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Effect of p53 on lung carcinoma cells irradiated by carbon ions or X-rays

LOW ENERGY ACCELERATOR AND RADIATION APPLICATIONS

Effect of p53 on lung carcinoma cells irradiated by carbon ions or X-rays

XIE Yi
ZHANG Hong
HAO Jifang
ZHAO Weiping
WU Zhenhua
QIU Rong
WANG Xiaohu
Nuclear Science and TechniquesVol.20, No.3pp.146-151Published in print 20 Jun 2009
43500

The study is to investigate the feasibility and advantages of heavy ion beams on radiotherapy. The cellular cycle and apoptosis, cell reproductive death and p53 expression evaluated with flow cytometry, clonogenic survival assays and Western blot analysis were examined in lung carcinoma cells after exposure to 89.63 MeV/u carbon ion and 6 MV X-ray irradiations, respectively. The results showed that the number colonyforming assay of A549 was higher than that of H1299 cells in two radiation groups; A549 cellular cycle was arrested in G2/M in 12 h and the percentage of apoptosis ascended at each time point of carbon ion radiation with doses, the expression of p53 upregulated with doses exposed to X-ray or carbon ion. The cell number in G2/M of H1299 and apoptosis were increasing at all time points with doses in 12C6+ ion irradiation group. The results suggested that the effects of carbon ions or X rays irradiation on lung carcinoma cells were different, 12C6+ ion irradiation could have more effect on upregulating the expression of p53 than X-ray, and the upregulated expression of p53 might produce the cellular cycle G2/M arrested, apoptosis increasing; and p53 gene might affect the lung cancer cells radiosensitivity.

12C6+ ion irradiationExpression of p53Cellular cycle and apoptosisSurvival of cellsX-ray
References
[1] Dikomey E, Borgmann K, Brammer I et al. Toxicology, 2003, 193(1-2): 125-135.
[2] Distel LV, Neubauer S, Keller U et al. Radiother Oncol, 2006, 81(3): 257-263.
[3] Peacock J H, Edwards H A, Mcmillan T R et al. Int J Radiat Biol, 1989, 56(5): 543-547.
[4] Komarova E A, Chernov M V, Franks R, et al. EMBO J, 1997, 16(6): 1391-1400.
[5] Frenkel J, Sherman D, Fein A, et al. Oncogene, 1999, 18(18): 2901-2907.
[6] Komarova E A, Gudkov A V. Biochemistry (Mosc), 2000, 65(1): 41-48.
[7] Vanparys C, Maras M, Lenjou M, et al. Coen Toxicol in Vitro, 2006, 20(7): 1238-1248.
[8] Farmer G, Bargonetti J, Zhu H, et al. Nature, 1992, 358(6381): 83-86.
[9] El-Deiry W S, Tokino T, Velculescu V E, et al. Cell, 1993, 75(4): 817-825.
[10] Harper J W, Adami G R, Wei N, et al. Cell, 1993, 75(4): 805-816.
[11] Xiong Y, Hannon GJ, Zhang H, et al. Nature, 1993, 366(6456): 701-704.
[12] Vousden K H. Cell, 2000, 103(5): 691-694.
[13] Vogelstein B, Lane D, Levine A J. Nature, 2000, 408(6810): 307-310.
[14] Deng Y, Wu X. Proc Natl Acad Sci U. S. A, 2000, 97(22): 12050-12055.
[15] Brugarolas J, Chandrasekaran C, Gordon J I, et al. Nature, 1995, 377(6549): 552-557.
[16] Harris M P, Sutjipto S, Wills K N, et al. Cancer Gene Ther, 1996, 3(2): 121-130.
[17] Nielsen L L, Maneval D C. Cancer Gene Ther, 1998, 5(1): 52-63.
[18] Colletier P J, Ashoori F, Cowen D, et al. Int J Radiat Oncol Biol Phys, 2000, 48(5): 1507-1512.
[19] Koizumi H, Taguchi M, Kobayashi Y, et al. Instrum Method Phys Res, Sect B, 2003, 208(43): 161-165.