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Updated: Sep 19, 2026

Live-imaging of Breast Epithelial Cell Migration After the Transient Depletion of TIP60
Published on: December 7, 2017
[Corrigendum] TIP60 governs the auto‑ubiquitination of UHRF1 through USP7 dissociation from the UHRF1/USP7 complex
Tanveer Ahmad1, Waseem Ashraf1, Abdulkhaleg Ibrahim2
1Laboratory of Bioimaging and Pathologies, CNRS UMR‑7021, Faculty of Pharmacy, University of Strasbourg, 67401 Illkirch, France.
Abstract:
Following the publication of the above article, and an Expression of Concern statement (doi: 10.3892/ijo.2026.5908) that was published in light of the fact that the GAPDH control western blots shown in Fig. 5A on p. 9 were strikingly similar to the GAPDH control western blots shown in Fig. 5D, the authors have responded to the queries raised by the Editorial Office. The GAPDH panels shown in Figs. 5A and 5D were generated from the same experiment and the same set of protein lysates: Fig. 5A presented the analysis of total protein expression, whereas Fig. 5D presented immunoprecipitation analyses performed using material derived from these same experimental samples. Consequently, the GAPDH loading control was legitimately shared between the two figures. However, given that the original figure legend did not explicitly state that the same GAPDH loading control was used for both analyses, to eliminate any possible ambiguity for readers, the authors have revised Fig. 5 by replacing the representative '-MG132 panel' in Fig. 5A with results obtained from an independent repeat experiment performed under identical experimental conditions. The revised version of Fig. 5 is shown on the next page. Note that this revised figure reproduces the original findings, and does not affect the quantitative analyses, the interpretation of the data, or the conclusions of the study. Regarding a query raised by the Editorial Office concerning the presentation of flow cytometric plots in Fig. 8, the authors explained that Fig. 8E was generated by applying an additional fluorescence gate to the parent flow cytometry dataset shown in Fig. 8B, which represents standard flow cytometric analysis, rather than duplication of experimental data, and so this figure was presented correctly, and as intended by the authors. The authors thank the Editor of International Journal of Oncology for granting them the opportunity to publish this corrigendum, and all the authors agree with its publication. [International Journal of Oncology 59: 89, 2021; DOI: 10.3892/ijo.2021.5269].
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