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. 2023 Dec 11;14(12):815. doi: 10.1038/s41419-023-06352-4

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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. 1 — A, B Expression of Mint3 in MDA-MB-231 (A) and MDA-MB-468 cells (B) expressing doxycycline-inducible shRNAs against Mint3 (ishMint3) treated with doxycycline (1 μg/ml) for 3 days. C, D Cytotoxicity assay of control (DOX(−)) and doxycycline-pre-treated (DOX (+)) MDA-MB-231 (C) and MDA-MB-468 (D) ishMint3 cells in the presence of doxorubicin (DXR) for 24 h at the indicated concentration. E, F Cytotoxicity assay of control (DOX(−)) and doxycycline-pre-treated (DOX(+)) MDA-MB-231 (E) and MDA-MB-468 (F) ishMint3 cells in the presence of paclitaxel (PTX) for 24 h at the indicated concentration. In C–F, the data represent the mean ± SD (n = 3).