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. 2017 Nov 27;6(11):396. doi: 10.1038/s41389-017-0002-x

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© The Author(s) 2017

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 articles Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the articles 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. 4 — a BCK4 cells were placed in phenol red free media with steroid depleted serum 24 h prior to treatment with vehicle (EtOH), estradiol (E2), fulvestrant (ICI), imatinib mesylate (Imat) or combined treatments as specified. Proliferation was measured using the IncuCyte live cell imaging system. Fold change was calculated vs. time zero. b MDA-MB-134VI (MM134) or c SUM44PE (SUM44) cells were plated as specified above for 24 h prior to treatment with vehicle (EtOH), estradiol (E2), imatinib mesylate (Imat) or the combination of E2+Imat as specified. Proliferation was measured using the IncuCyte live cell imaging system for the times specified. Error bars show SEM. Asterisk indicates p < 0.0001 vs. vehicle control using two way ANOVA