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. 2020 May 18;123(3):426–437. doi: 10.1038/s41416-020-0884-9

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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. 5 — Cell migration ability was determined in MDA-MB-231/miR-622 cells by wound healing (a) and by Transwell migration (b) assays. c Wound healing was also performed in MDA-MB-231 transfected with Anti-miR-622 respect to control cells (Anti-miR-Null). d Expression level of miR-622 was monitored, by q-RT-PCR, in MCF-7 cell line after stable transfection with miR-622 (left) or with Anti-miR-622 (right) plasmids respect to relative control cells (MCF-7/miR-Null or MCF7/Anti-miR-Null). e Cell migration ability was determined by Transwell migration assay also in MCF-7 after stable transfection. Data are presented as the mean ± S.D. *p < 0.05; **p < 0.01; ***p < 0.001.