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. 2018 Apr 27;9(5):465. doi: 10.1038/s41419-018-0497-x

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© The Author(s) 2018

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. 7 — NCI-H1975 cells were infected with HOXA4 overexpression lentivirus or control vector lentivirus (Vector). LiCl (20 mM) was added at 24 h post viral infection. CCK-8 (a) and transwell assays (b) were performed to determine the proliferation, invasion and migration abilities of NCI-H1975 cells with LiCl treatment and HOXA4 overexpression. ***P < 0.001 vs. Vector; ^###P < 0.001 vs. HOXA4; ⁺⁺P < 0.01 and ⁺⁺⁺P < 0.001 vs. Vector+LiCl