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. 2021 May 31;21:287. doi: 10.1186/s12935-021-01991-z

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© The Author(s) 2021

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. 2 — GOLT1B promotes CRC cell proliferation, invasion and migration. a, b GOLT1B mRNA and protein level were determined by qPCR and western blot in HCT116 and RKO cells. c, d Cell migration were determined by wound healing experiment after siRNA transfection or overexpression of GOLT1B, respectively. e, f Cell invasion were detected by transwell assays with matrigel after siRNA transfection or overexpression of GOLT1B, respectively. g Effect of GOLT1B on proliferation of colorectal cancer cells in vitro. All data are shown as mean ± S.E.M. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001