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. 2018 Jul 3;9(7):746. doi: 10.1038/s41419-018-0768-6

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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. 2 — a qRT-PCR detected the expression of SNHG1 after siRNA transfection in HuCCT1 and RBE cell lines. b Colony formation assays were used to determine the cell colony formation ability of si-SNHG1-transfected cells. c CCK8 assays were used to determine the cell viability of si-SNHG1-transfected cholangiocarcinoma cells. d Transwell assays showed that SNHG1 knockdown inhibited cholangiocarcinoma cell migration.Error bars indicate means ± SD. *P < 0.05; **P < 0.01;***P < 0.001;****P < 0.0001.