刘建兵, 戚梦, 李巧琪, 李佳欢, 胡开辉, 林文雄, 傅俊生. 虫草素抑制胰腺癌干细胞增殖及转移的机制研究J. 药学学报, 2017,52(9): 1404-1409. doi: 10.16438/j.0513-4870.2017-0353
引用本文: 刘建兵, 戚梦, 李巧琪, 李佳欢, 胡开辉, 林文雄, 傅俊生. 虫草素抑制胰腺癌干细胞增殖及转移的机制研究J. 药学学报, 2017,52(9): 1404-1409. doi: 10.16438/j.0513-4870.2017-0353
LIU Jian-bing, QI Meng, LI Qiao-qi, LI Jia-huan, HU Kai-hui, LIN Wen-xiong, FU Jun-sheng. The mechanism of cordycepin in inhibition of pancreatic cancer stem cells proliferation and metastasisJ. Acta Pharmaceutica Sinica, 2017,52(9): 1404-1409. doi: 10.16438/j.0513-4870.2017-0353
Citation: LIU Jian-bing, QI Meng, LI Qiao-qi, LI Jia-huan, HU Kai-hui, LIN Wen-xiong, FU Jun-sheng. The mechanism of cordycepin in inhibition of pancreatic cancer stem cells proliferation and metastasisJ. Acta Pharmaceutica Sinica, 2017,52(9): 1404-1409. doi: 10.16438/j.0513-4870.2017-0353

虫草素抑制胰腺癌干细胞增殖及转移的机制研究

The mechanism of cordycepin in inhibition of pancreatic cancer stem cells proliferation and metastasis

  • 摘要: 研究虫草素在体外抑制胰腺癌干细胞增殖及转移作用,并初步探讨其作用机制。MTT法检测不同浓度虫草素对胰腺癌干细胞的增殖抑制作用;倒置显微镜观察细胞的形态变化;碘化丙啶(PI)单染法检测虫草素的凋亡诱导作用;细胞划痕愈合实验检测细胞迁移能力;RT-PCR和Western blot检测细胞凋亡基因及细胞上皮间充质转化(epithelial-mesenchymal transition,EMT)相关基因的表达水平。结果表明,虫草素对胰腺癌干细胞具有显著增殖抑制及凋亡诱导作用,24和48 h的半数有效抑制浓度(IC50)分别为107.364和48.472 μmol·L-1;细胞划痕愈合实验发现虫草素能抑制细胞的迁移能力;对凋亡相关基因及蛋白的分析发现,虫草素处理胰腺癌干细胞后,抗凋亡基因Bcl-2表达下调,促凋亡基因Bax表达上调,同时检测到caspase-3和p53被显著激活;进一步对细胞EMT相关基因分析发现,60 μmol·L-1虫草素作用24 h后,E-cadherin表达被上调,N-cadherin表达下调,相对表达量分别为2.19和0.36。可见,虫草素不仅有效抑制胰腺癌干细胞增殖和诱导凋亡,还能明显减弱其迁移能力,并提示其作用机制可能与激活p53信号通路与逆转肿瘤细胞EMT有关,这为靶向胰腺癌干细胞治疗胰腺癌提供新的思路和理论基础。

     

    Abstract: To investigate the effects of cordycepin on proliferation and invasion of pancreatic cancer stem cells (Pan CSC) and its mechanisms, MTT assay was used to investigate the effect of cordycepin on proliferation of Pan CSC. Inverted microscope was used to observe the morphologic change of cells. Propidium iodide staining methods was employed to observe the cell apoptosis. Cell scratch method was used to detect the ability of migration of Pan CSC in each group. RT-PCR and Western blot were used to determine the expression of apoptosis gene and epithelial-mesenchymal transitions (EMT) gene. The growth of Pan CSC was inhibited by cordycepin in a dose-and time-dependent manner, with IC50 107.364 and 48.472 μmol·L-1 at 24 and 48 h, respectively. Moreover, the cell migration was inhibited at the same time. RT-PCR and Western blot results showed that cordycepin decreased the expression of Bcl-2 and activated pro-apoptotic gene levels such as Bax,p53, caspase-3. Furthermore, cordycepin reduced the expression of EMT genes by up-regulation of E-cadherin and down-regulation of N-cadherin. Cordycepin has the ability to inhibit Pan CSC proliferation and invasion by activating p53 pathway as well as suppressing the EMT. This study provides a new basis for inhibition of pancreatic cancer stem cells in the treatment of pancreatic cancer.

     

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