ING4 Inhibits Proliferation and Induces Apoptosis in Human Melanoma A375 Cells via the Fas/Caspase-8 Apoptosis Pathway

被引:11
|
作者
Ma, Yanli [1 ]
Cheng, Xue [1 ]
Wang, Fei [1 ]
Pan, Jisheng [1 ]
Liu, Jing [1 ]
Chen, Hongxiao [3 ]
Wang, Yongchen [2 ]
Cai, Limin [1 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 1, Dept Dermatol, 23 Youzheng St, Harbin 150001, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 2, Dept Dermatol, 246 Xue Fu Lu, Harbin 150081, Peoples R China
[3] Chinese Peoples Liberat Army 404st Hosp, Dept Dermatol, Weihai, Peoples R China
基金
中国国家自然科学基金;
关键词
Apoptosis; Fas/caspase-8; apoptosis; Inhibitor of growth 4; Malignant melanoma; Proliferation; TUMOR-SUPPRESSOR GENE; DOWN-REGULATION; GROWTH; 4; EXPRESSION; INVASION; FAMILY;
D O I
10.1159/000444050
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Inhibitor of growth 4 (ING4) plays a role in regulating the cell cycle, apoptosis, cell invasion and migration, but the mechanisms involved remain to be elucidated. Objective: To explore how ING4 affects human malignant melanoma A375 cells. Methods: Recombinant lentiviral vectors (A375/pLenO-GTP-ING4) were constructed and transfected into A375 cells (experimental group). The impact of ING4 on the proliferation and apoptosis of A375 cells was investigated in in vitro and in vivo experiments in mice using the MTT assay and flow cytometry. Results: In the experimental group, optical density was lower and apoptotic cells were more frequent from days 2-5 (p = 0.000 and p < 0.01); there were smaller xenografts and more apoptotic cells in mice (all p < 0.05); moreover, increased levels of Fas, cleaved caspase-8 and caspase-3, and decreased levels of FasL and procyclic acidic repetitive protein were observed in vitro and in vivo. Conclusion: ING4 might suppress proliferation and enhance apoptosis in human malignant melanoma cells by activating Fas-induced apoptosis in a caspase-8-dependent pathway. (C) 2016 S. Karger AG, Basel
引用
收藏
页码:265 / 272
页数:8
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