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. 2018 May 9;9:487. doi: 10.3389/fphar.2018.00487

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Copyright © 2018 Zhang, Wang, Wang, Sun, Du, Ye, Sun and Sun.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Effects of Sal A and ATO treatment on the cell viability of cancer cells. SGC7901, HepaRG, K562 and HL60 cells were treated with ATO (5 μM) in the presence or absence of Sal A (25 μM) for 24 h. Cell viability was determined by the CCK8 assay and expressed as a percentage of the control for each cell line. The data are expressed as the means ± SD of three independent experiments. ^##p < 0.01 versus control; ^##p < 0.01 versus control; ^∗p < 0.05 versus ATO-treated cells; ^∗∗p < 0.01 versus ATO-treated cells.