Effect of salinomycin on proliferation and autophagic flow of human malignant melanoma M21 cells
10.11904/j.issn.1002-3070.2018.03.002
- VernacularTitle:盐霉素对人黑色素瘤M21细胞增殖及自噬流的影响
- Author:
Yajing LIU
1
;
Guoyu LIU
;
Shubin WANG
;
Zhengyu FANG
Author Information
1. 深圳北京大学香港科技大学医学中心 深圳 518036
- Keywords:
Malignant melanoma;
M21 cell line;
Salinomycin;
Autophagy
- From:
Practical Oncology Journal
2018;32(3):203-207
- CountryChina
- Language:Chinese
-
Abstract:
Objective The objective of this study was to investigate the effect of salinomycin on proliferation and autophagic flux of human melanoma M21 cells. Methods The cell survival rate was determined by MTS assay and IC50values( half inhibitory concentration)were calculated. The morphological changes of cells after salinomycin administration were observed under optical micro-scope. Flow cytometry was used to examine the apoptosis rate of M21 cells. Western blot was used to detect the expression of autophag-ic-related protein LC3B and p62 in M21 cells. The presence of autophagosomes in M21 cells after salinomycin administration was ob-served under transmission electron microscope. Western blot and immunofluorescence were used to detect the level of p62 protein and localizing changes in M21 cells. Results Salinomycin significantly inhibited proliferation of M21 cells, and the IC50values were (1. 38 ± 0. 18)μM. After salinomycin administration,the proliferation rate of M21 cells was slowed down,and obvious vacuoles ap-peared in the cells. Salinomycin could not only induce cell apoptosis,but it also increased the ratio of LC3B-Ⅱ/LC3B-Ⅰ in M21 cells. The increase and accumulation of autophagosomes were directly observed under transmission electron microscope. The level of p62 protein was slightly elevated after salinomycin treatment and gradually aggregated into the cytoplasm,indicating that autophagic flux was inhibited. Conclusion Salinomycin can inhibit the proliferation of human malignant melanoma M21 cells,and its mechanism may be related to the accumulation autophagosomes granules and inhibition of autophagic flux.
