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. 2017 Sep 6;7:10718. doi: 10.1038/s41598-017-11417-4

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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 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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GE triggered ER stress and activated IRE-1α pathway in HEY and A2780 cells. (A) The related proteins were examined by western blot. After transiently transfected with scramble or IRE-1α siRNA and treated with GE for 24 h, the cells were examined by annexin V/PI staining assay (B), and the proteins were examined by western blot (C). The full-length gels of western blot were shown in the Supplementary Information file. All experiments were performed at least three times.