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. 2018 Sep 24;9(10):995. doi: 10.1038/s41419-018-1055-2

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© The Author(s) 2018

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. 5 — a Compared with the NC group, POFUT1 significantly decreased tumor size b and tumor weight c at the end of the experiment. Right panel showed representative images of SW620 xenograft tumors. Knockdown of POFUT1 in tumors from SW620-shPOFUT1 was confirmed by immunohistochemistry (IHC). d Magnification: ×10 (left, scale: 100 µm), ×40 (right, scale: 20 µm). *p < 0.05. e The metastatic lession of tumor in liver was less in shPOFUT1 groups evaluated by tail vein injection and H&E staining. Magnification: ×10 (left, scale: 100 µm), ×40 (right, scale:20 µm). *p < 0.05