Abstract
Triple-negative breast cancer (TNBC) is an aggressive subtype of breast cancer with limited effective treatment options. New therapeutic approaches are urgently needed to improve the prognosis of TNBC. Here we demonstrated that a redox modulator, selenocystine (SeC), significantly inhibits TNBC cell proliferation in a dose- and time-dependent manner. Through cell apoptosis assays and cell cycle distribution analyses, we have shown that the in vitro inhibitory effect of SeC on TNBC cells can be attributed to the induction of apoptosis and the S-phase arrest in a dose-dependent manner. Therefore, this finding implies that SeC potentially is a novel therapeutic agent for TNBC.
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Acknowledgments
We thank Prof. Musheng Zeng for providing the human TNBC cell lines and Prof. Tianfeng Chen for providing the SeC. This research was supported by the Female Tumor Drugs Research Foundation of Guangdong Pharmaceutical Association (No. 2014D09).
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Editor: Tetsuji Okamoto
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Long, M., Wu, J., Hao, J. et al. Selenocystine-induced cell apoptosis and S-phase arrest inhibit human triple-negative breast cancer cell proliferation. In Vitro Cell.Dev.Biol.-Animal 51, 1077–1084 (2015). https://doi.org/10.1007/s11626-015-9937-4
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DOI: https://doi.org/10.1007/s11626-015-9937-4