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. 2022 Jan 10;17:4. doi: 10.1186/s13062-021-00314-6

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© The Author(s) 2022

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 — LINC00885 was upregulated in CC and predicted poor prognosis. A Bioinformatics tool (GEPIA) was applied for analyzing the expressions of LINC00885 in CESC tissues and normal tissues. B RT-qPCR was done for the analysis of LINC00885 expression in four CC cell lines (SiHa, CaSki, C33a, and HeLa) and cervical epithelial immortalized cell line (H8). C RT-qPCR was done for the measurement of LINC00885 expression in 80 CC samples and the matched para-cancerous samples. D Kaplan–Meier analysis and log-rank test confirmed the prognostic significance of LINC00885 expression in CC patients. ^*P < 0.05, ^**P < 0.01, ^***P < 0.001