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CORRECTION article

Front. Cell Dev. Biol., 10 September 2025

Sec. Cell Death and Survival

Volume 13 - 2025 | https://doi.org/10.3389/fcell.2025.1685448

Correction: Cooperative targeting of NF-κB enhances ferroptosis-driven HCC therapy with Alisertib and Donafenib

Qiong ZhouQiong ZhouRui Wang
Rui Wang*
  • Laboratory of Medical Oncology, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, Jiangsu, China

A Correction on
Cooperative targeting of NF-κB enhances ferroptosis-driven HCC therapy with Alisertib and Donafenib

by Zhou Q and Wang R (2025). Front. Cell Dev. Biol. 13:1637767. doi: 10.3389/fcell.2025.1637767

There was a mistake in Figure 3I as published. During the proofing process, the image intended to represent the p65 WB bands from Huh7 cells was mistakenly duplicated, which resulted in the appearance of incorrect images in Figure 3I. We have since conducted a thorough review of all original bands and have confirmed that the original images were accurate and did not contain any duplication. This error was unintentional and occurred during the image compilation. Importantly, this correction does not affect the conclusions drawn from our experiments. The corrected Figure 3 appears below.

Figure 3
A collection of scientific data visualizations and experimental results related to cell death and gene expression studies. The figures include a principal component analysis plot (A), a bar graph depicting differentially expressed genes (B), a volcano plot illustrating gene expression changes (C), KEGG pathway analysis (D), and GSVA scores for various cell death types (E,F). Additional data show pathway correlations in tumors (G) and ferroptosis analysis (H). Western blot images (I,J) and corresponding bar graphs (K-R) reveal protein expression levels in different conditions. Confocal microscopy images (S,T) display cellular localization of proteins with DAPI and p65 staining.

Figure 3. The Synergistic Effect of Alisertib and Donafenib on Ferroptosis in Hepatocellular Carcinoma Cells Mediated by the NF-κB Signaling Pathway. (A) PCA analysis of sequencing samples from HCCLM3 cells. (B) Upset plot illustrates the DEGs (p < 0.05, |log2FC|>1) across treatment groups. (C) Volcano plot highlights DEGs significantly in 1555 genes (p < 0.05, |log2FC|>2). (D) KEGG enriched pathways in synergy. (E) Heatmap for PCD scores across HCCLM3. (F) Enrichment scores for PCD in TCGA LIHC samples. (G) Correlation between ferroptosis scores and the NF-κB signaling pathway across 33 tumor types in TCGA and (H) in LIHC from TCGA. (I) NF-κB signaling molecules (p65, IκBα, p-p65, p-IκBα) with quantitative analyses for (K) p65, (L) IκBα, (M) p-p65, (N) p-IκBα, and (O) ratios of p-p65/p65 and (P) p-IkBa/IkBa. (J) cytoplasmic and nuclear p65 expression, including quantitative results for (Q) cytoplasmic p65 and (R) nuclear p65. (S, T) p65 nuclear translocation in HCCLM3 and Huh7 cells. (n = 3, *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001, ns, non-significant; DFN, Donafenib; Alis, Alisertib).

The original version of this article has been updated.

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Keywords: hepatocellular carcinoma, Donafenib, Alisertib, ferroptosis, NF-κB signaling pathway

Citation: Zhou Q and Wang R (2025) Correction: Cooperative targeting of NF-κB enhances ferroptosis-driven HCC therapy with Alisertib and Donafenib. Front. Cell Dev. Biol. 13:1685448. doi: 10.3389/fcell.2025.1685448

Received: 13 August 2025; Accepted: 27 August 2025;
Published: 10 September 2025.

Edited and reviewed by:

Junqi Huang, Jinan University, China

Copyright © 2025 Zhou and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Rui Wang, d2FuZ3J1aTIxOEBuanUuZWR1LmNu

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.