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. 2018 Feb 14;9(2):220. doi: 10.1038/s41419-018-0295-5

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — a–c NB-EBC1 cell growth (a and c) and cell death (b) upon indicated treatment were determined by live-cell imaging analysis (IncuCyte ZOOM™) (right panel). The cell confluences or death percentage of control group were set to 100% or 1 in the bar graph (left panel), respectively. Error bars represent standard deviation from the mean of quadruplicate samples. d, e Tumor xenograft was established by using NB975A2 cells and mice were treated daily with 300 mg/kg DMF or vehicle controls. The tumor volumes of control group and DMF-treated group were monitored daily. The tumor volumes of vehicle control group were set to 100%. Error bars represent SEM from the mean of 10 tumors. Data are representative of three independent experiments