南方医科大学学报 ›› 2015, Vol. 35 ›› Issue (08): 1110-.

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原花青素上调let-7a抑制胰腺癌AsPC-1细胞生长及迁移

马佳,方斌斌,马聪,庞海杰,曾凡鹏,夏俊   

  • 出版日期:2015-08-20 发布日期:2015-08-20

Proanthocyanidins inhibit pancreatic cancer AsPC-1 cell growth and migration through
up-regulation of let-7a

  • Online:2015-08-20 Published:2015-08-20

摘要: 目的探讨原花青素是否通过上调let-7a表达而抑制胰腺癌细胞生长及迁移。方法体外培养人胰腺癌AsPC-1细胞,原花
青素处理细胞后,分别用MTT法、Annexin V-FITC/PI双染及Transwell迁移等实验检测细胞增殖率、细胞凋亡率及细胞迁移能
力的改变;利用miRNA实时逆转录PCR检测细胞内let-7a表达变化。AsPC-1细胞转染let-7a mimics后,MTT法、Transwell迁
移实验分别检测细胞增殖率及细胞迁移能力的改变。结果与对照组相比,原花青素处理AsPC-1细胞后,细胞增殖率、细胞迁
移能力随着原花青素浓度升高而下降,而细胞凋亡率随着药物浓度升高而逐渐升高。与对照组相比,原花青素处理细胞后,
let-7a的表达升高。通过脂质体转染let-7a mimics后,细胞的增殖率及迁移能力均低于对照组,且let-7a mimics 与原花青素共
同作用后,细胞增殖及迁移明显低于let-7a mimics和原花青素单独作用组。结论原花青素具有抑制胰腺癌细胞生长、迁移,及
诱导细胞凋亡的作用。原花青素可能是通过上调let-7a表达,从而抑制胰腺癌细胞的生长及迁移。

Abstract: Objective To ascertain whether proanthocyanidins inhibit cell growth and migration by increasing let-7a expression
in pancreatic cancer AsPC-1 cells. Methods The proliferation rate, cell apoptosis rate and cell migration ability of AsPC-1 cells
treated with proanthocyanidins were measured by MTT assay, Annexin V-FITC/PI staining, and Transwell migration assay,
respectively. The expression of let-7a AsPC cells was detected by miRNA real-time RT-PCR after proanthocyanidins treatment.
The changes in the biological behaviors of AsPC-1 cells were evaluated after transfection with let-7a mimics. Results
Compared with the control group, proanthocyanidins treatment caused dose-dependent decrements of the proliferation rate
and migration ability and increased the apoptosis rate in AsPC-1 cells. AsPC-1 cells with proanthocyanidins treatment showed
increased expression of let-7a. Transfection with let-7a mimics resulted in obvious decreases in the cell growth rate and
migration ability, and proanthocyanidins treatment significantly enhanced the inhibitory effect of let-7a mimics. Conclusions
Proanthocyanidins-induced cell growth and migration inhibition are partially mediated by up-regulation of let-7a expression
in AsPC-1 cells.