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中华口腔医学研究杂志(电子版) ›› 2009, Vol. 3 ›› Issue (06) : 588 -592. doi: 10.3877/cma.j.issn.1674-1366.2009-06-003

基础研究

突变型Nbs1 基因转染对头颈癌放疗敏感性影响的实验研究
王代友1,(), 周诺1, 张斌1, 陆新萍1, 方首镕1, 蒋磊1   
  1. 1.530021 南宁,广西医科大学附属口腔医院口腔颌面外科
  • 收稿日期:2009-10-08 出版日期:2009-12-01
  • 通信作者: 王代友
  • 基金资助:
    广西自然科学基金资助(桂科自0640095)

The experimental study on enhancive radio-sensitivity of head & neck cancer cells after transfected with mutant Nbs1

Dai-you WANG1,(), Nuo ZHOU1, Bin ZHANG1, Xin-ping LU1, Shou-rong FANG1, Lei JIANG1   

  1. 1.Department of Oral and Maxillofacial Surgery, Hospital of Stomatology, Guangxi Medical University, Nanning 530021, China
  • Received:2009-10-08 Published:2009-12-01
  • Corresponding author: Dai-you WANG
引用本文:

王代友, 周诺, 张斌, 陆新萍, 方首镕, 蒋磊. 突变型Nbs1 基因转染对头颈癌放疗敏感性影响的实验研究[J/OL]. 中华口腔医学研究杂志(电子版), 2009, 3(06): 588-592.

Dai-you WANG, Nuo ZHOU, Bin ZHANG, Xin-ping LU, Shou-rong FANG, Lei JIANG. The experimental study on enhancive radio-sensitivity of head & neck cancer cells after transfected with mutant Nbs1[J/OL]. Chinese Journal of Stomatological Research(Electronic Edition), 2009, 3(06): 588-592.

目的

探讨突变型Nbs1 基因转染对头颈癌细胞放射敏感性的影响。

方法

用突变型Nbs1 腺病毒载体转染头颈癌细胞株JHU006,同时给予2 Gy Co60 γ 射线照射,24 h 后用MTT 法测定细胞生长曲线,以及中性彗星法检测癌细胞DNA 双链断裂程度。

结果

JHU006细胞株转染突变型Nbs1 基因并配合放射治疗后,癌细胞处于生长停滞状态;中性彗星实验显示,该组癌细胞平均尾力矩值明显增大。

结论

突变型Nbs1 基因转染可以抑制头颈部DNA双链断裂癌细胞的损伤修复功能,因而显著增加了癌细胞放疗敏感性。

Objective

To determine the radio-sensitivity of head & neck cancer cells after transfected with mutant Nbs1 gene.

Methods

JHU006 cells were transfected with mutant Nbs1 and then irradiated with 2 Gy of Co60 γ-ray for 24 hours. The MTT method was applied to determine the growth curve of head & neck cancer cells JHU006 and Neutral comet assay was used for observing the cells' DNA Double strain breaks.

Results

After the treatment, JHU006 cells growth was almost at a standstill and the values of the mean rail moment remarkably increased.

Conclusions

Transfected with mutant Nbs1 gene, Head & neck cancer cells' radiosensitivity significantly increased attribute to the inhibition of repair function for cancer cells DNA double strain breaks.

图1 细胞中性彗星结构示意图
图2 JHU006 转染突变型Nbs1 腺病毒后荧光显微镜观察
图3 JHU006 细胞不同组别间生长曲线
图4 正常对照组中性慧星检测结果
图5 单纯放射组中性慧星检测结果
图6 放射加Nbs1 转染组中性慧星检测结果
1
Olive PL, Wlodek D, Banath JP. DNA double-strand breaks measured in individual cells subjected to gel electrophoresis. Cancer Res,1991,151(17):4671-4676.
2
Helma C,Uhl M. A public domain image-analysis program for the single-cell gel-electrophoresis (comet) assay. Mutat Res, 2000,466(1):9-15.
3
Williams RS, Willams JS, Tainer JA. Mre11-Rad50-Nbs1 is a keystone complex connecting DNA repair machinery, double-strand break signaling, and the chromatin template. Biochem Cell Biol, 2007,85(4):509-520
4
Lavin MF. ATM and the Mre11 complex combine to recognize and signal DNA double-strand breaks. Oncogene, 2007,26(56):7749-7758.
5
Lee AY, Liu E, Wu X. The Mre11/Rad50/Nbs1 complex plays an important role in the prevention of DNA rereplication in mammalian cells. J Biol Chem, 2007,282(44):32243-32255.
6
Zhong ZH, Jiang WQ, Cesare AJ, et al. Disruption of telomere maintenance by depletion of the MRE11/RAD50/NBS1 complex in cells that use alternative lengthening of telomeres. J Biol Chem, 2007,282(40):29314-29322.
7
Lee JH, Paull TT. Activation and regulation of ATM kinase activity in response to DNA double-strand breaks. Oncogene, 2007,26(56):7741-7748.
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