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. 2021 Sep 17;14:121. doi: 10.1186/s13048-021-00877-y

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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. 1 — UBE2S is correlated with poor prognosis in HGSOC. A qRT-PCR was performed to detect the mRNA levels of UBE2S in normal fallopian tube (FT) and high-grade serous ovarian carcinoma (HGSOC) tissues. B Western blot analysis of the protein levels of UBE2S and β-actin in FT and HGSOC (T) tissues. C Quantification of relative protein levels of UBE2S in (B). D Representative images of IHC staining of UBE2S in HGSOC and FT tissues (Upper, 40×; Lower, 400×). E Overall survival (OS) analysis based on UBE2S expression in HGSOC patients. (Data are mean ± SEM, **p < 0.01)