刘明珠,樊锐太,顾浩,等.小檗碱增强宫颈癌细胞放射敏感性的研究[J].中华放射医学与防护杂志,2017,37(8):581-586.Liu Mingzhu,Fan Ruitai,Gu Hao,et al.Effect of berberine on radiosensitivity of cervical cancer cells[J].Chin J Radiol Med Prot,2017,37(8):581-586
小檗碱增强宫颈癌细胞放射敏感性的研究
Effect of berberine on radiosensitivity of cervical cancer cells
投稿时间:2017-01-20  
DOI:10.3760/cma.j.issn.0254-5098.2017.08.004
中文关键词:  宫颈癌  小檗碱  放射敏感性  信号通路  细胞凋亡
英文关键词:Cervical cancer  Berberine  Radiosensitivity  Signaling pathway  Cell apoptosis
基金项目:福建省中青年骨干项目(2013-ZQN-ZD-8);福建省自然科学基金(2016J01437)
作者单位
刘明珠 450052 郑州大学第一附属医院中医科 
樊锐太 450052 郑州大学第一附属医院放疗科 
顾浩 450052 郑州大学第一附属医院放疗科 
王新杰 450052 郑州大学第一附属医院中医科 
刘艳杰 450052 郑州大学第一附属医院妇科 
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中文摘要:
      目的 探讨小檗碱对宫颈癌细胞凋亡及放射敏感性的影响。方法 用5、10、15、20 μmol/L的小檗碱作用于宫颈癌细胞Siha、HeLa、Caski记为给药组,同时以只加入二甲基亚砜(DMSO)的细胞为对照组,CCK-8法检测48 h细胞存活率,计算小檗碱半数抑制浓度。用半数抑制浓度的小檗碱作用于宫颈癌Siha细胞48 h,流式细胞术检测细胞凋亡率和细胞周期,Western blot检测细胞中活化的含半胱氨酸的天冬氨酸蛋白水解酶3(Cleaved Caspase-3)、细胞周期素B1(Cyclin Bl)、细胞周期蛋白依赖性激酶1(CDK1)、信号转导和转录因子(STAT)、磷酸化的STAT3(p-STAT3)表达水平。含有半数抑制浓度的小檗碱培养液培养宫颈癌Siha细胞24 h后,用0、2、4、6、8 Gy X射线照射细胞,细胞克隆形成实验检测放射敏感性。结果 小檗碱能够抑制宫颈癌细胞的生长,抑制作用从大到小为:Siha、Caski、HeLa,半数抑制浓度依次为(16.84±3.52)、(23.54±8.67)、(21.86±6.35)μmol/L。17 μmol/L的小檗碱能够促进宫颈癌细胞Siha凋亡(t=56.847,P<0.01),将细胞周期阻滞在G2/M期(t=47.251,P<0.01),并抑制宫颈癌细胞中Cyclin B1、CDK1、p-STAT3表达,促进Cleaved Caspase-3表达,对宫颈癌细胞中STAT3表达没有影响。17 μmol/L的小檗碱能够降低宫颈癌细胞的存活分数,放射增敏比为1.550。结论 小檗碱能够抑制宫颈癌细胞增殖,促进凋亡,阻滞细胞周期,增加宫颈癌细胞的放射敏感性。
英文摘要:
      Objective To investigate the effect of berberine on the radiosensitivity of cervical cancer cells. Methods 5, 10, 15, 20 μmol/L of berberine were used to treat cervical cancer cell lines of Siha, HeLa, Caski. DMSO was applied as control of drug treatment. Cell proliferation was detected by the CCK-8 method, and then the half inhibitory concentration of berberine was calculated. Cell apoptosis and cell cycle distribution were detected by flow cytometry. Protein expressions of Cleaved Caspase-3, Cyclin B1, CDK1, STAT3 and p-STAT3 were detected by Western blot. Cervical cancer cells of Siha were treated by berberine with a half inhibitory concentration for 24 h and then irradiated with 0, 2, 4, 6, 8 Gy of X-rays. Cell clone assay was used to detect cell survival. Results Berberine could inhibit the growth of cervical cancer cells with a half inhibition concentration of(16.84±3.52),(23.54±8.67),(21.86±6.35)μmol/L for Siha, Caski, and HeLa cells, respectively. The berberine at 17 μmol/L could induce apoptosis(t=56.847,P<0.01)and G2/M phase arrest(t=47.251,P<0.01)in Siha cells, which also inhibited the expressions of Cyclin B1, CDK1 and p-STAT3 and promoted the expression of cleaved Caspase-3, but did not influence the expression of STAT3 in cervical cancer cells. Treatment of cells with 17 μmol/L berberine increased the radiosensitivity of cervical cancer cells with a sensitivity enhancement ratio of 1.55. Conclusions Berberine can inhibit cell proliferation, promote apoptosis, block cell cycle, and increase radiosensitivity of cervical cancer cells.
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