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. 2022 Feb 10;21:43. doi: 10.1186/s12943-022-01519-7

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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. 5 — The expression of METTL7B was positively correlated with GPX4, SOD1 and HMOX1. a The tumors in Fig. 2e were used to measure the expressions of METTL7B, GPX4, SOD1 and HMOX1 by immunohistochemistry. Scale bar: 100 μm. b The correlation between METTL7B and GPX4, SOD1 and HMOX1 in LUAD tissues from TCGA database. *P < 0.05