An association between oxidative stress and radiation-induced lymphomagenesis

Radiation Research

Volumn 161, Issue 6, 2004, Pages 642-647

  Suzuki, Gen ^a   Shimada, Yoshiya ^b   Hayashi, Tomonori ^a   Akashi, Makoto ^b   Hirama, Toshiyasu ^b   Kusunoki, Yoichiro ^a  

^a RADIATION EFFECTS RESEARCH FOUNDATION   (Japan)

^b NATIONAL INSTITUTE OF RADIOLOGICAL SCIENCES   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CD4 ANTIGEN; CD8 ANTIGEN; REACTIVE OXYGEN METABOLITE; RHODAMINE 123; T LYMPHOCYTE RECEPTOR;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; FEMALE; FLOW CYTOMETRY; GENE REARRANGEMENT; LYMPHOMA; MOUSE; NONHUMAN; OXIDATIVE STRESS; PATHOPHYSIOLOGY; PRECANCER; PRIORITY JOURNAL; RADIATION CARCINOGENESIS; RADIOBIOLOGY; T LYMPHOCYTE RECEPTOR GENE; THYMUS; ANIMAL; C57BL MOUSE; CELL CULTURE; COMPARATIVE STUDY; EVALUATION; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; RADIATION DOSE; RADIATION EXPOSURE; RADIATION INJURY; REFERENCE VALUE; STATISTICS; THYMOMA; WHOLE BODY RADIATION;

ANIMALS; FEMALE; GENE EXPRESSION REGULATION, NEOPLASTIC; LYMPHOMA; MICE; MICE, INBRED C57BL; NEOPLASMS, RADIATION-INDUCED; OXIDATIVE STRESS; RADIATION DOSAGE; RADIATION TOLERANCE; REACTIVE OXYGEN SPECIES; REFERENCE VALUES; STATISTICS; THYMUS NEOPLASMS; TUMOR CELLS, CULTURED; WHOLE-BODY IRRADIATION;

EID: 3042667650     PISSN: 00337587     EISSN: None     Source Type: Journal    
DOI: 10.1667/RR3188     Document Type: Article

References (25)

1. A. G. Knudson, Antioncogenes and human cancer. Proc. Natl. Acad. Sci. USA 90, 10914-10921 (1993).
2. A. L. Jackson and L. A. Loeb, The contribution of endogenous sources of DNA damage to the multiple mutations in cancer. Mutat. Res. 477, 7-21 (2001).
3. D. E. Thompson, K. Mabuchi, E. Ron, M. Soda, M. Tokunaga, S. Ochikubo, S. Sugimoto, T. Ikeda, M. Terasaki and S. Izumi, Cancer incidence in atomic bomb survivors. Part II: Solid tumors, 1958-1987. Radiat. Res. 137 (Suppl.), S17-S67 (1994).
4. J. S. Bedford and W. C. Dewey, Historical and current highlights in radiation biology: Has anything important been learned by irradiating cells? Radiat. Res. 158, 251-291 (2002).
5. M. A. Kadhim, D. A. Macdonald, D. T. Goodhead, S. A. Lorimore, S. J. Marsden and E. G. Wright, Transmission of chromosomal instability after plutonium alpha-particle irradiation. Nature 355, 738-740 (1992).
6. S. A. Lorimore, M. A. Kadhim, D. A. Pocock, D. Papworth, D. L. Stevens, D. T. Goodhead and E. G. Wright, Chromosomal instability in the descendants of unirradiated surviving cells after alpha-particle irradiation. Proc. Natl. Acad. Sci. USA 95, 5730-5733 (1998).
7. J. B. Little, H. Nagasawa, T. Pfenning and H. Vetrovs, Radiation-induced genomic instability: Delayed mutagenic and cytogenetic effects of X rays and alpha particles. Radiat. Res. 148, 299-307 (1997).
8. M. Shimizu, P. Gruz, H. Kamiya, S. R. Kim, F. M. Pisani, C. Masutani, Y. Kanke, H. Harashima and F. Hanaoka, Erroneous incorporation of oxidized DNA precursors by Y-family DNA polymerases. EMBO Rep. 4, 269-273 (2003).
9. W. Yang, Damage repair DNA polymerases Y. Curr. Opin. Struct. Biol. 13, 23-30 (2003).
10. S. M. Clutton, K. M. Townsend, C. Walker, J. D. Ansell and E. G. Wright, Radiation-induced genomic instability and persisting oxidative stress in primary bone marrow cultures. Carcinogenesis 17, 1633-1639 (1996).
11. J. L. Redpath and M. Gutierrez, Kinetics of induction of reactive oxygen species during the post-irradiation expression of neoplastic transformation in vitro. Int. J. Radiat. Biol. 77, 1081-1085 (2001).
12. R. E. Rugo, M. B. Secretan and R. H. Schiestl, X radiation causes a persistent induction of reactive oxygen species and a delayed reinduction of TP53 in normal human diploid fibroblasts. Radiat. Res. 158, 210-219 (2002).
13. M. Muto, E. Kubo and T. Sado, Development of prelymphoma cells committed to thymic lymphomas during radiation-induced thymic lymphomagenesis in B10 mice. Cancer Res. 47, 3469-3472 (1987).
14. H. Kawamoto, K. Ohmura, S. Fujimoto, M. Lu, T. Ikawa and Y. Katsura, Extensive proliferation of T cell lineage-restricted progenitors in the thymus: An essential process for clonal expression of diverse T cell receptor beta chains. Eur. J. Immunol. 33, 606-615 (2003).
15. M. J. Bevan, In thymic selection, peptide diversity gives and takes away. Immunity 7, 175-178 (1997).
16. G. Anderson, K. J. Hare and E. J. Jenkinson, Positive selection of thymocytes: The long and winding road. Immunol. Today 20, 463-468 (1999).
17. J. Kumagai, K. Masui, Y. Itagaki, M. Shiotani, S. Kodama, M. Watanabe and T. Miyazaki, Long-lived mutagenic radicals induced in mammalian cells by ionizing radiation are mainly localized to proteins. Radiat. Res. 160, 95-102 (2003).
18. J. K. Leach, G. Van Tuyle, P. S. Lin, R. Schmidt-Ullrich and R. B. Mikkelsen, Ionizing radiation-induced, mitochondria-dependent generation of reactive oxygen/nitrogen. Cancer Res. 61, 3894-3901 (2001).
19. K. Polyak, Y. Xia, J. L. Zweier, K. W. Kinzler and B. Vogelstein, A model for p53-induced apoptosis. Nature 389, 300-305 (1997).
20. G. Kroemer, N. Zamzami and S. A. Susin, Mitochondrial control of apoptosis. Immunol. Today 18, 44-51 (1997).
21. C. L. Limoli, E. Giedzinski, W. F. Morgan, S. G. Swarts, G. D. Jones and W. Hyun, Persistent oxidative stress in chromosomally unstable cells. Cancer Res. 63, 3107-3111 (2003).
22. S. DiMauro and E. A. Schon, Mitochondrial respiratory-chain diseases. N. Engl. J. Med. 348, 2656-2668 (2003).
23. I. N. Zelko, T. J. Mariani and R. J. Folz, Superoxide dismutase multigene family: A comparison of the CuZn-SOD (SOD1), Mn-SOD (SOD2), and EC-SOD (SOD3) gene structures, evolution, and expression. Free Radic. Biol. Med. 33, 337-349 (2002).
24. H. C. Lee and Y. H. Wei, Mitochondrial alterations, cellular response to oxidative stress and defective degradation of proteins in aging. Biogerontology 2, 231-244 (2001).
25. Y. H. Wei, C. F. Lee, H. C. Lee, Y. S. Ma, C. W. Wang, C. Y. Lu and C. Y. Pang, Increases of mitochondrial mass and mitochondrial genome in association with enhanced oxidative stress in human cells harboring 4,977 BP-deleted mitochondrial DNA. Ann. NY Acad. Sci. 928, 97-112 (2001).