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. 2021 Jun 29;54:18. doi: 10.1186/s40659-021-00340-8

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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 — The interrelation of m5C-associated molecular subtypes and clinicopathological characteristics in patients with ovarian cancer. A The death rate of the C1 subgroup with poor prognosis was higher. B–D There was no significant difference in stage, grade and age between the two subtypes. E, F C1 was significantly higher than C2 in memory B cell and eosinophil immune-related cells, and lower than C2 in activated CD4 T cell, activated CD8 T cell, type 1 T helper cell, type 2 T helper cell and CD56dim natural killer cell. G the expression of 13 M5C related genes in the two subtypes