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. 2022 Jan 12;20:7. doi: 10.1186/s12964-021-00760-9

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© The Author(s) 2022

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 8 — Inhibiting PI3K-Akt pathway in glioblastoma-derived EVs-treated mNPCs reversed elevated NPC migration. A Wortamnnin significantly reversed U87-EVs-elevated migration cell numbers in U87-EVs-treated mNPCs in the transwell assay. B Wortamnnin significantly reversed U87-EVs-elevated relative width of scratch in U87-EVs-treated mNPCs in wound healing assay. Results are presented as the mean ± SD of three independent experiments. *p < 0.05, ***p < 0.001. Scale bar, 100 μm (A) and 200 μm (B)