Enhancement of myeloid cell growth by benzene metabolites via the production of active oxygen species

Free Radical Research

Volumn 30, Issue 2, 1999, Pages 93-103

  Wiemels, Joseph ^a,b   Smith, Martyn T ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b INSTITUTE OF CANCER RESEARCH   (United Kingdom)

Author keywords

Active oxygen; Benzene; Benzoquinone; Cell cycle; Cell growth; Hydroquinone; Leukemia

Indexed keywords

BENZENE DERIVATIVE; BENZOQUINONE; CATALASE; FREE RADICAL; GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR; HYDROQUINONE; THYMIDINE; TRITIUM; XANTHINE; XANTHINE OXIDASE;

ARTICLE; BONE MARROW CELL; CELL CLONING; CELL CYCLE PHASE; CELL DIFFERENTIATION; CELL GROWTH; COLONY FORMATION; CONTROLLED STUDY; GRANULOCYTE; HEMATOPOIESIS; HUMAN; HUMAN CELL; INHIBITION KINETICS; LEUKEMIA; METABOLITE; MITOGENESIS; STEM CELL;

TRITIUM;

EID: 0033060036     PISSN: 10715762     EISSN: None     Source Type: Journal    
DOI: 10.1080/10715769900300101     Document Type: Article

References (42)

1. R. Snyder and C.C. Hedli (1996). An overview of benzene metabolism. Environmental Health Perspectives, 104, 1165-71.
2. M.T. Smith (1996). The mechanism of benzene-induced leukemia: a hypothesis and speculations on the causes of leukemia. Environmental Health Perspectives, 104, 1219-25.
3. R. Henschler, H.R. Glatt and C.M. Heyworth (1996). Hydroquinone stimulates granulocyte-macrophage progenitor cells in vitro and in vivo. Environmental Health Perspectives, 104, 1271-4.
4. C.C. Hedli, N.R. Rao, K.R. Reuhl, C.M. Witmer and R. Snyder (1996). Effects of benzene metabolite treatment on granulocytic differentiation and DNA adduct formation in HL-60 cells. Archives of Toxicology, 70, 135-44.
5. B.A. Hazel and G.F. Kalf (1996). Induction of granulocytic differentiation in myeloblasts by hydroquinone, a metabolite of benzene, involves the leukotriene D4 receptor. Receptors and Signal Transduction, 6, 1-12.
6. B.A. Hazel, A. O'Conner, R. Nicelescu and G. Kalf (1995). Benzene and its metabolite hydroquinone induce granulocytic differentiation in myeloblasts by interacting with cellular signalling pathways activated by granulocyte colony-stimulating factor. Stem Cells, 13, 295-300.
7. G.F. Kalf and A. O'Conner (1993). The effects of benzene and hydroquinone on myeloid differentiation of HL-60 promyelocytic leukemia cells. Leukemia and Lymphoma, 11, 331-38.
8. R.D. Irons, W.S. Stillman, D.G. Calagiovanni and V.A. Henry (1992). Synergistic action of the benzene metabolite hydroquinone on myelopoietic stimulating activity of granulocyte/mecrophage colony-stimulating factor in vitro. Proceedings of the National Academy of Sciences USA, 89, 3691-5.
9. A.M. Dempster and C.A. Snyder (1991). Kinetics of granulocyte and erythroid progenitor cells are affected differently by short term, low level benzene exposure. Archives of Toxicology, 65, 556-65.
10. J.L. Moran, D. Siegel, X.-M. Sun and D. Ross (1996). Induction of Apoptosis by benzene metabolites in HL60 and CD34+ human bone marrow progenitor cells. Molecular Pharmacology, 50, 610-15.
11. Y. Hiraku and S. Kawanishi (1996). Oxidative damage and apoptosis induced by benzene metabolites. Cancer Research, 56, 5172-8.
12. B.A. Hazel, C. Baum and G.A. Kalf (1996). Hydroquinone, a bioreactive metabolite of benzene, inhibits apoptosis in mycloblasts. Stem Cells, 14, 730-42.
13. P. Kolachana, V.V. Subrahmanyam, K.B. Meyer, L. Zhang and M.T. Smith (1993). Benzene and its phenolic metabolites produce oxidative DNA damage in HL60 cells in vitro and in the bone marrow in vivo. Cancer Research, 53, 1023-6.
14. L. Zhang, M.T. Smith, B. Bandy, S.J. Tamaki (1994). Role of quinones, active oxygen species and metals in the genotoxicity of 1,2,4-benzenetriol, a metabolite of benzene. In Free Radicals in the Environment, Medicine, and Toxicology" (eds., H. Nohl, H. Esterbauer, and C. Rice-Evans), Richelieu Press, London, pp. 521-58.
15. D.A. Stoyanovsky, R. Goldman, H.G. Claycamp and V.E. Kagan (1995). Phenoxyl radical-induced thiol-dependent generation of reactive oxygen species: implications for benzene toxicity. Archives of Biochemistry and Biophysics, 317, 315-23.
16. V.V. Subrahmanyam, P. Kolachana and M.T. Smith (1991). Metabolism of hydroquinone by human myelopperoxidase: mechanisms of stimulation by other phenolic compounds. Archives of Biochemistry and Biophysics, 286, 76-84.
17. N.R. Rao and R. Snyder (1995). Oxidative modifications produced in HL-60 cells on exposure to benzene metabolites, Journal of Applied Toxicology, 15, 403-09.
18. L. Liu, Q. Zhang, J. Feng, L. Deng, N. Zeng, A. Yang and W. Zhang (1996). The study of DNA oxidative damage in benzene-exposed workers. Mutation Research, 370, 145-50.
19. G. Powis (1989). Free radical formation by antitumor quinones. Free Radical Biology and Medicine, 6, 63-101.
20. K. Dobo and D. Eastmond (1994). Role of oxygen radicals in the chromosomal loss and breakage induced by the quinone-forming compounds, hydroquinone and tertbutylhydroquinone. Environmental and Molecular Mutagenesis, 24, 293-300.
21. P. Cerutti (1985). Prooxidant states and tumor promotion. Science, 227, 375-81.
22. D. Muehlematter, R. Larsson and P. Cerutti (1988). Active oxygen induced DNA strand breakage and poly ADP-ribosylation in promotable and non-promotable JB6 mouse epidermal cells. Carcinogenesis, 9, 239-45.
23. G.A. Murrell, M.J.O. Francis and L. Bromley (1990). Modulation of fibroblast proliferation by oxygen free radicals. Biochemical Journal, 265, 659-65.
24. R.H. Burdon, D. Alliangana and V. Gill (1995). Hydrogen peroxide and the proliferation of BHK-21 cells. Free Radical Research, 23, 471-86.
25. R.H. Burdon (1995). Superoxide and hydrogen peroxide in relation to mammalian cell proliferation. Free Radical Biology and Medicine, 18, 775-94.
26. R.H. Burdon, D. Alliangana and V. Gill (1994). Endogenously generated active oxygen species and cellular glutathione levels in relation to BHK-21 cell proliferation. Free Radical Research, 21, 121-33.
27. H. Nakamura, K. Nakamura and J. Yodoi (1997). Redox regulation of cellular activation. Annual Review of Immunology, 15, 351-69.
28. D.W. Pyatt, W.S. Stillman and R.D. Irons (1996). Reactive oxygen species mediate the stem cell factor synergy with granulocyte/macrophage colony-stimulating factor in a subpopulation of primitive murine hematopoietic progenitor cells. Molecular Pharmacology, 49, 1097-103.
29. R.D. Irons and W.S. Stillman (1993). Cell proliferation and differentiation in chemical leukemogenesis. Stem Cells, 11, 235-42.
30. K. Irani, Y. Xia, J.L. Zweier, S.J. Sollet, C.J. Der, E.R. Fearon, M. Sundaresan, T. Finkel and P.J. Goldschmidt-Clermont (1997). Mitogenic signaling mediated by oxidants in Ras-transformed fibroblasts. Science, 275, 1649-52.
31. M. Shibanamu, T. Kuroki and K. Nose (1988). Induction of DNA replication and expression of proto-oncogene c-myc and c-fos in quiescent Balb/3T3 cells by xanthine/xanthine oxidase. Oncogene, 3, 17-21.
32. D.W. Kufe (1993). Reactive oxygen intermediates target CC(A/T)6GG sequences to mediate activation of the early growth response 1 transcription factor gene by ionizing radiation. Proceedings of the National Academy of Sciences USA, 90, 2419-2.
33. M. Los, W. Droge, K. Stricker, P.A. Baeurle and K. Schulze-Osthoff (1995). Hydrogen peroxide as an activator of T-lymphocyte functions. European Journal of Immunology, 25, 159-65.
34. V.V. Subrahmanyam, D. Ross, D.A. Eastmond and M.T. Smith (1991). Potential role of free radicals in benzene-induced myelotoxicity and leukemia. Free Radical Biology and Medicine, 11, 495-515.
35. G.M. Farris, S.N. Robinson, K.W. Gaido, B.A. Wong, V.A. Wong, W.P. Hahn and R.S. Shah (1997). Benzene-induced hematotoxicity and bone marrow compensation in B6C3FI mice. Fundamental and Applied Toxicology, 36, 119-29.
36. G.T. Williams, C.A. Smith, E. Spooncer, T.M. Dexter and D.R. Taylor (1990). Haematpoietic colony stimulating factors promote cell survival by preventing apoptosis. Nature, 343, 76-79.
37. W. Meikrantz and R. Schlegel (1995). Apoptosis and the cell cycle. Journal of Cellular Biochemistry, 58, 160-174.
38. C. Abate, L. Patel, F.J. Rauscher and T. Curran (1990). Redox regulation of Fos and Jun DNA-binding activity in vitro. Science, 249, 1157-61.
39. F. Cimino, F. Esposito, R. Ammendola and T. Russo (1997). Gene regulation by reactive oxygen species. Current Topics in Cell Regulation, 35, 123-48.
40. M.P. Boland, S.J. Foster and L.A. O'Neill (1997). Daunorubicin activates NFkappaB and induces kappaB-dependent gene expression in HL-60 promyelocytic and Jurkat T lymphoma cells. The Journal of Biological Chemistry, 272, 12952-60.
41. D.W. Pyatt, W.S. Stillman (1998). Hydroquinone, a reactive metabolite of benzene, inhibits NF-kappa B in primary human CD4+ T lymphocytes. Toxicology and Applied Pharmacology, 149, 178-84.
42. T.Y. Ho and G. Witz (1997). Increased gene expression in human promyeloid leukemia cells exposed to trans,transmuconaldehyde, a hematotoxic benzene metabolite. Carcinogenesis, 18, 739-44.