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. 2024 Aug 8;17:161. doi: 10.1186/s13048-024-01485-2

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.

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Fig. 4 — MUC13 expression in ovarian cancer was evaluated by immunohistochemistry. A, TMA. For immunohistochemical analysis, TMA slides containing ovarian carcinoma were processed. Analysis of stromal tissue and OSE from a healthy ovary revealed no detectable MUC13 expression (a, b). MUC13 (arrows) was detected in ovarian cancer samples via membrane-bound (c) and cytoplasmic (d) staining. B, Clinical tissues. In a variety of EOC samples, the expression of MUC13 was observed. Membrane-bound (a, b) and cytoplasmic (c, d) immunostaining for MUC13 in EOC samples are depicted in the four representative panels. Magnification at the outset was 200x. (Adopted with permission from ref [84])