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. 2021 Jan 5;34(2):588–597. doi: 10.1007/s13577-020-00470-3

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© The Author(s) 2021

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/.

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Fig. 6 — MAFG-AS1 promoted BC cell proliferation, migration, and invasion by regulating miR-125b-5p/SphK1 axis. HT-1197 cells were transfected with MAFG-AS1 expression vector, SphK1 expression vector or miR-125b-5p mimic. Cell proliferation was detected by CCK-8 assay (a). Cell invasion was detected by Transwell invasion assay (b). Cell migration was detected by wound healing assay (c). All experiments were repeated 3 times and mean values were presented. *, p < 0.05