMed] [Google Scholar]
  14. Jongeneelen F. J., Anzion R. B., Scheepers P. T., Bos R. P., Henderson P. T., Nijenhuis E. H., Veenstra S. J., Brouns R. M., Winkes A. 1-Hydroxypyrene in urine as a biological indicator of exposure to polycyclic aromatic hydrocarbons in several work environments. Ann Occup Hyg. 1988;32(1):35–43. doi: 10.1093/annhyg/32.1.35. [DOI] [PubMed] [Google Scholar]
  15. Jongeneelen F. J., van Leeuwen F. E., Oosterink S., Anzion R. B., van der Loop F., Bos R. P., van Veen H. G. Ambient and biological monitoring of cokeoven workers: determinants of the internal dose of polycyclic aromatic hydrocarbons. Br J Ind Med. 1990 Jul;47(7):454–461. doi: 10.1136/oem.47.7.454. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Lohman P. H., Morolli B., Darroudi F., Natarajan A. T., Gossen J. A., Venema J., Mullenders L. H., Vogel E. W., Vrieling H., van Zeeland A. A. Contributions from molecular/biochemical approaches in epidemiology to cancer risk assessment and prevention. Environ Health Perspect. 1992 Nov;98:155–165. doi: 10.1289/ehp.9298155. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Lu L. J., Anderson L. M., Jones A. B., Moskal T. J., Salazar J. J., Hokanson J. A., Rice J. M. Persistence, gestation stage-dependent formation and interrelationship of benzo[a]pyrene-induced DNA adducts in mothers, placentae and fetuses of Erythrocebus patas monkeys. Carcinogenesis. 1993 Sep;14(9):1805–1813. doi: 10.1093/carcin/14.9.1805. [DOI] [PubMed] [Google Scholar]
  18. Newman M. J., Light B. A., Weston A., Tollurud D., Clark J. L., Mann D. L., Blackmon J. P., Harris C. C. Detection and characterization of human serum antibodies to polycyclic aromatic hydrocarbon diol-epoxide DNA adducts. J Clin Invest. 1988 Jul;82(1):145–153. doi: 10.1172/JCI113563. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Ovrebø S., Haugen A., Fjeldstad P. E., Hemminki K., Szyfter K. Biological monitoring of exposure to polycyclic aromatic hydrocarbon in an electrode paste plant. J Occup Med. 1994 Mar;36(3):303–310. doi: 10.1097/00043764-199403000-00007. [DOI] [PubMed] [Google Scholar]
  20. Ovrebø S., Haugen A., Phillips D. H., Hewer A. Detection of polycyclic aromatic hydrocarbon-DNA adducts in white blood cells from coke oven workers: correlation with job categories. Cancer Res. 1992 Mar 15;52(6):1510–1514. [PubMed] [Google Scholar]
  21. Sandven P., Eduard W. Detection and quantitation of antibodies against Rhizopus by enzyme-linked immunosorbent assay. APMIS. 1992 Nov;100(11):981–987. doi: 10.1111/j.1699-0463.1992.tb04029.x. [DOI] [PubMed] [Google Scholar]
  22. Santella R. M., Hemminki K., Tang D. L., Paik M., Ottman R., Young T. L., Savela K., Vodickova L., Dickey C., Whyatt R. Polycyclic aromatic hydrocarbon-DNA adducts in white blood cells and urinary 1-hydroxypyrene in foundry workers. Cancer Epidemiol Biomarkers Prev. 1993 Jan-Feb;2(1):59–62. [PubMed] [Google Scholar]
  23. Santella R. M., Perera F. P., Young T. L., Zhang Y. J., Chiamprasert S., Tang D., Wang L. W., Beachman A., Lin J. H., DeLeo V. A. Polycyclic aromatic hydrocarbon-DNA and protein adducts in coal tar treated patients and controls and their relationship to glutathione S-transferase genotype. Mutat Res. 1995 Apr;334(2):117–124. doi: 10.1016/0165-1161(95)90001-2. [DOI] [PubMed] [Google Scholar]
  24. Strickland P. T., Routledge M. N., Dipple A. Methodologies for measuring carcinogen adducts in humans. Cancer Epidemiol Biomarkers Prev. 1993 Nov-Dec;2(6):607–619. [PubMed] [Google Scholar]
  25. Tates A. D., Grummt T., Törnqvist M., Farmer P. B., van Dam F. J., van Mossel H., Schoemaker H. M., Osterman-Golkar S., Uebel C., Tang Y. S. Biological and chemical monitoring of occupational exposure to ethylene oxide. Mutat Res. 1991 Sep-Oct;250(1-2):483–497. doi: 10.1016/0027-5107(91)90205-3. [DOI] [PubMed] [Google Scholar]
  26. Törnqvist M., Osterman-Golkar S., Kautiainen A., Jensen S., Farmer P. B., Ehrenberg L. Tissue doses of ethylene oxide in cigarette smokers determined from adduct levels in hemoglobin. Carcinogenesis. 1986 Sep;7(9):1519–1521. doi: 10.1093/carcin/7.9.1519. [DOI] [PubMed] [Google Scholar]
  27. Vanrooij J. G., Bodelier-Bade M. M., De Looff A. J., Dijkmans A. P., Jongeneelen F. J. Dermal exposure to polycyclic aromatic hydrocarbons among primary aluminium workers. Med Lav. 1992 Sep-Oct;83(5):519–529. [PubMed] [Google Scholar]
  28. Vähäkangas K., Pyy L., Yrjänheikki E. Assessment of PAH-exposure among coke oven workers. Pharmacogenetics. 1992 Dec;2(6):304–308. [PubMed] [Google Scholar]
  29. Weliky N., Heiner D. C. A common pathway for chemical-induced tissue injury and immune responses leading to hypersensitivity and/or carcinogenesis. Med Hypotheses. 1985 Jan;16(1):69–91. doi: 10.1016/0306-9877(85)90041-6. [DOI] [PubMed] [Google Scholar]
  30. dell'Omo M., Lauwerys R. R. Adducts to macromolecules in the biological monitoring of workers exposed to polycyclic aromatic hydrocarbons. Crit Rev Toxicol. 1993;23(2):111–126. doi: 10.3109/10408449309117113. [DOI] [PubMed] [Google Scholar]

Articles from Occupational and Environmental Medicine are provided here courtesy of BMJ Publishing Group

RESOURCES