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. 2022 Jan 25;20:50. doi: 10.1186/s12951-022-01264-5

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© The Author(s) 2022

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. 7 — miR497/TP-HENPs induced ROS production in cisplatin-resistant OC and regulated macrophage polarization from M2 to M1 in vivo. A The ROS of tumor sections after treatments. Scale bar: 50 µm. B, C Serum levels of TNF-α and TGF-β1 in different treatment groups in vivo. One-way ANOVA was used to determine significant differences; *p < 0.05; **p < 0.01, ***p < 0.001, compared with the indicated groups. D Immunofluorescence staining images of different macrophage markers (M1, F4/80 + CD86 + and M2, F4/80 + CD206 +) in tumor tissue sections. Scale bar: 50 µm