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. 2023 Dec 10;8:449. doi: 10.1038/s41392-023-01720-0

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© The Author(s) 2023

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — Posttranslational modification of ferroptosis by ubiquitination in cancer. ALL acute lymphoblastic leukemia; BAP1 tumor suppressor BRCA1-associated protein 1, BC breast cancer, CCA cholangiocarcinoma, CISD2 CDGSH iron sulfur domain 2, ccRCC clear cell renal cell carcinoma, CRC colorectal cancer, ESCC esophageal squamous cell carcinoma, GBC gallbladder cancer, GBM glioblastoma, GC gastric cancer, HCC hepatocellular carcinoma, HNRNPA2B1 heterogeneous nuclear ribonucleoprotein A2/B1, OC ovarian cancer, QSOX1 quiescin sulfhydryl oxidase 1, TEAD4 TEA domain family member 4, USP ubiquitin specific peptidase, RND1 Rho family GTPase 1, SOCS2 suppressor of cytokine signaling 2, βTrCP beta-transducin repeat containing E3 ubiqutin protein ligase