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. 2023 Sep 18;14:13. doi: 10.1186/s13100-023-00300-x

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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 exploration of L1 ASP-associated genes in cancer cells. A At 48 h after transfection, the expression of LINC00491 in BHT101 cells was analyzed by RT-qPCR. B MTT assay was used to test the cell viability of BHT101 after transfection. C At 48 h after transfection, the expression of LINC00491 in OV8 cells was analyzed by RT-qPCR. D MTT assay was used to test the cell viability of OV8 after transfection. E The results of colony formation in BHT101 cells transfected with siRNA against LINC00491. F The results of colony formation in OV8 cells transfected with siRNA against LINC00491. G Transwell assay was used to test the cell migration of BHT101 after transfection. H Transwell assay was used to test the cell migration of OV8 after transfection