Journal of Cellular and Molecular MedicineVolume 26, Issue 11 p. 3309-3310 CORRIGENDUMOpen Access Corrigendum This article corrects the following: Dynamin-related protein 1-mediated mitochondrial fission contributes to IR-783-induced apoptosis in human breast cancer cells Qin Tang, Wuyi Liu, Qian Zhang, Jingbin Huang, Changpeng Hu, Yali Liu, Qing Wang, Min Zhou, Wenjing Lai, Fangfang Sheng, Guobing Li, Rong Zhang, Volume 22Issue 9Journal of Cellular and Molecular Medicine pages: 4474-4485 First Published online: July 11, 2018 First published: 06 June 2022 https://doi.org/10.1111/jcmm.17363AboutSectionsPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat In Qin Tang et al,1 the published article contains errors in Figure 4B. The correct figure is shown below. The authors state that this correction does not affect the other results of Figure 4, nor does it affect the conclusion of this article. FIGURE 4Open in figure viewerPowerPoint Knockdown of Drp1 blocked IR-783-induced mitochondrial fission, loss of MMP, ATP depletion, mPTP opening and apoptosis. (A) MDA-MB-231 cells stably expressing non-target shRNA (shCon) or Drp1 shRNA (shDrp1) were lysed and analysed by western blot. Actin was used as the loading control. (B) shCon and shDrp1 cells were treated with or without 40 μM IR-783 for 24 h. Mitochondria were then stained using MitoTracker Red CMXRos (red) and observed under a confocal microscope. Scale bars: 20 μm. (C) Average mitochondrial length was counted in 30 cells. (D) shCon and shDrp1 cells were treated with or without 40 μM IR-783 for 24 h; then, the cells were stained with rhodamine-123. The MMP was measured by fluorescence microplate. (E) Measurement of intracellular content of ATP by Luminometer Microplate reader. (F) Cells were stained with calcein-AM+CoCl2 and tested by fluorescence microplate. The calcium retention capacity (CRC) contrast to control group is an index of the opening of mPTP. (G) Cells were stained with annexin V-FITC/PE, and the percentage of apoptotic cells was measured by flow cytometry. The results were counted in three independent experiments (n = 3). Error bars represent the mean ±S.D. (*p < 0.05, **p < 0.01, ***p < 0.001) REFERENCE 1Tang Q, Liu W, Zhang Q, et al. Dynamin-related protein 1-mediated mitochondrial fission contributes to IR-783-induced apoptosis cancer cells. J Cell Mol Med. 2018; 22(9): 4474- 4485. https://doi.org/10.1111/jcmm.13749 Volume26, Issue11June 2022Pages 3309-3310 FiguresReferencesRelatedInformation