Cadmium induced radioadaptive response via an ATM-independent H2S/cystathionine γ-lyase modulation

Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis

Volumn 707, Issue 1-2, 2011, Pages 67-73

  Pan, Yan ^a   Yuan, Dexiao ^a   Zhang, Jianghong ^a   Shao, Chunlin ^a  

^a FUDAN UNIVERSITY   (China)

Author keywords

Adaptive response; ATM; Cadmium; H2S; Irradiation

Indexed keywords

AMINOOXYACETIC ACID; ATM PROTEIN; CADMIUM; CYSTATHIONINE BETA SYNTHASE; CYSTATHIONINE GAMMA LYASE; HYDROGEN SULFIDE; PROPARGYLGLYCINE;

ADAPTATION; ARTICLE; CONCENTRATION RESPONSE; CONTROLLED STUDY; DOWN REGULATION; GAMMA IRRADIATION; HUMAN; HUMAN CELL; LIVER CELL; MICRONUCLEUS; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN PHOSPHORYLATION; TIME; UPREGULATION;

ADAPTATION, PHYSIOLOGICAL; CADMIUM; CELL CYCLE PROTEINS; CELL LINE; CYSTATHIONINE GAMMA-LYASE; DNA-BINDING PROTEINS; HUMANS; HYDROGEN SULFIDE; PROTEIN-SERINE-THREONINE KINASES; SIGNAL TRANSDUCTION; TUMOR SUPPRESSOR PROTEINS;

EID: 79251600081     PISSN: 00275107     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mrfmmm.2010.12.014     Document Type: Article

References (48)

1. Omata Y., Saito Y., Fujita K., Ogawa Y., Nishio K., Yoshida Y., Niki E. Induction of adaptive response and enhancement of PC12 cell tolerance by lipopolysaccharide primarily through the upregulation of glutathione S-transferase A3 via Nrf2 activation. Free Radic. Biol. Med. 2008, 45:1437-1445.
2. Chen Z.H., Yoshida Y., Saito Y., Sekine A., Noguchi N., Niki E. Induction of adaptive response and enhancement of PC12 cell tolerance by 7-hydroxycholesterol and 15-deoxy-delta(12, 14)-prostaglandin J2 through up-regulation of cellular glutathione via different mechanisms. J. Biol. Chem. 2006, 281:14440-14445.
3. Lanza V., Pretazzoli V., Olivieri G., Pascarella G., Panconesi A., Negri R. Transcriptional response of human umbilical vein endothelial cells to low doses of ionizing radiation. J. Radiat. Res. (Tokyo) 2005, 46:265-276.
4. Coleman M.A., Yin E., Peterson L.E., Nelson D., Sorensen K., Tucker J.D., Wyrobek A.J. Low-dose irradiation alters the transcript profiles of human lymphoblastoid cells including genes associated with cytogenetic radioadaptive response. Radiat. Res. 2005, 164:369-382.
5. Wolff S. Failla memorial lecture. Is radiation all bad? The search for adaptation. Radiat. Res. 1992, 131:117-123.
6. Ermakov A.V., Konkova M.S., Kostyuk S.V., Egolina N.A., Efremova L.V., Veiko N.N. Oxidative stress as a significant factor for development of an adaptive response in irradiated and nonirradiated human lymphocytes after inducing the bystander effect by low-dose X-radiation. Mutat. Res. 2009, 669:155-161.
7. Liu J., Qu W., Kadiiska M.B. Role of oxidative stress in cadmium toxicity and carcinogenesis. Toxicol. Appl. Pharmacol. 2009, 238:209-214.
8. Bertin G., Averbeck D. Cadmium: cellular effects, modifications of biomolecules, modulation of DNA repair and genotoxic consequences (a review). Biochimie 2006, 88:1549-1559.
9. Joseph P Mechanisms of cadmium carcinogenesis. Toxicol. Appl. Pharmacol. 2009, 238:272-279.
10. Viau M., Gastaldo J., Bencokova Z., Joubert A., Foray N. Cadmium inhibits non-homologous end-joining and over-activates the MRE11-dependent repair pathway. Mutat. Res. 2008, 654:13-21.
11. Hornhardt S., Gomolka M., Walsh L., Jung T. 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. 2006, 600:165-176.
12. Grygoryev D, Moskalenko O., Zimbrick J.D. Non-linear effects in the formation of DNA damage in medaka fish fibroblast cells caused by combined action of cadmium and ionizing radiation. Dose Resp. 2008, 6:283-298.
13. Michel C., Balla I. Interaction between radiation and cadmium or mercury in mouse embryos during organogenesis. Int. J. Radiat. Biol. Relat. Stud. Phys. Chem. Med. 1987, 51:1007-1019.
14. Renan M.J., Dowman P.I. Increased radioresistance of tumor cells exposed to metallothionein-inducing agents. Radiat. Res. 1989, 120:442-455.
15. Smoryzanova O.A., Synzynys B.I., Danilin I.A., Baranova O.A. 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. 2004, 44:179-182.
16. Hanada K., Gange R.W., Siebert E., Hasan T. 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. 1991, 8:111-115.
17. Wang R. Two's company, three's a crowd: can H2S be the third endogenous gaseous transmitter?. FASEB J. 2002, 16:1792-1798.
18. Yang G, Wu L., Jiang B., Yang W., Qi J., Cao K., Meng Q., Mustafa A.K., Mu W., Zhang S., Snyder S.H., Wang R. H2S as a physiologic vasorelaxant: hypertension in mice with deletion of cystathionine gamma-lyase. Science 2008, 322:587-590.
19. Zanardo R.C., Brancaleone V., Distrutti E., Fiorucci S., Cirino G., Wallace J.L. Hydrogen sulfide is an endogenous modulator of leukocyte-mediated inflammation. FASEB J. 2006, 20:2118-2120.
20. Abe K., Kimura H. The possible role of hydrogen sulfide as an endogenous neuromodulator. J. Neurosci. 1996, 16:1066-1071.
21. Kimura H. Hydrogen sulfide as a neuromodulator. Mol. Neurobiol. 2002, 26:13-19.
22. Hosoki R., Matsuki N., Kimura H. The possible role of hydrogen sulfide as an endogenous smooth muscle relaxant in synergy with nitric oxide. Biochem. Biophys. Res. Commun. 1997, 237:527-531.
23. Zhao W., Zhang J., Lu Y., Wang R. The vasorelaxant effect of H(2)S as a novel endogenous gaseous K(ATP) channel opener. EMBO J. 2001, 20:6008-6016.
24. Nagai Y., Tsugane M., Oka J., Kimura H. Hydrogen sulfide induces calcium waves in astrocytes. FASEB J. 2004, 18:557-559.
25. Baskar R., Li L., Moore P.K. Hydrogen sulfide-induces DNA damage and changes in apoptotic gene expression in human lung fibroblast cells. FASEB J. 2007, 21:247-255.
26. Pan Y., Yuan D., Zhang J., Xu P., Chen H., Shao C. Cadmium-induced adaptive response in cells of Chinese hamster ovary cell lines with varying DNA repair capacity. Radiat. Res. 2009, 171:446-453.
27. Kim D.K., Cho E.S., Seong J.K., Um H.D. Adaptive concentrations of hydrogen peroxide suppress cell death by blocking the activation of SAPK/JNK pathway. J. Cell Sci. 2001, 114:4329-4334.
28. Park S.H., Lee S.J., Chung H.Y., Kim T.H., Cho C.K., Yoo S.Y., Lee Y.S. Inducible heat-shock protein 70 is involved in the radioadaptive response. Radiat. Res. 2000, 153:318-326.
29. Kang C.M., Park K.P., Cho C.K., Seo J.S., Park W.Y., Lee S.J., Lee Y.S. Hspa4 (HSP70) is involved in the radioadaptive response: results from mouse splenocytes. Radiat. Res. 2002, 157:650-655.
30. Okaichi K., Suzuki K., Morita N., Ikeda M., Takahashi H., Matsuda N., Watanabe M., Okumura Y. Low dose of wortmannin reduces radiosensitivity of human glioblastoma cells through the p53 pathway. Oncol. Rep. 2002, 9:859-862.
31. Cai L., Iskander S., Cherian M.G., Hammond R.R. Zinc- or cadmium-pre-induced metallothionein protects human central nervous system cells and astrocytes from radiation-induced apoptosis. Toxicol. Lett. 2004, 146:217-226.
32. Lowicka E., Beltowski J. Hydrogen sulfide (H2S) - the third gas of interest for pharmacologists. Pharmacol. Rep. 2007, 59:4-24.
33. Levonen A.L., Lapatto R., Saksela M., Raivio K.O. Human cystathionine gamma-lyase: developmental and in vitro expression of two isoforms. Biochem. J. 2000, 347(Pt 1):291-295.
34. Papapetropoulos A., Pyriochou A., Altaany Z., Yang G., Marazioti A., Zhou Z., Jeschke M.G., Branski L.K., Herndon D.N., Wang R., Szabo C. Hydrogen sulfide is an endogenous stimulator of angiogenesis. Proc. Natl. Acad. Sci. U.S.A. 2009, 106:21972-21977.
35. Fan M., Ahmed K.M., Coleman M.C., Spitz D.R., Li J.J. Nuclear factor-kappaB and manganese superoxide dismutase mediate adaptive radioresistance in low-dose irradiated mouse skin epithelial cells. Cancer Res. 2007, 67:3220-3228.
36. Chankova S.G., Bryant P.E. Acceleration of DNA-double strand rejoining during the adaptive response of Chlamydomonas reinhardtii. Radiat. Biol. Radioecol. 2002, 42:600-603.
37. Kim S.K., Choi K.H., Kim Y.C. Effect of acute betaine administration on hepatic metabolism of S-amino acids in rats and mice. Biochem. Pharmacol. 2003, 65:1565-1574.
38. Yan G., Hua Z., Du G., Chen J. Adaptive response of Bacillus sp. F26 to hydrogen peroxide and menadione. Curr. Microbiol. 2006, 52:238-242.
39. Attene-Ramos M.S., Wagner E.D., Gaskins H.R., Plewa M.J. Hydrogen sulfide induces direct radical-associated DNA damage. Mol. Cancer Res. 2007, 5:455-459.
40. Yang G., Sun X., Wang R. Hydrogen sulfide-induced apoptosis of human aorta smooth muscle cells via the activation of mitogen-activated protein kinases and caspase-3. FASEB J. 2004, 18:1782-1784.
41. Miura Y. Oxidative stress, radiation-adaptive responses, and aging. J. Radiat. Res. (Tokyo) 2004, 45:357-372.
42. Matsumoto H., Takahashi A., Ohnishi T. Nitric oxide radicals choreograph a radioadaptive response. Cancer Res. 2007, 67:8574-8579.
43. Yuan D., Pan Y., Zhang J., Shao C. Role of nuclear factor-kappaB and P53 in radioadaptive response in Chang live cells. Mutat. Res. 2010, 688:66-71.
44. Pan T.T., Neo K.L., Hu L.F., Yong Q.C., Bian J.S. H2S preconditioning-induced PKC activation regulates intracellular calcium handling in rat cardiomyocytes. Am. J. Physiol. Cell Physiol. 2008, 294:C169-177.
45. Lee S.J., Choi S.A., Cho C.K., Kim T.H., Jeong K.S., Yoo S.Y., Lee Y.S. Adaptive response is differently induced depending on the sensitivity to radiation-induced cell death in mouse epidermal cells. Cell Biol. Toxicol. 2000, 16:175-184.
46. Kastan M.B., Lim D.S. The many substrates and functions of ATM. Nat. Rev. Mol. Cell Biol. 2000, 1:179-186.
47. Alexander A., Cai S.L., Kim J., Nanez A., Sahin M., MacLean K.H., Inoki K., Guan K.L., Shen J., Person M.D., Kusewitt D., Mills G.B., Kastan M.B., Walker C.L. ATM signals to TSC2 in the cytoplasm to regulate mTORC1 in response to ROS. Proc. Natl. Acad. Sci. U.S.A. 2010, 107:4153-4158.
48. Li L., Moore P.K. Putative biological roles of hydrogen sulfide in health and disease: a breath of not so fresh air?. Trends Pharmacol. Sci. 2008, 29:84-90.