Abstract Objective To investigate the radiobiological effects of radiation with different dose rates on human nasopharyngeal carcinoma cell line CNE-2 treated with or without a poly ADP-ribose polymerase (PARP) inhibitor,olaparib. Methods The concentration of olaparib used to treat cells equaled to the inhibition concentration IC10 of olaparib to CNE-2 cells. The CNE-2 cells were divided into acute radiotherapy (RT) group,fractionated radiotherapy (FRT) group,olaparib+RT group,and olaparib+FRT group. All groups were exposed to radiation of 0,1,2,3,5,7,and 10 Gy at a dose rate of 3 Gy/min.The delivery time for each dose point was 4 min in RT and 30 min in FRT.The colony forming assay was used to evaluate the survival of CNE-2 cells at each dose point. The multi-target,single-hit model was used to fit the cell survival curves and the parameters,D0,Dq,and SF2,were calculated. At dose points of 0,1,and 2 Gy,western blot was used to determine the expression of PARP-1 in the RT group and the FRT group and γH2AX in each group. Immunofluorescence was used to evaluate the γH2AX focus formation. A single factor analysis of variance was used to compare the 4 groups,and two two compared with SNK-q test. Results The IC10 value of olaparib to CNE-2 cells was4.0μmol/L.At dose points of 1 and 2 Gy,the PARP-1 expression was significantly higher in the FRT group than in the RT group (P=0.029,0.022),while the γH2AX focus number was significantly smaller in the FRT group than in the other three groups (all P<0.05);compared with the RT group,the D0,Dq,and SF2 values in the FRT group were increased by 11.67%,15.78%,and 23.61%,respectively;compared with the FRT group,the D0,Dq,and SF2 values in the Olaparib+FRT group decreased by 11.19%,6.44%,and 13.26%,respectively;there were no significant differences in above indices between the RT group,the Olaparib+RT group,and the Olaparib+FRT group. Conclusions For the same radiation dose,fractionation reduces the relative dose rate and weakens the radiobiological effects.low-dose olaparib can compromise the single strand break repair induced by the decline of the relative dose rate in a fractionated irradiation mode,which promotes the formation of double-strand break and improves the radiobiological effects.
Corresponding Authors:
Li Ming,Email:18323855734@163.com
Cite this article:
Zhao Gang,Huang Xiu,Zheng Taihao et al. Radiobiological effects of irradiation plus olaparib with different dose rates on CNE-2 cell line[J]. Chinese Journal of Radiation Oncology, 2016, 25(7): 764-769.
Zhao Gang,Huang Xiu,Zheng Taihao et al. Radiobiological effects of irradiation plus olaparib with different dose rates on CNE-2 cell line[J]. Chinese Journal of Radiation Oncology, 2016, 25(7): 764-769.
[1]杨伟志.电离辐射的细胞效应[A]//殷蔚伯,余子豪,徐国镇,等.肿瘤放射治疗学[M].4版.北京:中国协和医科大学出版社,2008:231-239. Yang WZH.Cell effect of ionizing radiation[A]//Yin WB,Yu ZH,Xu GZH,et al. Radiation oncology[M].4 ed. Beijing:Peking union medical college press,2008:231-239 [2]钱立庭,杨伟志,刘新帆.模拟IMRT模式的生物效应研究初探[J].中华放射肿瘤学杂志,2005,14(5):431-433.DOI:10.3760/j.issn:1004-4221.2005.05.014. Qian LT,Yang WZ,Liu XF.Preliminary study of radiobiological effects in intensity modulated radiation therapy model[J].Chin J Radiat Oncol,2005,14(5):431-433.DOI:10.3760/j.issn:1004-4221.2005.05.014 [3]Shrivastav M,De Haro LP,Nickoloff JA.Regulation of DNA double-strand break repair pathway choice[J].Cell Res,2008,18(1):134-147.DOI:10.1038/cr.2007.111 [4]Amé JC,Rolli V,Schreiber V,et al. Parp-2,a Novel Mammalian DNA damage-dependent poly (Adp-Ribose) polymerase[J].J Biol Chem,1999,274(25):17860-17868.DOI:10.1074/jbc.274.25.17860 [5]Johansson M.A human poly (Adp-Ribose) polymerase gene family (ADPRTL):cDNA cloning of two novel poly (Adp-Ribose) polymerase homologues[J].Genomics,1999,57(3):442-445.DOI:10.1006/geno.1999.5799 [6]Wang HY,Wang ML,Wang HC,et al. Complex H2AX phosphorylation patterns by multiple kinases including ATM and DNA-PK in human cells exposed to ionizing radiation and treated with kinase inhibitors[J].J Cell Physiol,2005,202(2):492-502.DOI:10.1002/jcp.20141 [7]Giunta S,Jackson SP.Give me a break,but not in mitosis:the mitotic DNA damage response marks DNA double-strand breaks with early signaling events[J].Cell Cycle,2011,10(8):1215-1221.DOI:10.4161/cc.10.8.15334 [8]Rothkamm K,Lbrich M.Evidence for a lack of DNA double-strand break repair in human cells exposed to very low x-ray doses[J].Proc Natl Acad Sci U S A,2003,100(9):5057-5062.DOI:10.1073/pnas.0830918100 [9]Fong PC,Boss DS,Yap TA,et al. Inhibition of poly (Adp-Ribose) POLYMERASE in Tumors from BRCA mutation carriers[J].N Engl J Med,2009,361(2):123-134.DOI:10.1056/NEJMoa0900212. [10]糜福顺.电离辐射DNA及染色体的作用[A]//沈瑜,糜福顺.肿瘤放射生物学[M].北京:中国医药科技出版社,2002:29-47. Mi FSH.Role of DNA and chromosome in ionizing radiation[A]//Shen Y,Mi FSH.Tumor radiation biology[M].Beijing:China medical science and technology publishing house,2002:29-47. [11]王东.基于DNA损伤修复的分子靶向治疗:肿瘤靶向治疗的新篇章[J].第三军医大学学报,2014,36(22):2243-2248.Wang D.Targeting DNA repair pathways:a new episode in targeted cancer therapeutics[J].J Third Milit Med Univ,2014,36(22):2243-2248. [12]Fernandez-capetillo O,Lee A,Nussenzweig M,et al. H2AX:the histone guardian of the genome[J].DNA Repair,2004,3(8-9):959-967.DOI:10.1016/j.dnarep.2004.03.024. [13]刘敏,赵苒.γH2AX检测在DNA双链断裂研究中应用[J].中国公共卫生,2015,31(6):742-746.DOI:10.11847/zgggws2015-31-06-14. Liu M,Zhao R.Application of γH2AX assay in measurement of DNA double stand breaks[J].Chin J Publ Health,2015,31(6):742-746.DOI:10.11847/zgggws2015-31-06-14. [14]Kuo LJ,Yang LX.Gamma-H2AX-a novel biomarker for DNA double-strand breaks[J].In Vivo,2008,22(3):305-309. [15]Paganetti H.Changes in tumor cell response due to prolonged dose delivery times in fractionated radiation therapy[J].Int J Radiat Oncol Biol Phys,2005,63(3):892-900.DOI:10.1016/j.ijrobp.2005.07.953. [16]王雯珺,郑小康,刘佳宾,等.鼻咽癌细胞株CNE1、HONE1、C666-1和CNE2的亚致死性损伤修复速度测定[J].南方医科大学学报,2010,30(4):777-778. Wang WJ,Zheng XK,Liu JB,et al. Determination of the repair half-time of human nasopharyngeal carcinoma cell lines CNE1,CNE2,HONE1 and C666-1[J].J South Med Univ,2010,30(4):777-778.