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. 2023 Jul 13;23:136. doi: 10.1186/s12935-023-02978-8

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© The Author(s) 2023

Open Access This 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 — snoRNAs: SNORD15A, SNORD35B and SNORD60 as non-invasive diagnostic biomarkers for RCC. (A): Stability of snoRNAs in US: there was no statistical difference in the expression of SNORD15A, SNORD35B and SNORD60 between the control group (without RNase treatment) and the RNase group (with RNase treatment). (B): SNORD15A, SNORD35B and SNORD60 were up-regulated in US of RCC patients (n = 100) compared with healthy controls (n = 131); (C): ROC curve analysis of SNORD15A, SNORD35B and SNORD60 and their combination for RCC diagnosis. ****P < 0.0001; NS, no significance