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. 2018 Jan 26;9(2):129. doi: 10.1038/s41419-017-0120-6

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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. 5 — a Relative tumor volumes, b tumor weights, and c body weights were measured in PC9/ER xenografts treated with UNC0642, Erlotinib or the combination of UNC0642 and Erlotinib. d H3K9Me2, PTEN, p-AKT, and AKT expression levels were measured in PC9/ER xenograft tumor tissues. β-actin was used as a loading control. *P < 0.05, **P < 0.01, compared to control; ^#P < 0.05, combined treatment group compared to UNC0642 single treatment group