卢 文,杨艳梅,马敬全.自噬在熊果酸抑制人宫颈癌HeLa细胞增殖中的作用[J].中国肿瘤,2016,25(7):553-558.
自噬在熊果酸抑制人宫颈癌HeLa细胞增殖中的作用
Role of Autophagy in Ursolic Acid Inhibiting Human Cervical Cancer HeLa Cells Proliferation
投稿时间:2016-01-07  
DOI:10.11735/j.issn.1004-0242.2016.07.A011
中文关键词:  熊果酸  自噬  宫颈癌  p62  Beclin-1  3-MA
英文关键词:ursolic acid  autophagy  cervical carcinoma  p62  Beclin-1  3-MA
基金项目:黑龙江省自然科学基金(D201136);黑龙江省博士后科学研究基金(LBH-Z06252)
作者单位
卢 文 哈尔滨医科大学附属肿瘤医院 
杨艳梅 哈尔滨医科大学肿瘤研究所 
马敬全 哈尔滨医科大学附属肿瘤医院 
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中文摘要:
      摘 要:[目的] 分析自噬在熊果酸抑制人宫颈癌HeLa细胞增殖中的作用。[方法]体外培养人宫颈癌HeLa细胞,不同浓度(5、10、20 μmol/L)的熊果酸处理48h后,采用MTT法检测HeLa细胞增殖抑制率的变化;透射电镜观察细胞自噬超微结构的改变;Western blotting检测自噬相关蛋白p62及Beclin-1的表达情况;微管相关蛋白1轻链3A/B(microtubule-associated protein 1 light chain 3 A/B,LC3A/B)免疫荧光检测熊果酸对HeLa细胞自噬水平的影响;检测自噬抑制剂3-甲基腺嘌呤(3-methyladenine,3-MA)抑制自噬前后对熊果酸增殖抑制作用的影响。[结果] 不同浓度(5、10、20 μmol/L)的熊果酸处理组对HeLa细胞的抑制率分别为20.1 %±1.3 %、35.6 %±2.6 %和49.0 %±1.0 %,熊果酸可抑制HeLa细胞增殖并呈剂量依赖性(F=446.177,P<0.001);熊果酸能诱导HeLa细胞发生自噬:透射电镜观察发现经熊果酸处理后HeLa细胞中自噬囊泡明显增加;Western blotting分析表明熊果酸可呈剂量依赖性增加Beclin-1的表达,降低p62的表达;免疫荧光检测显示熊果酸处理后,HeLa细胞的荧光强度与对照组相比明显增强;3-MA与熊果酸联合作用于HeLa细胞时可抑制细胞增殖。[结论]熊果酸抑制HeLa细胞增殖,并诱导其发生自噬,自噬抑制剂3-MA能够增强熊果酸对HeLa细胞的增殖抑制作用。
英文摘要:
      Abstract:[Purpose] To investigate the role of autophagy in the proliferation inhibition to HeLa cells by ursolic acid(UA).[Methods]Human cervical cancer HeLa cells were cultured in vitro with various concentrations(5,10,20 μmol/L) of UA for 48h and the proliferation inhibition rate of HeLa cells was detected by MTT method. The change of ultrastructure was observed under transmission electronic microscope(TEM). The expressions of autophagy-associated proteins in HeLa cells treated with UA were determined by fluorescent staining of microtubule-associated protein 1 light chain 3A/B(LC3A/B). The protein levels of autophagy-associated protein p62 and Beclin-1 were detected by Western blotting analysis. Detect the impact to cell proliferation inhibition after autophagy inhibitor 3-methyladenine (3-MA) inhibited autophagy in HeLa cells. [Results]The inhibition rate in 5,10 and 20μmol/L UA group was 20.1%±1.3%,35.6%±2.6% and 49.0%±1.0%,UA at various concentrations showed significantly proliferationinhibition of HeLa cells in a dose-dependent manner. Autophagy was induced in HeLa cells treated with UA as observed by TEM that autophagic vesicles were strikingly increased in HeLa cells. Western blotting analysis showed that UA aroused a dose-dependent increase in the expression of Beclin-1 and reduced the expression of p62. The fluorescent density of LC3A/B positive in HeLa cells increased significantly as compared with those in control group. 3-MA+UA remarkablely decreased HeLa cell viability. [Conclusions] UA can inhibit HeLa cell proliferation and induce autophagy. Autophagy inhibitor 3-MA can enhance the proliferation inhibition of UA to HeLa cells.
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