GSK-3 inhibitor inhibits cell proliferation and induces apoptosis in human osteosarcoma cells

被引:21
作者
Nishimura, Hideki [1 ]
Nakamura, Osamu [1 ]
Yamagami, Yoshiki [1 ]
Mori, Masaki [1 ]
Horie, Ryosuke [1 ]
Fukuoka, Natsuko [1 ]
Yamamoto, Tetsuji [1 ]
机构
[1] Kagawa Univ, Dept Orthopaed Surg, Fac Med, 1750-1 Ikenobe, Miki, Kagawa 7610793, Japan
关键词
glycogen synthase kinase-3; SB216763; apoptosis; osteosarcoma; GLYCOGEN-SYNTHASE KINASE-3-BETA; FACTOR-KAPPA-B; PANCREATIC-CANCER; GENE-TRANSCRIPTION; KINASE-ACTIVITY; CYTOCHROME-C; SURVIVAL; PROTEIN; TARGET; TUMORIGENESIS;
D O I
10.3892/or.2016.4565
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glycogen synthase kinase-3 (GSK-3) is a serine/threonine kinase that functions in numerous signaling pathways initiated by diverse stimuli. The functions of GSK-3 in cancer differ depending on cell type. In the present study, we examined the effects of a specific GSK-3 inhibitor on the regulation of osteosarcoma cell proliferation and apoptosis. Immunohistochemical analysis and real-time reverse transcription-polymerase chain reaction (RT-PCR) were performed to determine the expression pattern of GSK-3 in human osteosarcoma cells. We used the MTS assay, western blotting, measurement of single-stranded DNA and morphological analyses to study the effects of a GSK-3 inhibitor, SB216763 on osteosarcoma cell proliferation and survival. We detected an increase in mRNA expression of GSK-3 and aberrant nuclear accumulation of GSK-3 in the osteosarcoma cells. Pharmacological inhibition of GSK-3 led to a decrease in proliferation and survival of osteosarcoma cells. Inhibition of GSK-3 resulted in a decreased expression of Bcl-2 and a subsequent increase in osteosarcoma cell apoptosis via the mitochondrial pathway. The present study demonstrated that GSK-3 activity is critical for tumorigenicity and cell survival in osteosarcoma cells. Our findings suggest that GSK-3 is a potential therapeutic target for the treatment of human osteosarcoma.
引用
收藏
页码:2348 / 2354
页数:7
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