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下调ATM表达对喉鳞状细胞癌放射敏感性影响的体内研究 被引量:2

Effect of down-regulating expression of ataxia telangiectasia mutated on radiosensitivity to laryngeal squamous cell carcinoma in vivo
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摘要 目的设计反义ATM(共济失调毛细血管扩张症突变基因)多核苷酸作用于裸鼠移植瘤以探讨其对喉鳞状细胞癌(Hep-2)放射治疗敏感性的影响。方法①雌性BALB/c-nu/nu裸鼠,分成对照组、ATM AS-ODNs(ATM反义多核苷酸)组、单独放疗组、ATM AS-ODNs+放疗4组(联合治疗组),每组8只,于裸鼠背侧部皮下注射105个Hep-2细胞悬液并对各组进行相应处理;②3周后用Western blot对各组瘤体的ATM蛋白进行分析;③用TUNEL染色法检测各组瘤体中细胞凋亡情况。结果①与ATM AS-ODNs组比较,AS-ODNs+放疗组的ATM蛋白表达量降低[(76.84±3.12)%vs(48.19±3.98)%,P<0.05]。②ATM AS-ODNs+放疗组的细胞凋亡数显著高于单独放疗组、AS-ODNs组及对照组[(17.12±4.2)%vs(8.17±3.5)%,(4.13±2.3)%,(3.09±5.3)%],差异有统计学意义。③采用AS-ODNs+放疗组的肿瘤生长较ATM AS-ODNs组、放疗组及对照组慢。结论反义ATM多核苷酸在体内增强了喉鳞状细胞癌对放射治疗的敏感性。 Objective To investigate the effect of the antisense polynucleotide(AS-ODNs)targeting ataxia telangiectasia mutated(ATM)on radiosensitivity to the transplanted tumors of nude mice in laryngeal squamous cell carcinoma cell line(Hep-2).Methods ①Female BALB/c-nu/nu mice were randomized into four groups(n=8 in each group).The mice were treated with normal saline in control group and ATM AS-ODNs alone in ATM ASODNs group.The mice were exposed to X-ray of 2 Gy alone in radiation group,while in ATM AS-ODNs+radiotherapy group,2.5 mg/kg of ATM AS-ODNs was injected into the solid tumor the day before exposure to 2 Gy X-ray,and repeated again at an interval of 5 d for each time.About 1×105 Hep-2 cells were subcutaneously inoculated in dorsal space of the mice.②The expression of ATM protein in tumor was examined by Western blot in four groups after 3 weeks.③TUNEL assay was used to analyze the cell apoptosis in the tumors of nude mice.Results ①The ATM protein expression in AS-ODNs+radiotherapy group was significantly lower than that in AS-ODNs group [(48.19±3.98)% vs(76.84±3.12)%,P0.05].②The apoptotic cells was statistically higher in AS-ODNs+radiotherapy group than those in the other groups(P0.05).③Tumor growth rate was slower in AS-ODNs+radiotherapy group than that of ATM AS-ODNs group,radiation group and control group.Conclusion ATM AS-ODNs could strengthen the radiosensitivity of laryngeal cell carcinoma in vivo.
出处 《山西医科大学学报》 CAS 2013年第2期127-130,F0003,共5页 Journal of Shanxi Medical University
基金 国家自然科学基金资助项目(30872850) 四川省教育厅基金资助项目(12ZA054) 川北医学院科研发展计划基金资助项目(CBY11-A-ZP08)
关键词 ATM 反义ATM 放射敏感性 喉鳞状细胞癌 ataxia telangiectasia mutated(ATM) ATM AS-ODNs radiosensitivity laryngeal squamous cell carcinoma
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参考文献9

  • 1Parkin DM, Bray F, Ferlay J, et al. Global cancer statistics [ J ]. CA Cancer J Clin,2005,55(2) :74 - 108.
  • 2Lei L, Michael S, Randy JL. Cellular responses to ionizing radia- tion damage [ J]. Int J Radiat Oncol Biol Phys, 2001,49 (4) : 1157 - 1162.
  • 3Lin CS, Wang YC, Huang JL, et al. Autophagy and reactive oxy- gen species modulate cytotoxicity induced by suppression of ATM kinase activity in head and neck cancer cells [ J ]. Oral Oncol, 2012,48 ( 11 ) : 1152 - 1158.
  • 4Liu S, Opiyo SO, Manthey K, et al. Distinct roles for DNA-PK, ATM and ATR in RPA phosphorylation and checkpoint activation in response to replication stress [ J]. Nucl Acid Res, 2012, g0 (21) : 10780 - 10794.
  • 5Parsons JL, Khorenenkova SV, Irina II, et al. Phosphorylation of PNKP by ATM prevents its preteasomal degradation and enhances resistance to oxidative stress [ J ]. Nucl Acid Res,2012,31 (5) : 1 -12.
  • 6Adams KE,Medhurst AL,Dart DA,et al. Recruitment of ATR to sites of ionising radiation-induced DNA damage requires ATM and components of the MRN protein complex [ J ]. Oncogene, 2006,25 (28) :3894 - 3904.
  • 7Zou J, Qiao X, Ye H, et al. Antisense inhibition of ATM gene en- hances the radiosensitivity of head and neck squarnous cell carci- noma in mice [ J ]. J Exp Clin Cancer Res,2008,27 (56) : 1 - 11.
  • 8江继平,冯俊,唐嗣泉,刘世喜.反义ATM在体外对喉鳞状细胞癌ATM蛋白表达影响的研究[J].川北医学院学报,2011,26(5):394-396. 被引量:3
  • 9李丽,冯俊,王朝莉,敬保迁.反义ATM多核苷酸对喉鳞状细胞癌ATM mRNA、蛋白影响的体外研究[J].川北医学院学报,2012,27(5):438-440. 被引量:2

二级参考文献15

  • 1LEI L, MICHAEL S, RANDY JL. Cellular responses to ionizing radiation damage [J]. Int J Radiat Oncol Biol Phys, 2001,(49) :1157 - 1162.
  • 2Akman FC, Dag N, Ataman OU, et al. The impact of treatment center on the outcome of patients with laryngeal cancer treated with surgery and radiotherapy [J]. Eur Arch Otorhinolaryngol, 2008,265 ( 10 ) : 1245 - 1255.
  • 3Smith RB. Surgery in the management of laryngeal and hypopharyngeal carcinoma[J]. International journal of radiation oncology,2007, 69(2 Suppl) :28 -30.
  • 4Hristov B, Bajaj GK. Radiotherapeutic management of laryngeal carcinoma[J]. Otolaryngologic clinics of North America, 2008,41(4) :715 -740.
  • 5Rodemann HP, Blaese MA. Responses of normal cells to ionizing radiation[J]. Seminars in radiation oncology ,2007, 17(2) :81 -88.
  • 6Choi EK, Ji IM, Lee SR,et al. Radiosensitization of tumor cells by modulation of ATM kinase[J]. International journal of radiation biology, 2006, 82(4):277-283.
  • 7Zou Jian, Qiao Xiaoming, Ye Huiping, et al. Antisense inhibition of ATM gene enhances the radiosensitivity of head and neck squamous cell carcinoma in mice[J]. Journal of Experimental & Clinical Cancer Research,2008, (27) :56.
  • 8Lei L, Michael S, Randy JL. Cellular responses to ionizing radiation damage [ J ]. Int J Radiat Oncol Biol Phys, 2001,49 ( 4 ) : 1157 - 1162.
  • 9Bartkova J, Horejsl Z, Koed K, et al. DNA damage response as acandidate anti-cancer barrier in early human tumorigenesis [ J ]. Nature ,2005,434 (7035.) : 864 - 870.
  • 10Gorgoulis VG, Vassiliou LV, Karakaidos P, et al. Activation of the DNA damagecheckpoint and genomic instability in human precan- cerous lesions[ J]. Nature ,2005,434 ( 7035 ) :907 - 913.

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同被引文献43

  • 1王春刚,韩玲,张晓青,郁成雨,唐古生,姚雨石.RNA干扰抑制胰腺癌细胞DNA-PKcs基因表达对放射敏感性的影响[J].胰腺病学,2006,6(2):88-91. 被引量:6
  • 2庄亮,于世英,黄晓园,曹阳,熊慧华.DNA-PKcs、Ku80及ATM备选宫颈癌放疗增敏靶点的体外研究[J].癌症,2007,26(7):724-729. 被引量:19
  • 3庄亮,于世英,黄晓园,熊慧华,熊华,李小兰,冷彦.Ku80表达抑制细胞模型的建立及其功能检测[J].中华放射医学与防护杂志,2007,27(5):447-450. 被引量:3
  • 4Awada A, Mano M, Hendlisz A, et al. New anticancer agents and therapeutic strategies in development for solid cancers: A clinical perspective [J]. Expert Rev Anticaneer Ther, 2004, 4( 1 ) : 53-60.
  • 5Ashihara E, Kawata E, Maekawa T. Future prospect of RNA in- terference for cancer therapies [J]. Curr Drug Targets, 2010, 11 (3) : 345-360.
  • 6Holoch D, Moazed D. RNAi in fission yeast finds new targets and new ways of targeting at the nuclear periphery [ J ]. Genes Dev, 2012, 26(8) : 741-745.
  • 7Carthew RW, Sontheimer EJ. Origins and mechanisms of miRNAs and siRNAs [J]. Cell, 2009, 136(4) : 642-655.
  • 8Masiero M, Nardo G, Indraccolo S, et al. RNA interference: Im- plications for cancer treatment [ J ]. Mol Aspects Med, 2007, 28 ( 1 ) : 143-166.
  • 9Rual JF, Klitgord N, Achaz G. Novel insights into RNAi off-target effects using C. elegans paralogs [J]. BMC Genomics, 2007, 8: 106.
  • 10Manjunath N, Dykxhoorn DM. Advances in synthetic siRNA de- livery [J]. Discov Med, 2010, 9(48) : 418-430.

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