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. 2021 May 1;40:151. doi: 10.1186/s13046-021-01957-z

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© The Author(s) 2021

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. 3 — Lnc-CTSLP8 promoted autophagy in ovarian cancer cells. a GSEA analysis of SKOV3-CTSLP8-OE and SKOV3-CTSLP8-NC (control vector). The signature was defined by genes with significant expression changes. b Transmission electron microscopy (TEM) was used to observe autophagosomes (AU), autolysosomes (AL), and mitochondria (MT) in different cell lines. c Immunoblotting of autophagy-related genes in different cell lines. d Quantification of immunoblotting analysis revealed the relative SQSTM1-p62 expression and LC3-II/ LC3-I ratio in different cell lines (Student t-test). e Immunofluorescence assay of mRFP-GFP-LC3 in different cell lines