苏富琴, 李洪燕,张翼, 侯书杰,雷平生,陈晓光. Icogenin对人胰腺癌BxPC3细胞侵袭转移能力的影响及机制研究J. 药学学报, 2009,44(5): 456-461.
引用本文: 苏富琴, 李洪燕,张翼, 侯书杰,雷平生,陈晓光. Icogenin对人胰腺癌BxPC3细胞侵袭转移能力的影响及机制研究J. 药学学报, 2009,44(5): 456-461.
SU Fu-Qin, LI Hong-Yan, ZHANG Yi, HOU Shu-Jie, LEI Beng-Sheng, CHEN Xiao-Guang. Effect of Icogenin on and its mechanism in anti-metastasis of pancreatic cancer BxPC3 cellsJ. 药学学报, 2009,44(5): 456-461.
Citation: SU Fu-Qin, LI Hong-Yan, ZHANG Yi, HOU Shu-Jie, LEI Beng-Sheng, CHEN Xiao-Guang. Effect of Icogenin on and its mechanism in anti-metastasis of pancreatic cancer BxPC3 cellsJ. 药学学报, 2009,44(5): 456-461.

Icogenin对人胰腺癌BxPC3细胞侵袭转移能力的影响及机制研究

Effect of Icogenin on and its mechanism in anti-metastasis of pancreatic cancer BxPC3 cells

  • 摘要:

    观察Icogenin对人胰腺癌BxPC3细胞的体外抗转移作用,并对其作用机制进行探讨。采用穿膜方法、改良MTT法和单层细胞划痕实验观察IcogeninBxPC3细胞侵袭、黏附和运动能力的影响。Western blotting法检测IcogeninMAPK信号转导通路蛋白表达的变化,明胶酶法分析其对MMP2分泌的影响。结果显示,Icogenin在体外可显著抑制人胰腺癌BxPC3细胞的侵袭、运动以及黏附作用 (P < 0.05),并呈较好的剂量依赖关系,ERK抑制剂PD98059U0126也可抑制侵袭转移。Icogenin可抑制MMP2的分泌,同时可抑制MAPK信号转导通路中的ERK磷酸化。因此认为Icogenin在体外具有一定的抑制胰腺癌细胞侵袭迁移的作用,其机制与抑制MMP2分泌和抑制ERK磷酸化有关。

     

    Abstract:

    This study is to investigate the effect of Icogenin on and its mechanism in anti-metastasis of pan- creatic cancer BxPC3 cells in vitro.  Using transwell assay, the effects of Icogenin on the invasion of BxPC3 cells were measured.  The abilities of cell motility and adhesion in BxPC3 cells were detected by MTT assay and wound healing assay, respectively.  The MAPK signal pathway protein expressions were analyzed with Western blotting.  Also, the activity of MMP2 was observed by zymography assay.  Icogenin inhibited the abilities of motility, adhesion and invasion of pancreatic cancer BxPC3 cells in vitro (P < 0.05), in a dose-depended manner, and inhibited the secretion of MMP2 and phosphorylation of ERK.  PD98059 and U0126 which were ERK   inhibitors could suppress the abilities of invasion and metastasis of pancreatic cancer BxPC3 cells.  It is    concluded that Icogenin can inhibit the abilities of invasion and metastasis of pancreatic cancer in vitro by    inhibiting the secretion of MMP2 and phosphorylation of ERK.

     

/

返回文章
返回