- 1Department of Obstetrics & Gynecology, The Second Affiliated Hospital of Nanchang University, Nanchang, China
- 2Department of Obstetrics & Gynecology, The First Affiliated Hospital of Nanchang University, Nanchang, China
- 3Institute of Translational Medicine, Nanchang University, Nanchang, China
By Le F, Yang L, Han Y, Zhong Y, Zhan F, Feng Y, Hu H, Chen T and Tan B (2021) Front. Oncol. 11:704001. doi: 10.3389/fonc.2021.704001
There was a mistake in Figure 3 as published. In Figure 3C, there are instances of duplicated areas between some images due to carelessness. Specifically, these occur between: Migration-C and Invasion-Co-C; Invasion-C and Migration-12.5nM TPL; Invasion-C and Invasion-6.25nM TPL; Invasion-Co-C and Invasion-12.5nM TPL; Invasion-6.25nM TPL and Migration-25nM TPL; Invasion-6.25nM TPL and Migration-12.5nM TPL. The corrected Figure 3 appears below.

Figure 3. Tumor-associated macrophage (TAM) cell supernatant slightly improves the proliferation, migration, and invasiveness of A2780/DDP cells, but triptolide (TPL) reverses these effects. (A) TPL was diluted to varying concentrations with TAM cell supernatant, and then added to A2780/DDP cells; cell proliferative ability was measured 24 h later. (B) Quantitative analyses of the proliferative capacity of A2780/DDP cells are shown in (A). (C) Representative transwell migration and invasion assay of A2780/DDP cells after treatment with TPL. (D, E) Quantification of migratory and invasive capacities of A2780/DDP in (C). *P < 0.05, **P < 0.01, and ***P < 0.001. (F, G) Representative extracellular matrix-adhesion experiment using A2780/DDP cells treated with different concentrations of TPL for 3 or 6 h. *P < 0.05. ns, no significance.
The original version of this article has been updated.
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Keywords: A2780/DDP cells, cisplatin (DDP) resistance, triptolide (TPL), PI3K/AKT/NF-κB- pathway, tumor-associated macrophages (TAMs)
Citation: Le F, Yang L, Han Y, Zhong Y, Zhan F, Feng Y, Hu H, Chen T and Tan B (2025) Correction: TPL inhibits the invasion and migration of drug-resistant ovarian cancer by targeting the PI3K/AKT/NF-κB-signaling pathway to inhibit the polarization of M2 TAMs. Front. Oncol. 15:1641399. doi: 10.3389/fonc.2025.1641399
Received: 05 June 2025; Accepted: 20 August 2025;
Published: 08 September 2025.
Approved by:
Frontiers Editorial Office, Frontiers Media SA, SwitzerlandCopyright © 2025 Le, Yang, Han, Zhong, Zhan, Feng, Hu, Chen and Tan. 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: Tingtao Chen, Y2hlbnRpbmd0YW8xOTg0QDE2My5jb20=; Buzhen Tan, dGFuYnV6aGVuQHNpbmEuY29t; Hui Hu, aHVodWkyMDA4QDE2My5jb20=
†These authors have contributed equally to this work and share first authorship