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RASSF4 Overexpression Inhibits the Proliferation, Invasion, EMT, and Wnt Signaling Pathway in Osteosarcoma Cells

Minglei Zhang*, Dapeng Wang, Tongtong Zhu*, Ruofeng Yin*

* Department of Orthopaedics, China–Japan Union Hospital, Jilin University, Changchun, P.R. China
† Department of Orthopaedics, Si-ping Central Hospital, Siping, P.R. China

Oncology Research 2017, 25(1), 83-91. https://doi.org/10.3727/096504016X14719078133447

Abstract

RASSF4, a member of the RASSF family, is broadly expressed in normal tissues but often inactivated in human cancers. Despite various studies on RASSF4, its role in osteosarcoma remains unclear. Therefore, in this study, we investigated the effects of RASSF4 expression on osteosarcoma cells and explored the underlying mechanism. The results of our study showed that RASSF4 was lowly expressed in osteosarcoma tissues and cells. RASSF4 overexpression significantly inhibited proliferation, migration, and invasion as well as the EMT process in osteosarcoma cells. Meanwhile, we found that RASSF4 overexpression markedly decreased the protein expression of β-catenin, cyclin D1, and c-Myc in osteosarcoma cells. In conclusion, our findings showed that RASSF4 overexpression inhibits proliferation, invasion, EMT, and Wnt signaling pathway in osteosarcoma cells. Thus, RASSF4 may be considered a novel target for osteosarcoma treatment.

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APA Style
Zhang, M., Wang, D., Zhu, T., Yin, R. (2017). RASSF4 overexpression inhibits the proliferation, invasion, EMT, and wnt signaling pathway in osteosarcoma cells. Oncology Research, 25(1), 83-91. https://doi.org/10.3727/096504016X14719078133447
Vancouver Style
Zhang M, Wang D, Zhu T, Yin R. RASSF4 overexpression inhibits the proliferation, invasion, EMT, and wnt signaling pathway in osteosarcoma cells. Oncol Res. 2017;25(1):83-91 https://doi.org/10.3727/096504016X14719078133447
IEEE Style
M. Zhang, D. Wang, T. Zhu, and R. Yin "RASSF4 Overexpression Inhibits the Proliferation, Invasion, EMT, and Wnt Signaling Pathway in Osteosarcoma Cells," Oncol. Res., vol. 25, no. 1, pp. 83-91. 2017. https://doi.org/10.3727/096504016X14719078133447



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