The mechanism of cordycepin in inhibition of pancreatic cancer stem cells proliferation and metastasis
10.16438/j.0513-4870.2017-0353
- VernacularTitle:虫草素抑制胰腺癌干细胞增殖及转移的机制研究
- Author:
Jian-bing LIU
1
;
Meng QI
1
;
Qiao-qi LI
1
;
Jia-huan LI
1
;
Kai-hui HU
1
;
Wen-xiong LIN
1
;
Jun-sheng FU
1
Author Information
1. College of Life Sciences, Fujian Agriculture and Forestry University, Fuzhou 350002, China
- Publication Type:ORIGINAL ARTICLES
- Keywords:
cordycepin;
pancreatic cancer stem cell;
cellular apoptosis;
epithelial-mesenchymal transition;
proliferation;
metastasis
- From:
Acta Pharmaceutica Sinica
2017;52(9):1404-1409
- CountryChina
- Language:Chinese
-
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.
