Inhibition of Aurora-B suppresses osteosarcoma cell migration and invasion
Author(s) -
Xiao Ping Zhu,
Zhili Liu,
Ai Peng,
Yun Zhou,
Xin Long,
Qing Luo,
Shan Huang,
Yong Shu
Publication year - 2014
Publication title -
experimental and therapeutic medicine
Language(s) - English
Resource type - Journals
eISSN - 1792-1015
pISSN - 1792-0981
DOI - 10.3892/etm.2014.1491
Subject(s) - aurora b kinase , metastasis , cell cycle , cancer research , osteosarcoma , oncogene , immunohistochemistry , cell growth , cell migration , aurora inhibitor , cell , biology , cell culture , apoptosis , cancer , pathology , medicine , cell division , cytokinesis , biochemistry , genetics
Previous studies have suggested that Aurora-B may be involved in cancer metastasis. However, its role has been poorly evaluated in osteosarcoma (OS). The aim of this study was to investigate the correlation between Aurora-B expression and metastasis in human OS. The human OS cell line, U2-OS, and OS biopsy specimens were used in the study. The expression of Aurora-B protein was examined using immunohistochemistry and western blotting in OS tissues and U2-OS cells, respectively. AZD1152-hydroxyquinazoline-pyrazol-anilide, an inhibitor of Aurora-B, was used to inhibit Aurora-B expression in U2-OS cells. The effect of Aurora-B inhibition on U2-OS cell proliferation, invasion and migration was assessed using MTT, colony formation, wound healing and Transwell assays. The results showed that positive expression of the Aurora-B protein was observed in the nucleus, and that Aurora-B expression levels in the cases with pulmonary metastases were significantly higher than in those without metastasis. In vitro , the proliferation, invasion and migration of U2-OS cells were suppressed by the inhibition of Aurora-B. These results suggest that Aurora-B may be involved in OS metastasis, and may be a promising target in the treatment of OS metastasis.
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