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. 2020 Jul 2;11(7):509. doi: 10.1038/s41419-020-2699-2

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© The Author(s) 2020

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. 2 — a qRT-PCR analysis of SPEN after SPEN silencing by siRNAs. *P < 0.05. b Expression levels of p-PI3K, PI3K, p-AKT, AKT, and c-JUN were determined in HONE1 and 5–8F cell lines by western blot after transfection of siRNAs for SPEN. Slience d SPEN significantly inhibited HONE1 and 5-8 F cell migration and invasion as examined by transwell and boyden assays (c) and wound-healing assay (d), respectively. Data are presented as mean ± SD for three independent experiments. *P < 0.05.