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. 2022 Oct 12;12:999654. doi: 10.3389/fonc.2022.999654

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Copyright © 2022 Li, Liu, Chen, Zhang, Wu and Wang

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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The immune-related prognostic signature was established and validated in TCGA-RNA-Seq cohort and HG-U133_Plus_2 cohort, respectively. Distributions of risk scores and survival status of OC patients in the TCGA-RNA-Seq cohort (A) and HG-U133_Plus_2 cohort (D); Heat map analysis showed the association between risk score and the expression of the five lncRNAs in TCGA-RNA-Seq cohort (B) and HG-U133_Plus_2 cohort (E); Kaplan–Meier curves showed that the high-risk subgroup had worse OS than the low-risk subgroup in TCGA-RNA-Seq cohort (C) and HG-U133_Plus_2 cohort (F). ROC curves of the immune-related lncRNAs for predicting 5-year survival in TCGA-RNA-Seq cohort (G) and HG-U133_Plus_2 cohort (H).