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. 2021 Jul 7;21:784. doi: 10.1186/s12885-021-08344-z

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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/. 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. 3 — Functional experiment of MCM6 in neuroblastoma cells. (A) Western blotting verified the protein expression of MCM6 in 5 neuroblastoma cell lines; (B) Interference efficiency of 3 small interfering RNAs with different sequences on MCM6, detected by qRT-PCR; The in vitro proliferation function of MCM6 was measured by CCK-8 (C), colony formation (D) and flow cytometry EdU labeling detection (E). The wound healing experiment (F) and the Transwell migration and invasion experiment (G-H) verified the migration (G) and invasion (H) activities of MCM6 on neuroblastoma cells in vitro. EdU, 5-Ethynyl − 2′- deoxyuridine