临床肿瘤学杂志

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汉防己甲素对人肺腺癌细胞的放射增敏作用及其机制的实验研究

丁 巍1,杨爱珍2,徐海军2,陈龙华3

  

  1. 1 210002 南京 解放军八一医院全军肿瘤中心放疗科2 210002 解放军八一医院全军肿瘤中心实验科3 510515南方医科大学附属南方医院放疗科
  • 收稿日期:2015-11-13 修回日期:2016-02-02 出版日期:2016-05-31 发布日期:2016-05-31
  • 通讯作者: 陈龙华

Effects of tetrandrine on radiosensitvity of lung adenocarcinoma cell line and it’s mechanism

DING Wei, YANG Aizhen, XV Haijun, CHEN Longhua.

  

  1. Department of Radiotherapy, PLA Cancer Center, Bayi Hospital, Nanjing 210002, China
  • Received:2015-11-13 Revised:2016-02-02 Online:2016-05-31 Published:2016-05-31
  • Contact: CHEN Longhua

摘要: 目的 探讨汉防己甲素(Tet)对人肺腺癌SPC-A1细胞的放射敏感性的影响及其作用机制。方法 MTT法检测Tet对SPC-A1细胞的增殖抑制作用,比较单纯照射组(4 Gy)、照射(4 Gy)+Tet(1 μmol/L)组、单用Tet组(1 μmol/L)及空白对照组间SPC-A1细胞增殖抑制率的差异。采用克隆形成实验来计算受照射后的细胞存活率,拟合细胞存活曲线,计算D0、Dq、SF2。流式细胞术检测照射前后SPC-A1细胞周期的分布情况。结果 Tet对SPC-A1细胞的24、48和72 h半数抑制浓度(IC50)分别为10.77、5.78、和3.89 μmol/L。照射+Tet组24、48、72 h的细胞增殖抑制率均高于单纯照射组,差异有统计学意义(P<0.05)。克隆形成实验显示照射+Tet组的D0、Dq和SF2值分别为(1.551±0.045)Gy、(0.522±0.023)Gy和0.503±0.008,均低于单纯照射组。放射增敏比(SER)为1.48。流式细胞仪检测结果显示照射导致了SPC-A1细胞G2期阻滞(P<0.05)。联合Tet后可以降低G2期阻滞细胞比例(P<0.05)。结论 Tet可以有效增加人肺腺癌SPC-A1细胞的放射敏感性,其机制可能是通过降低放射导致的G2期阻滞细胞比例,从而使DNA的损伤固定,发生增殖性死亡。

Abstract: Objective To investigate the effects of tetrandrine(Tet) on radiosensitivity of human lung adenocarcinoma SPC-A1 cells and its mechanism. Methods MTT assay was used to evaluate the cytotoxicity of Tet on SPC-A1. MTT assay were used to evaluate the inhibition ratio of irradiation group(X-ray 4 Gy), Tet (1 μmol/L)+irradiation (X-ray 4 Gy) group and Tet group (1 μmol/L). Cell viability after radiation was calculated by clonogenic assay. According to cell survival curve, the parameters including D0, Dq,SF2 were calculated. Flow cytometry was used to detect the cell cycle distribution of irradiation group and Tet+irradiation group. Results The IC50 of Tet on SPC-A1 cells at 24, 48 and 72 h were 10.77, 5.78 and 3.89 μmol/L, respectively. The values of D0,Dq,and SF2 of Tet+irradiation group were(1.551±0.045)Gy, (0.522±0.023)Gy and 0.503±0.008, which were lower than those of irradiation group, and SER was 1.48. Flow cytometry showed that exposure of SPC-A1 cells to 4 Gy of Xrays caused G2/M arrests (P<0.05). The arrests were abrogated by treated with Tet(P<0.05). Conclusion Tet can efficiently enhance the radiosensitivity of SPC-A1 cell. The mechanism maybe abrogating the radiation-induced G2 phase arrest. It fixes the damage of DNA,and causes reproductive cell death.

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