Molecular mechanism underlying the inhibitory effect of spermine oxidase inhibitor SI-4650 on proliferation of a human malignant melanoma cell line A375
- VernacularTitle: 精胺氧化酶抑制剂SI-4650抑制人恶性黑素瘤A375细胞增殖的分子机制研究
- Author:
You ZHOU
1
;
Yanlin WANG
;
Chunyu CAO
;
Lidan SUN
;
Jianlin YANG
Author Information
- Publication Type:Journal Article
- Keywords: Melanoma; Spermine; Spermidine; Cell proliferation; Apoptosis; Autophagy; Cell line, tumor; Spermine oxidase inhibitor
- From: Chinese Journal of Dermatology 2019;52(10):722-728
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To evaluate the effect of spermine oxidase (SMO) inhibitor SI-4650 on the proliferation of a human malignant melanoma cell line A375, and to explore its molecular mechanism.
Methods:Some cultured A375 cells were divided into 6 groups to be treated with SI-4650 at concentrations of 0, 10, 20, 40, 80 and 160 μmol/L respectively for 24, 48 and 72 hours, and methyl thiazolyl tetrazolium (MTT) assay was performed to evaluate changes in cellular proliferative activity. According to the cellular proliferative activity, 3 concentrations (0, 40, 80 μmol/L) were screened out. Some A375 cells were divided into 3 groups to be treated with 0 (control group) , 40 and 80 μmol/L SI-4650 for 48 hours. Chemiluminescence assay was conducted to detect the SMO activity in A375 cells, high-performance liquid chromatography (HPLC) analysis to determine the polyamine content in A375 cells, flow cytometry to analyze the cell cycle and detect the apoptosis, and Western blot analysis to determine the protein expression of apoptotic marker proteins Bax and c-PARP, inhibitor of apoptosis protein Bcl-2, and autophagy marker proteins Beclin-1 and LC3-Ⅱ. Statistical analysis was carried out by using one-way analysis of variance for comparison of means among several groups, and by using Student-Newman-Keuls (SNK) -q test for multiple comparisons.
Results:MTT assay showed that there was a significant difference in the proliferative activity of A375 cells after the treatment with different concentrations of SI-4650 for different durations (F = 977.23, 5.16 respectively, bothP < 0.001) . Significant differences were observed in the SMO activity in A375 cells (F = 242.58,P < 0.001) , spermine and the total polyamine content (F = 338.02, 2 931.07 respectively, bothP < 0.001) , proportion of S-phase cells (F = 31.66,P < 0.001) , proportion of apoptotic cells (F = 100.68,P < 0.001) , expression of apoptosis-related proteins Bax, c-PARP and Bcl-2 (F = 35.51, 730.11, 27.54 respectively, allP < 0.001) , and expression of autophagy marker proteins Beclin-1 and LC3-Ⅱ (F = 35.87, 425.04 respectively,P < 0.001) among the control group, 40- and 80-μmol/L SI-4650 groups. Compared with the control group, the 40- and 80-μmol/L SI-4650 groups showed significantly lower SMO activity (luminous intensity: 61 432.85 ± 2 620.92, 43 337.35 ± 1 221.25 respectively, bothP < 0.05) , lower spermine (1.97 ± 0.007, 1.88 ± 0.006 respectively, bothP < 0.05) and total polyamine content (3.18 ± 0.03, 2.81 ± 0.01 respectively, bothP < 0.05) , higher proportions of S-phase cells (27.61% ± 2.05%, 31.58% ± 1.45% respectively, bothP < 0.05) and apoptotic cells (27.61% ± 2.05%, 31.58% ± 1.45% respectively, bothP < 0.05) , higher expression of apoptotic marker proteins Bax (0.83 ± 0.12, 1.18 ± 0.16 respectively, bothP < 0.05) and c-PARP (0.32 ± 0.002, 0.79 ± 0.035 respectively, bothP < 0.05) and autophagy marker proteins Beclin-1 (1.00 ± 0.007, 1.14 ± 0.003 respectively, bothP < 0.05) and LC3-Ⅱ (0.31 ± 0.001, 0.98 ± 0.003 respectively, bothP < 0.05) , and lower expression of inhibitor of apoptosis protein Bcl-2 (0.65 ± 0.09, 0.12 ± 0.002 respectively, bothP < 0.05) .
Conclusion:SI-4650 can inhibit the proliferation of A375 cells, likely by interfering with polyamine metabolism and inducing cell cycle arrest, apoptosis and autophagy.
