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. 2023 Apr 14;13:73. doi: 10.1186/s13578-023-01020-8

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© The Author(s) 2023

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. 6 — BCL6 promotes ferroptosis of GC cells through FZD7/β-catenin/TP63-GPX4 pathway. A BCL6, FZD7, TP63, GPX4 mRNA levels in GC cells transfected with control vector or BCL6 plasmid (*P < 0.05, **p < 0.01, ***p < 0.001). B Western blot for BCL6, FZD7, β-catenin, TP63, GPX4 and β-actin in AGS and SGC-7901 cells transfected with control vector or BCL6 plasmid. C BCL6, FZD7, TP63, GPX4 mRNA levels in AGS and SGC-7901 cells transfected with control vector (Ctrl1 + Ctrl2, Ctrl1 + FZD7, BCL6 + Ctrl2) or co-transfected BCL6 plasmid and FZD7 plasmid (BCL6 + FZD7) (**p < 0.01, ***p < 0.001). D Western blot for BCL6, FZD7, β-catenin, TP63, GPX4 and β-actin in AGS and SGC-7901 cells treated as in C