Genomic instability and catalase gene amplification induced by chronic exposure to oxidative stress

Cancer Research

Volumn 58, Issue 17, 1998, Pages 3986-3992

  Hunt, Clayton R ^a   Sim, Julia E ^a   Sullivan, Shannon J ^a   Featherstone, Terence ^a   Golden, Wendy ^b   Von Kapp Herr, Chris ^b   Hock, Randy A ^c   Gomez, R Ariel ^b   Parsian, Azemat J ^a   Spitz, Douglas R ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF VIRGINIA HEALTH SYSTEM   (United States)

^c INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CATALASE; HYDROGEN PEROXIDE; SUPEROXIDE;

ARTICLE; CONTROLLED STUDY; ENZYME INDUCTION; FIBROBLAST; GENE AMPLIFICATION; GENE MUTATION; HUMAN; HUMAN CELL; LONG TERM EXPOSURE; OXIDATIVE STRESS; PHENOTYPE; PRIORITY JOURNAL;

ADENINE PHOSPHORIBOSYLTRANSFERASE; ANIMALS; CATALASE; CELL LINE; GENE AMPLIFICATION; HUMANS; IN SITU HYBRIDIZATION; OXIDATIVE STRESS; RABBITS;

EID: 0032170014     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (47)

1. Sies, H. Oxidative stress: from basic research to clinical application. Am. J. Med., 91 (Suppl. 3C): 31S-38S, 1991.
2. Monteiro, H. P., and Stern, A. Redox modulation of tyrosine phosphorylation-dependent signal transduction pathways. Free Radic. Biol. Med., 21: 323-333, 1996.
3. 2. J. Biol. Chem., 271: 4138-4142, 1996.
4. Sun, Y., and Oberley, L. W. Redox regulation of transcriptional activators. Free Radic. Biol. Med., 21: 335-348, 1996.
5. Demple, B. Regulation of bacterial oxidative stress genes. Annu. Rev. Genet., 25: 315-337, 1991.
6. Budroe, J. D., Umemura, T., Angeloff, K., and Williams, G. M. Dose-response relationships of hepatic acyl-CoA oxidase and catalase activity and liver mitogenesis induced by the peroxisome proliferator ciprofibrate in C57BL/6N and BALB/c mice. Toxicol. Appl. Pharmacol., 113: 192-198, 1992.
7. Ames, B. N. Dietary carcinogens and anticarcinogens: oxygen radicals and degenerative diseases. Science (Washington DC), 221: 1256-1262, 1983.
8. Cerutti, P. A. Prooxidant states and tumor promotion. Science (Washington DC), 227: 375-381, 1985.
9. Cerutti, P., Larsson, R., Krupitza, G., Muehlematter, D., Crawford, D., and Amstad, P. Pathophysiological mechanisms of active oxygen. Mutat. Res., 214: 81-88, 1989.
10. Shay, J. W., and Werbin, H. Are mitochondrial DNA mutations involved in the carcinogenic process? Mutat. Res., 186: 149-160, 1987.
11. Moraes, E. C., Keyse, S. M., and Tyrrell, R. M. Mutagenesis by hydrogen peroxide treatment of mammalian cells: a molecular analysis. Carcinogenesis (Lond.), 11: 283-293, 1990.
12. 2-resistant Chinese hamster fibroblast cell lines. Arch. Biochem. Biophys., 279: 249-260, 1990.
13. 2-resistant fibroblasts. Arch. Biochem. Biophys., 292: 221-227, 1992.
14. 2-mediated injury. Am. J. Physiol. (Lung Cell. Mol. Physiol.), 262: L748-L756, 1992.
15. Spitz, D. R., Mackey, M. A., Li, G. C., Elwell, J. H., McCormick, M. L., and Oberley, L. W. Relationship between changes in ploidy and stable cellular resistance to hydrogen peroxide. J. Cell. Physiol., 139: 592-598, 1989.
16. 2 by catalase. J. Biol. Chem., 195: 133-140, 1952.
17. Aebi, H. Catalase in vitro. Methods Enzymol., 105: 121-126, 1984.
18. Lowry, O. H., Rosebrough, N. J., Farr, A. L., and Randall, R. J. Protein measurement with the folin phenol reagent. J. Biol. Chem., 193: 265-275, 1951.
19. Quan, F., Korneluk, R. G., Tropak, M. B., and Gravel, R. A. Isolation and characterization of the human catalase gene. Nucleic Acids Res., 14: 5321-5335, 1986.
20. Korneluk, R. G., Quan, F., Lewis, W. H., Guise, K. S., Willard, H. F., Holmes, M. T., and Gravel, R. A. Isolation of human fibroblast catalase cDNA clones. J. Biol. Chem., 259: 13819-13823, 1984.
21. Adair, G. M., Nairn, R. S., Wilson, J. H., Seidman, M. M., Brotherman, K. A., MacKinnon, C., and Scheerer, J. B. Targeted homologous recombination at the endogenous adenine phosphoribosyltransferase locus in Chinese hamster cells. Proc. Natl. Acad. Sci. USA, 86: 4574-4578, 1989.
22. Zabel, B. U., Naylor, S. L., Sakaguchi, A. Y., Bell, G. I., and Shows, T. B. High resolution chromosomal localization of human genes for amylase, propiomelanocortin, somatostatin, and a DNA fragment (D351) by in situ hybridization. Proc. Natl. Acad. Sci. USA, 80: 6932-6936, 1983.
23. Adair, G. M., Stallings, R. L., and Siciliano, M. J. Chromosomal rearrangements and gene expression in CHO cells: mapping of alleles for eight enzyme loci on CHO chromosomes Z3, Z4, Z5, and Z7. Somat. Cell Mol. Genet., 10: 283-95, 1984.
24. Chen, M-S., Featherstone, T., and Laszlo, A. Amplification and altered expression of the hsc70/U14 snoRNA gene in a heat-resistant Chinese hamster cell line. Cell Stress Chaperones, 1: 47-61, 1996.
25. Lichter, P., and Cremer, T. Chromosome analysis by non-isotopic in situ hybridization. In: D. E. Rooney and B. H Czepulkowski (eds.), Human Cytogenetics: A Practical Approach, pp. 157-191, New York: IRL Press, 1992.
26. Adair, G. M., Nairn, R. S., Brotherman, K. A., and Siciliano, M. J. Spontaneous CHO APRT heterozygotes reflect high-frequency allele-specific deletion of the chromosome Z4 APRT gene. Somat. Cell Mol. Genet., 15: 535-544, 1989.
27. Coquelle, A., Pipiras, E., Toledo, F., Buttin, G., and Debatisse, M. Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons. Cell, 89: 215-225, 1997.
28. Kuo, M. T., Vyas, R. C., Jiang, L. X., and Hittelman, W. Chromosome breakage at a major fragile site associated with P-glycoprotein gene amplification in multidrug-resistant CHO cells. Mol. Cell. Biol., 14: 5202-5211, 1994.
29. Yu, S., Magelsdorf, M., Hewett, D., Hobson, L., Baker, E. Eyre, H. J., Lapsys, N., Le Paslier, D., Doggett, N. A., Sutherland, G. R., and Richards, R. I. Human fragile site FRA16B is an amplified AT-rich minisatellite repeat. Cell, 88: 367-374, 1997.
30. Gille, J. P., Mullaart, E., Vijg, J., Leyva, A. L., Arwert, F., and Joenje, H. Chromosomal instability in an oxygen-tolerant variant of Chinese hamster ovary cells. Mutat. Res., 219: 17-28, 1989.
31. Dallapiccola, B., Porfirio, B., Mokini, V., Alimena, G., Isacchi, G., and Gandini, E. Effects of oxidants and antioxidants on chromosomal breakage in Fanconi anemia lymphocytes. Hum. Genet., 69: 62-65, 1985.
32. Cooper, G. M. Oncogenes, pp. 100-102. Sudbury, MA: Jones and Bartlett Publishers, 1995.
33. Sognier, M. A., Zhang, Y., Eberle, R. L., and Belli, J. A. Characterization of Adriamycin-resistant Chinese hamster cell lines. Biochem. Pharmacol., 44: 1859-1868, 1992.
34. Vatteroni, L., Piras, A., Moretti, A., and Rainaldi, G. Gene amplification and gene deletion are induced at different rates in V79/AP4 Chinese hamster cells. Mutagenesis, 8: 411-415, 1993.
35. Rossman, T. G., and Wolosin, D. Differential susceptibility to carcinogen-induced amplification of SV40 and dhfr sequences in SV40-transformed human keratinocytes. Mol. Carcinog., 6: 203-213, 1992.
36. Quinto, H., Scala, G., Mallardo, M., Arcucci, A., Ruocco, M. R., and De Lorenzo, F. Spontaneous and mutagen-mediated amplification of a neo gene integrated at different genomic sites in rat 2 fibroblasts. Carcinogenesis (Lond.), 13: 439-445, 1992.
37. Lewis, A. D., Hickson, I. D., Robson, C. N., Harris, A. L., Hayes, J. D., Griffiths, S. A., Manson, M. M., Hall, A. E., Moss, J. E., and Wolf, C. R. Amplification and increased expression of a class glutathione S-transferase-encoding genes associated with resistance to nitrogen mustards. Proc. Natl. Acad. Sci. USA, 85: 8511-8515, 1988.
38. Hahn, P., Nevaldine, B., and Morgan W. F. X-ray induction of methotrexate resistance due to dhfr gene amplification. Somat. Cell Mol. Genet., 16: 413-423, 1990.
39. Lucke-Huhle, C., and Herrlich, P. Retinoic acid-induced differentiation prevents gene amplification in teratocarcinoma stem cells. Int. J. Cancer, 47: 461-465, 1991.
40. 2-resistant fibroblasts. J. Cell. Physiol., 15: 72-79, 1993.
41. Lin, F., Jackson, V. E., and Girotti, A. W. Amplification and hyperexpression of the catalase gene in selenoperoxidase-deficient leukemia cells. Arch. Biochem. Biophys., 317: 7-18, 1995.
42. Yamada, M., Hashinaka, K., Inazawa, J., and Abe, T. Expression of catalase and myeloperoxidase genes in hydrogen peroxide-resistant HL-60 cells. DNA Cell Biol., 10: 735-742, 1991.
43. Anderson, M. W., Reynolds, S. H., You, M., and Maronpot, R. M. Role of protooncogene activation in carcinogencsis. Environ. Health Perspect., 98: 13-24, 1992.
44. Szatrowski, T. P., and Nathan, C. F. Production of large amounts of hydrogen peroxide by human tumor cells. Cancer Res., 51: 794-798, 1991.
45. Oberley, L. W., Oberley, T. D., and Buettner, G. R. Cell division in normal and transformed cells: the possible role of superoxide and hydrogen peroxide. Med. Hypotheses, 7: 21-42, 1981.
46. McKenna, W. G., Weiss, M. C., Endlich, B., Ling, C. C., Bakanauskas, V. J., Kelsten, M. L., and Muschel, R. J. Synergistic effect of the v-myc oncogene with H-rav on radioresistance. Cancer Res., 50: 97-102, 1990.
47. Biaglow, J. E., Cerniglia, G., Tuttle, S., Bakanauskas, V., Stevens, C., and McKenna, G. Effect of oncogene transformation of rat embryo cells on cellular oxygen consumption and glycolysis. Biochem. Biophys. Res. Commun., 235: 739-742, 1997.