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. 2022 Jul 11;13(7):597. doi: 10.1038/s41419-022-05040-z

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© The Author(s) 2022

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. 4 — Rescue assays were performed in SK-N-AS and SK-N-SH cells transfected with sh-NC, sh-SNHG25#1, and sh-SNHG25#1+lenti-SNORA50C, respectively. A–C CCK-8 assay, colony formation assay, and flow cytometry analysis detected the proliferation and apoptosis of SK-N-AS and SK-N-SH cells. D–F Transwell and wound healing assays detected the invasion and migration of SK-N-AS and SK-N-SH cells. One-way ANOVA, Tukey. ^**P < 0.01. Error bars indicate mean ± SD. (N = 3).