孙菲,孙志强,汪建林,等.阿帕替尼对食管癌Kyse-150细胞放射敏感性影响的实验研究[J].中华放射医学与防护杂志,2017,37(11):805-809,831.Sun Fei,Sun Zhiqiang,Wang Jianlin,et al.Radiosensitizing effect of apatinib on esophageal cancer cell line Kyse-150[J].Chin J Radiol Med Prot,2017,37(11):805-809,831
阿帕替尼对食管癌Kyse-150细胞放射敏感性影响的实验研究
Radiosensitizing effect of apatinib on esophageal cancer cell line Kyse-150
投稿时间:2017-06-25  修订日期:2017-06-25
DOI:10.3760/cma.j.issn.0254-5098.2017.11.001
中文关键词:  食管癌  放射敏感性  阿帕替尼  细胞凋亡  细胞周期
英文关键词:Esophageal cancer  Radiosensitivity  Apatinib  Apoptosis  Cell cycle
基金项目:国家自然科学基金(11705095)
作者单位E-mail
孙菲 213003 南京医科大学附属常州第二人民医院放疗科  
孙志强 213003 南京医科大学附属常州第二人民医院放疗科  
汪建林 213003 南京医科大学附属常州第二人民医院放疗科  
王坚 213003 南京医科大学附属常州第二人民医院放疗科  
胡莉钧 213003 南京医科大学附属常州第二人民医院放疗科  
周梦耘 213003 南京医科大学附属常州第二人民医院放疗科  
封悦 213003 南京医科大学附属常州第二人民医院放疗科  
孔泽 213003 南京医科大学附属常州第二人民医院放疗科  
华秋 213003 南京医科大学附属常州第二人民医院放疗科  
于静萍 213003 南京医科大学附属常州第二人民医院放疗科 yujingping700420@sina.com 
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中文摘要:
      目的 观察阿帕替尼对食管癌Kyse-150细胞放射敏感性的影响,并初步探讨其作用机制。方法 将食管癌Kyse-150细胞分为空白对照组、阿帕替尼组、单纯照射组、阿帕替尼联合照射组。CCK-8法检测不同浓度阿帕替尼(0、5、10、20、30、40 μmol/L)对细胞增殖的影响;克隆形成法检测不同浓度阿帕替尼(0、10、20、40 μmol/L)对细胞放射敏感性的影响;流式细胞术分析阿帕替尼(20 μmol/L)联合射线(4 Gy)对细胞周期和细胞凋亡的影响。结果 阿帕替尼能抑制Kyse-150细胞的增殖,且呈剂量-时间依赖性(r=0.89~0.96,P<0.05);随着阿帕替尼浓度的增加,Kyse-150细胞的放射生物学参数D0DqSF2值逐渐减小,而放射增敏比SERD0值逐渐增加。阿帕替尼联合照射组分别与空白对照组、单纯照射组及阿帕替尼组比较,细胞凋亡率均显著增加,差异具有统计学意义(t=12.36、5.99、15.47,P<0.05)。与空白对照组比较,阿帕替尼组、单纯照射组及阿帕替尼联合照射组G2/M期比例均增高,差异均具有统计学意义(t=8.81、39.69、20.61,P<0.05)。阿帕替尼组、阿帕替尼联合照射组分别与空白对照组及单纯照射组相比,S期比例均增高,差异均具有统计学意义(t=6.06、3.82、8.81、6.24,P<0.05)。而阿帕替尼组与阿帕替尼联合照射组相比,S期比例差异无统计学意义(P> 0.05)。结论 阿帕替尼能增加食管癌Kyse-150细胞的放射敏感性,其机制可能与抑制细胞增殖、促进细胞凋亡及诱导细胞周期再分布有关。
英文摘要:
      Objective To evaluate the radiosensitization effect of apatinib on esophageal cancer cell line Kyse-150, and to investigate the underlying mechanism. Methods Cells were divided into four groups:control group, apatinib treatment group, X-ray radiation group, and the combination group treated with X-rays plus apatinib. The effect of apatinib with different concentrations on the cell proliferative and radiosensitivity were evaluated by CCK-8 kit and colony formation assay. Flow cytometry method was adopted to detect the effect of apatinib on cell cycle progress and apoptosis induction. Results Apatinib inhibited the proliferation of Kyse-150 cells in time-and dose-dependent manners (r=0.89-0.96, P<0.05). With the increase of apatinib concentration, D0, Dq and SF2 value of Kyse-150 cells decreased and SERD0 value increased. Compared with control group, apatinib alone group, and radiation alone group, the cell apoptosis rate significantly increased in the combination group (t=12.36, 5.99, 15.47,P<0.05). Compared with control group, the percentages of cells in G2/M phase were all significantly increased in apatinib group, radiation group and combination group (t=8.81, 39.69, 20.61,P<0.05). Compared with radiation alone group and control group, the percentage of cells in S phase significantly increased in apatinib alone group and combination group(t=6.06, 3.82,8.81,6.24,P<0.05). ConclusionsApatinib can increase radiosensitivity of esophageal cancer cell line Kyse-150 possibly by inhibiting cell proliferation, inducing cell apoptosis and causing redistribution of cell cycle.
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