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. 2020 Sep 11;11(9):741. doi: 10.1038/s41419-020-02967-z

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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. 6 — LIN28B-AS1 KO (“KO-LIN28B-AS1”) or the control (“CRISPR-C”) HepG2 cells were inoculated s.c. to the flanks of the nude mice; Tumor volumes a and mice body weights c were recorded every 7 days for a total of 42 days. Daily tumor growth was calculated as described b; At Day-14, three HepG2 tumors of each group were isolated, expression of LIN28B-AS1 and listed genes were shown d–f. Bars stand for mean ± standard deviation (SD). *p < 0.05 vs. “CRISPR-C” tumors.