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. 2021 Apr 27;11:9016. doi: 10.1038/s41598-021-88512-0

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© The Author(s) 2021

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 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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Nek2 is required for invasion and migration in triple-negative breast cancer cells. (a–d) Invasion and migration of MDA-MB-231 cells treated with siNek2 (a) and (b) or INH6 (c) and (d). (e–f) Invasion and migration of Hs578t treated with siNek2. (g,h) CCK8 cell proliferation assay was assessed in MDA-MB-231 using siNek2 (g) or INH6 (h). Data represent mean fold change ± SEM of three independent experiments.

Nek2 is required for invasion and migration in triple-negative breast cancer cells. (a–d) Invasion and migration of MDA-MB-231 cells treated with siNek2 (a) and (b) or INH6 (c) and (d). (e–f) Invasion and migration of Hs578t treated with siNek2. (g,h) CCK8 cell proliferation assay was assessed in MDA-MB-231 using siNek2 (g) or INH6 (h). Data represent mean fold change ± SEM of three independent experiments.