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. 2020 Oct 23;11(10):908. doi: 10.1038/s41419-020-03095-4

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© The Author(s) 2020

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. 4 — (A) LUCAT1-KO HCT116 and SW620 cells were transfected with the indicated shRNAs, and MYC expression was quantified by qRT-PCR. GAPDH was used as a control. (B) LUCAT1-KO HCT116 and SW620 cells were transfected with the indicated shRNAs, and MYC expression was quantified by a Western blot. GAPDH was used as a control. (C) LUCAT1-KO HCT116 and SW620 cells were transfected with the indicated shRNAs, and the proliferation ability was quantified by a CCK8 assay. (D) LUCAT1-KO HCT116 and SW620 cells were transfected with the indicated shRNAs, and the colony formation ability was quantified by a colony formation assay. The results are presented as the mean ± s.d. and are representative of at least three independent experiments. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.