Cadmium-induced adaptive response in cells of Chinese hamster ovary cell lines with varying DNA repair capacity

Radiation Research

Volumn 171, Issue 4, 2009, Pages 446-453

  Pan, Yan ^a   Yuan, Dexiao ^a   Zhang, Junxiang ^a   Xu, Ping ^a   Chen, Honghong ^a   Shao, Chunlin ^a  

^a FUDAN UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

2 MORPHOLINO 6 (1 THIANTHRENYL) 4 PYRANONE; CADMIUM; PHOSPHATIDYLINOSITOL 3 KINASE; WORTMANNIN; 2 MORPHOLIN 4 YL 6 THIANTHREN 1 YL PYRAN 4 ONE; 2-MORPHOLIN-4-YL-6-THIANTHREN-1-YL-PYRAN-4-ONE; ANDROSTANE DERIVATIVE; ATM PROTEIN; CELL CYCLE PROTEIN; DNA BINDING PROTEIN; ENZYME INHIBITOR; MORPHOLINE DERIVATIVE; PROTEIN SERINE THREONINE KINASE; PYRONE DERIVATIVE; TUMOR SUPPRESSOR PROTEIN;

ADAPTATION; ANIMAL CELL; ARTICLE; CHO CELL; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; DNA DAMAGE; DNA REPAIR; DOUBLE STRANDED DNA BREAK; EXCISION REPAIR; FEMALE; IONIZING RADIATION; MOLECULAR MECHANICS; NONHUMAN; PRIORITY JOURNAL; RADIATION DOSE; SINGLE STRANDED DNA BREAK; ANIMAL; CRICETULUS; HAMSTER; METABOLISM; MICRONUCLEUS TEST; TUMOR CELL LINE;

ATAXIA TELANGIECTASIA; CRICETULUS GRISEUS;

1-PHOSPHATIDYLINOSITOL 3-KINASE; ANDROSTADIENES; ANIMALS; CADMIUM; CELL CYCLE PROTEINS; CELL LINE, TUMOR; CHO CELLS; CRICETINAE; CRICETULUS; DNA BREAKS, DOUBLE-STRANDED; DNA DAMAGE; DNA REPAIR; DNA-BINDING PROTEINS; ENZYME INHIBITORS; MICRONUCLEUS TESTS; MORPHOLINES; PROTEIN-SERINE-THREONINE KINASES; PYRONES; TUMOR SUPPRESSOR PROTEINS;

EID: 66149097832     PISSN: 00337587     EISSN: None     Source Type: Journal    
DOI: 10.1667/RR1491.1     Document Type: Article

References (60)

1. IARC, Beryllium, cadmium, mercury, and exposures in the glass manufacturing industry. Working Group views and expert opinions, Lyon, 9-16 February 1993. IARC Monogr. Eval. Carcinog. Risks Hum 58, 1-415 (1993).
2. M. Waisberg, P. Joseph, B. Hale and D. Beyersmann, Molecular and cellular mechanisms of cadmium carcinogenesis. Toxicology 192, 95-117 (2003).
3. G. Bertin and D. Averbeck, Cadmium: cellular effects, modifications of biomolecules, modulation of DNA repair and genotoxic consequences (a review). Biochimie 88, 1549-1559 (2006).
4. D. Beyersmann and S. Hechtenberg, Cadmium, gene regulation, and cellular signalling in mammalian cells. Toxicol. Appl. Pharmacol. 144, 247-261 (1997).
5. M. Deganuto, M. G. Pittis, A. Pines, S. Dominissini, M. R. Kelley, R. Garcia, F. Quadrifoglio, B. Bembi and G. Tell, Altered intracellular redox status in Gaucher disease fibroblasts and impairment of adaptive response against oxidative stress. J. Cell Physiol. 212, 223-235 (2007).
6. T. Miyahara, T. Katoh, M. Watanabe, Y. Mikami, S. Uchida, M. Hosoe, T. Sakuma, N. Nemoto, K. Takayama and T. Komurasaki, Involvement of mitogen-activated protein kinases and protein kinase C in cadmium-induced prostaglandin E2 production in primary mouse osteoblastic cells. Toxicology 200, 159-167 (2004).
7. D. Beyersmann, C. Block and A. N. Malviya, Effects of cadmium on nuclear protein kinase C. Environ. Health Perspect. 102 (Suppl. 3), 177-180 (1994).
8. S. Tapio and V. Jacob, Radioadaptive response revisited. Radiat. Environ. Biophys. 46, 1-12 (2007).
9. S. Wolff, Failla Memorial Lecture. Is radiation all bad? The search for adaptation. Radiat. Res. 131, 117-123 (1992).
10. H. Matsumoto, N. Hamada, A. Takahashi, Y. Kobayashi and T. Ohnishi, Vanguards of paradigm shift in radiation biology: radiation-induced adaptive and bystander responses. J. Radiat. Res. (Tokyo) 48, 97-106 (2007).
11. N. G. Oliveira, A. S. Rodrigues, T. Chaveca and J. Rueff, Induction of an adaptive response to quercetin, mitomycin C and hydrogen peroxide by low doses of quercetin in V79 Chinese hamster cells. Mutagenesis 12, 457-462 (1997).
12. T. Nikolova and E. Huttner, Adaptive and synergistic effects of a low-dose ENU pretreatment on the frequency of chromosomal aberrations induced by a challenge dose of ENU in human peripheral blood lymphocytes in vitro. Mutat. Res. 357, 131-141 (1996).
13. K. Schlade-Bartusiak, A. Stembalska-Kozlowska, M. Bernady, M. Kudyba and M. Sasiadek, Analysis of adaptive response to bleomycin and mitomycin C. Mutat. Res. 513, 75-81 (2002).
14. Z. H. Chen, Y. Yoshida, Y. Saito, N. Noguchi and E. Niki, Adaptive response induced by lipid peroxidation products in cell cultures. FEBS Lett. 580, 479-483 (2006).
15. L. Cai and M. G. Cherian, Adaptive response to ionizing radiation-induced chromosome aberrations in rabbit lymphocytes: effect of pre-exposure to zinc, and copper salts. Mutat. Res. 369, 233-241 (1996).
16. M. T. Leccia, M. J. Richard, J. C. Beani, H. Faure, A. M. Monjo, J. Cadet, P. Amblard and A. Favier, Protective effect of selenium and zinc on UV-A damage in human skin fibroblasts. Photochem. Photobiol. 58, 548-553 (1993).
17. P. Banjerdkij, P. Vattanaviboon and S. Mongkolsuk, Cadmium-induced adaptive resistance and cross-resistance to zinc in Xanthomonas campestris. Curr. Microbiol. 47, 260-262 (2003).
18. P. Banjerdkij, P. Vattanaviboon and S. Mongkolsuk, Exposure to cadmium elevates expression of genes in the OxyR and OhrR regulons and induces cross-resistance to peroxide killing treatment in Xanthomonas campestris. Appl. Environ. Microbiol. 71, 1843-1849 (2005).
19. S. Hornhardt, M. Gomolka, L. Walsh and T. Jung, Comparative investigations of sodium arsenite, arsenic trioxide and cadmium sulphate in combination with gamma-radiation on apoptosis, micronuclei induction and DNA damage in a human lymphoblastoid cell line. Mutat. Res. 600, 165-176 (2006).
20. M. Hartmann and A. Hartwig, Disturbance of DNA damage recognition after UV-irradiation by nickel(II) and cadmium(II) in mammalian cells. Carcinogenesis 19, 617-621 (1998).
21. M. J. Renan and P. I. Dowman, Increased radioresistance of tumor cells exposed to metallothionein-inducing agents. Radiat. Res. 120, 442-455 (1989).
22. O. A. Smoryzanova, B. I. Synzynys, I. A. Danilin and O. A. Baranova, Metallothionein content in tissue and neoplasms of mice under cadmium chloride administration and gamma irradiation. Increased radioresistance in mice with elevated level of metallothionein. Radiat. Biol. Radioecol. 44, 179-182 (2004).
23. K. Hanada, R. W. Gange, E. Siebert and T. Hasan, Protective effects of cadmium chloride against UVB injury in mouse skin and in cultured human cells: a possible role of cadmium-induced metallothionein. Photodermatol. Photoimmunol. Photomed. 8, 111-115 (1991).
24. M. Hayashi, A. Kawana, D. Endoh and T. Okui, Wortmannin, a radiation sensitizer, enhances the radiosensitivity of WKAH rat cells but not that of LEC rat cells. J. Vet. Med. Sci. 62, 191-194 (2000).
25. 1/S checkpoints in normal human fibroblasts. Br. J. Cancer 81, 959-965 (1999).
26. B. D. Price and M. B. Youmell, The phosphatidylinositol 3-kinase inhibitor wortmannin sensitizes murine fibroblasts and human tumor cells to radiation and blocks induction of p53 following DNA damage. Cancer Res. 56, 246-250 (1996).
27. I. Hickson, Y. Zhao, C. J. Richardson, S. J. Green, N. M. Martin, A. I. Orr, P. M. Reaper, S. P. Jackson, N. J. Curtin and G. C. Smith, Identification and characterization of a novel and specific inhibitor of the ataxia-telangiectasia mutated kinase ATM. Cancer Res. 64, 9152-9159 (2004).
28. L. Cai, S. Iskander, M. G. Cherian and R. R. Hammond, Zinc- or cadmium-pre-induced metallothionein protects human central nervous system cells and astrocytes from radiation-induced apoptosis. Toxicol. Lett. 146, 217-226 (2004).
29. H. Yamada and S. Koizumi, Lymphocyte metallothionein-mRNA as a sensitive biomarker of cadmium exposure. Ind. Health 39, 29-32 (2001).
30. D. K. Kim, E. S. Cho, J. K. Seong and H. D. Um, Adaptive concentrations of hydrogen peroxide suppress cell death by blocking the activation of SAPK/JNK pathway. J. Cell Sci. 114, 4329-4334 (2001).
31. S. H. Park, S. J. Lee, H. Y. Chung, T. H. Kim, C. K. Cho, S. Y. Yoo and Y. S. Lee, Inducible heat-shock protein 70 is involved in the radioadaptive response. Radiat. Res. 153, 318-326 (2000).
32. C. M. Kang, K. P. Park, C. K. Cho, J. S. Seo, W. Y. Park, S. J. Lee and Y. S. Lee, Hspa4 (HSP70) is involved in the radioadaptive response: results from mouse splenocytes. Radiat. Res. 157, 650-655 (2002).
33. K. Okaichi, K. Suzuki, N. Morita, M. Ikeda, H. Takahashi, N. Matsuda, M. Watanabe and Y. Okumura, Low dose of wortmannin reduces radiosensitivity of human glioblastoma cells through the p53 pathway. Oncol. Rep. 9, 859-862 (2002).
34. S. Khandelwal, S. J. Flora and S. K. Tandon, Possible role of nickel induced metallothionein (MT) in protection against cadmium nephrotoxicity. Z. Gesamte Hyg. 31, 400-403 (1985).
35. M. Viau, J. Gastaldo, Z. Bencokova, A. Joubert and N. Foray, Cadmium inhibits non-homologous end-joining and over-activates the MRE11-dependent repair pathway. Mutat. Res. 654, 13-21 (2008).
36. E. Sonoda, H. Hochegger, A. Saberi, Y. Taniguchi and S. Takeda, Differential usage of non-homologous end-joining and homologous recombination in double strand break repair. DNA Repair (Amst.) 5, 1021-1029 (2006).
37. T. Ikushima, H. Aritomi and J. Morisita, Radioadaptive response: efficient repair of radiation-induced DNA damage in adapted cells. Mutat. Res. 358, 193-198 (1996).
38. S. G. Chankova, E. Dimova, M. Dimitrova and P. E. Bryant, Induction of DNA double-strand breaks by zeocin in Chlamydomonas reinhardtii and the role of increased DNA double-strand breaks rejoining in the formation of an adaptive response. Radiat. Environ. Biophys. 46, 409-416 (2007).
39. S. G. Chankova and P. E. Bryant, Acceleration of DNA-double strand rejoining during the adaptive response of Chlamydomonas reinhardtii. Radiat. Biol. Radioecol. 42, 600-603 (2002).
40. E. Cappelli, R. Taylor, M. Cevasco, A. Abbondandolo, K. Caldecott and G. Frosina, Involvement of XRCC1 and DNA ligase III gene products in DNA base excision repair. J. Biol. Chem. 272, 23970-23975 (1997).
41. M. A. Coleman, E. Yin, L. E. Peterson, D. Nelson, K. Sorensen, J. D. Tucker and A. J. Wyrobek, Low-dose irradiation alters the transcript profiles of human lymphoblastoid cells including genes associated with cytogenetic radioadaptive response. Radiat. Res. 164, 369-382 (2005).
42. K. Hafer, K. K. Iwamoto, Z. Scuric and R. H. Schiestl, Adaptive response to gamma radiation in Mammalian cells proficient and deficient in components of nucleotide excision repair. Radiat. Res. 168, 168-174 (2007).
43. S. Wolff, The adaptive response in radiobiology: evolving insights and implications. Environ. Health Perspect. 106 (Suppl. 1), 277-283 (1998).
44. J. T. Heale, A. R. Ball, Jr., J. A. Schmiesing, J. S. Kim, X. Kong, S. Zhou, D. F. Hudson, W. C. Earnshaw and K. Yokomori, Condensin I interacts with the PARP-1-XRCC1 complex and functions in DNA single-strand break repair. Mol. Cell 21, 837-848 (2006).
45. S. F. El-Khamisy, M. Masutani, H. Suzuki and K. W. Caldecott, A requirement for PARP-1 for the assembly or stability of XRCC1 nuclear foci at sites of oxidative DNA damage. Nucleic Acids Res. 31, 5526-5533 (2003).
46. P. K. Zhou and O. Rigaud, Down-regulation of the human CDC16 gene after exposure to ionizing radiation: a possible role in the radioadaptive response. Radiat. Res. 155, 43-49 (2001).
47. B. A. Ulsh, S. M. Miller, F. F. Mallory, R. E. Mitchel, D. P. Morrison and D. R. Boreham, Cytogenetic dose-response and adaptive response in cells of ungulate species exposed to ionizing radiation. J. Environ. Radioact. 74, 73-81 (2004).
48. T. K. Day, G. Zeng, A. M. Hooker, M. Bhat, B. R. Scott, D. R. Turner and P. J. Sykes, Extremely low priming doses of X radiation induce an adaptive response for chromosomal inversions in pKZ1 mouse prostate. Radiat. Res. 166, 757-766 (2006).
49. T. K. Day, G. Zeng, A. M. Hooker, M. Bhat, B. R. Scott, D. R. Turner and P. J. Sykes, Adaptive response for chromosomal inversions in pKZ1 mouse prostate induced by low doses of X radiation delivered after a high dose. Radiat. Res. 167, 682-692 (2007).
50. L. M. Stoilov, L. H. Mullenders, F. Darroudi and A. T. Natarajan, Adaptive response to DNA and chromosomal damage induced by X-rays in human blood lymphocytes. Mutagenesis 22, 117-122 (2007).
51. E. Odegaard, C. R. Yang and D. A. Boothman, DNA-dependent protein kinase does not play a role in adaptive survival responses to ionizing radiation. Environ. Health Perspect. 106 (Suppl. 1), 301-305 (1998).
52. M. S. Sasaki, Y. Ejima, A. Tachibana, T. Yamada, K. Ishizaki, T. Shimizu and T. Nomura, DNA damage response pathway in radioadaptive response. Mutat. Res. 504, 101-118 (2002).
53. Y. Miura, K. Abe, S. Urano, T. Furuse, Y. Noda, K. Tatsumi and S. Suzuki, Adaptive response and the influence of ageing: effects of low-dose irradiation on cell growth of cultured glial cells. Int. J. Radiat. Biol. 78, 913-921 (2002).
54. Y. Miura, Oxidative stress, radiation-adaptive responses, and aging. J. Radiat. Res. (Tokyo) 45, 357-372 (2004).
55. J. Seong, C. O. Suh and G. E. Kim, Adaptive response to ionizing radiation induced by low doses of gamma rays in human cell lines. Int. J. Radiat. Oncol. Biol. Phys. 33, 869-874 (1995).
56. M. O'Driscoll and P. A. Jeggo, The role of double-strand break repair - insights from human genetics. Nat. Rev. Genet. 7, 45-54 (2006).
57. M. H. Son, K. W. Kang, C. H. Lee and S. G. Kim, Potentiation of cadmium-induced cytotoxicity by sulfur amino acid deprivation through activation of extracellular signal-regulated kinase1/2 (ERK1/2) in conjunction with p38 kinase or c-jun N-terminal kinase (JNK). Complete inhibition of the potentiated toxicity by U0126 an ERK1/2 and p38 kinase inhibitor. Biochem. Pharmacol. 62, 1379-1390 (2001).
58. K. Ito, A. Hirao, F. Arai, S. Matsuoka, K. Takubo, I. Hamaguchi, K. Nomiyama, K. Hosokawa, K. Sakurada and T. Suda, Regulation of oxidative stress by ATM is required for self-renewal of haematopoietic stem cells. Nature 431, 997-1002 (2004).
59. R. Brem, M. Fernet, B. Chapot and J. Hall, The methyl methanesulfonate induced S-phase delay in XRCC1-deficient cells requires ATM and ATR. DNA Repair (Amst.) 7, 849-857 (2008).
60. R. Aguilar-Quesada, J. A. Munoz-Gamez, D. Martin-Oliva, A. Peralta, M. T. Valenzuela, R. Martinez-Romero, R. Quiles-Perez, J. Menissier-de Murcia, G. de Murcia and F. J. Oliver, Interaction between ATM and PARP-1 in response to DNA damage and sensitization of ATM deficient cells through PARP inhibition. BMC Mol. Biol. 8, 29 (2007).