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. 2023 Feb 16;23:160. doi: 10.1186/s12885-023-10639-2

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© The Author(s) 2023

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/. 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. 8 — Functional experiments against LINC02154 in ACHN cells. A Relative expression levels of LINC02154 after transfection with the corresponding siRNA. B CCK-8 assay was used to detect the effect of LINC02154 on ACHN cell proliferation. C The effect of LINC02154 on ACHN cell proliferation was examined by EdU assay. D Wound-healing assay was used to test the effect of LINC02154 on ACHN cell migration. E The Transwell assay was used to test the effect of LINC02154 on ACHN cell migration. F Western blot indicated that FDX1 and DLST were significantly upregulated in the LINC02154-Si group relative to the LINC02154-NC group