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. 2020 May 6;20:152. doi: 10.1186/s12935-020-01223-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. 1 — FENDRR inhibits cervical cancer progression in vitro and vivo. a, b qRT-PCR analysis of relative FENDRR expression in CC tissues and cells. c FENDRR overexpression efficiency. d–f CCK-8, colony formation assay and flow cytometry assay to detect cell viability, proliferation and apoptosis after overexpressing FENDRR. g Transwell assays to detect cell migration and invasion after overexpressing FENDRR. h Western blot assay examined EMT process after FENDRR overexpression. i In vivo experiments demonstrated FENDRR oncogenic role. **p < 0.01