Back to Search Start Over

硫酸右旋糖苷对人胃癌MGC-803细胞增殖和凋亡的影响.

Authors :
王文莙
曹相玫
马艳梅
杨媛媛
徐远义
黄允宁
Source :
Tianjin Medical Journal. Jun2019, Vol. 47 Issue 6, p605-609. 5p.
Publication Year :
2019

Abstract

Objective To investigate the effect of dextran sulfate (DS) on the proliferation and apoptosis in human gastric cancer MGC-803 cells and its mechanisms. Methods Human gastric cancer MGC-803 cells were cultured and divided into control group (PBS group) and experimental group (DS group). The effect of DS on the proliferation of gastric cancer MGC-803 cells was detected by EdU cell proliferation assay. Plate colony formation assay was used to detect the effect of DS on colony forming ability of MGC-803 cells. Changes of the apoptosis were determined by AnnexinV-PI double staining. Western blot assay was also used to analyze the protein expression levels of EZH2, Cleaved-caspase3 at different time points (2 h, 8 h, 12 h and 24 h). Results EdU results showed that DS significantly inhibited the proliferation of gastric cancer MGC-803 cells compared with that of the control group (P<0.01). The plate colony formation experiment showed that cell colony forming ability was significantly decreased in experimental group than that of the control group (P<0.01). The result of AnnexinV-PI double staining showed that the apoptosis rate was significantly higher in the experimental group than that of the control group (P<0.01). Western blot analysis showed that after DS intervention the protein expression of EZH2 was significantly decreased in MGC-803 cells compared with that of control (P<0.05), and the protein expression level of Cleaved-caspase3 was significantly increased (P<0.05). Conclusion DS can significantly inhibit the proliferation and induce apoptosis of human gastric cancer MGC-803 cells, which may be related to the inhibition of EZH2 expression. [ABSTRACT FROM AUTHOR]

Details

Language :
Chinese
ISSN :
02539896
Volume :
47
Issue :
6
Database :
Academic Search Index
Journal :
Tianjin Medical Journal
Publication Type :
Academic Journal
Accession number :
143345681
Full Text :
https://doi.org/10.11958/20181795