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. 2022 May 19;8:266. doi: 10.1038/s41420-022-01036-y

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© The Author(s) 2022

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. 6 — A, B The NEAT1 (A) and miR-342 (B) expression levels in LX-2 cells were assessed via qRT-PCR. C The LX-2 cell proliferation was examined by the CCK-8 assay. D The cell cycle of the LX-2 was examined by the flow cytometry. E, F The migration of LX-2 was determined by the scratch assay (E) and the transwell assay (F). G The protein levels of collagen I, α-SMA, fibronectin, Sp1, TGF-β1, p-Smad2, Smad2, p-Smad3 and Smad3 were measured by western blot. *p < 0.05; **p < 0.01; ***p < 0.001.