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. 2019 Jun 6;10(6):448. doi: 10.1038/s41419-019-1671-5

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© The Author(s) 2019

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 The Boyden assay revealed that glioma cell invasion ability was decreased in the LV-miR-708 group. b The in vivo assay revealed that miR-708 decreased the number and size of metastatic pulmonary nodules. c The formation of stress fiber in glioma cells was decreased in the LV-miR-708 group. d The epithelial marker E-cadherin was increased, whereas expression of the mesenchymal markers N-cadherin and vimentin were decreased in the LV-miR-708 group, as determined by western blot assay