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. 2023 Mar 20;23:258. doi: 10.1186/s12885-023-10707-7

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© The Author(s) 2023

Open AccessThis 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. 3 — TUBA1C promotes proliferation, migration, and invasion of GC cells in vitro. A CCK-8 assays were performed to test cell proliferation of MKN-45 cells and HGC-27 cells after transfection with different vectors. B EUD assays was used to detect DNA synthesis of MKN-45 cells and HGC-27 cells after transfection with different vectors. C, D Transwell assays and scratch wound healing assays to detect the invasion and migration abilities of the MKN-45 cells and HGC-27 cells after treatment. Data are mean ± SD. (Student’s t test, **P < 0.01, ***P < 0.001 )