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. 2020 Dec 11;39:280. doi: 10.1186/s13046-020-01790-w

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© The Author(s). 2020

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 — Silencing of hsa_circ_0001829 inhibits GC cells proliferation, migration and invasion in vitro. a The interference efficiency of three hsa_circ_0001829-targeting siRNAs on hsa_circ_0001829 and SLC45A4 mRNA level were examined by qRT-PCR. b-c CCK-8 and EdU assays of GES-1-T and MKN-28 cells transfected with control or siRNAs. d Colony formation assay of GES-1-T and MKN-28 cells stably transfected with control or shRNAs by lentiviral infection. e-f Transwell and wound healing assays of GES-1-T and MKN-28 cells transfected with control or siRNAs. *p < 0.05, ** p < 0.01