Inhibition of luteoloside on proliferation of human esophageal carcinoma cell line Eca109 and its mechanism
10.7501/j.issn.0253-2670.2013.12.016
- Author:
Ting-Ting WANG
1
Author Information
1. School of Public Health
- Publication Type:Journal Article
- Keywords:
Cell apoptosis;
Cell cycle;
Cell growth;
Esophageal cancer cell line Eca109;
Gene expression;
Luteoloside
- From:
Chinese Traditional and Herbal Drugs
2013;44(12):1604-1609
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To investigate the inhibition of luteoloside on the proliferation of human esophageal carcinoma cell line Eca109 and its mechanism. Methods: MTT assay was used for detecting the influence of luteoloside at different concentration on the proliferation of Eca109. The morphological changes of cells were observed under inverted microscope. The cell cycle and apoptosis were detected by flow cytometry. RT-PCR was used to detect the mRNA expression of cyclin D1, survivin, and c-myc genes. Results: The results of MTT assay showed different doses (80, 120, 160, 200, and 240 μmol/L) of luteoloside could inhibit the cell proliferation of Eca109 cells in a dose-response manner. Luteoloside could also change the morphological characteristics of cells, reduce the cell size, and separate from peripheral cells. Treated with 240 μmol/L luteoloside, the cells were sprouting and some of them developed multiple pseudopodia-like protrusions. Treated with luteoloside (160 and 240 μmol/L), the cell cycle of Eca109 cells was blocked in G2/M phase and apoptosis was induced (P < 0.05). Compared with the control group, the gene expression of cyclin D1, survivin, and c-myc was decreased after treated with 240 μmol/L luteoloside for 48 h (P < 0.05). Conclusion: Luteoloside could significantly inhibit the proliferation of Eca109 cells by changing the cell cycle and inducing the apoptosis. Moreover, it could decrease the mRNA expression of relative genes.
