Corrigendum to “Design and synthesis of novel styrylquinolinium derivatives for the treatment of breast cancer: Targeting the c-Myc G-Quadruplex” [Europ. J. Med. Chem. 291 (2025) 117663]
{"title":"Corrigendum to “Design and synthesis of novel styrylquinolinium derivatives for the treatment of breast cancer: Targeting the c-Myc G-Quadruplex” [Europ. J. Med. Chem. 291 (2025) 117663]","authors":"Xutong Wang, Yu Liu, Zeyu Gao, Xiaodong Fang, Kejing Ma, Meng Sun, Qiming Li, Bing Wang, Yong Zhang, Xin Zhao, Weina Han","doi":"10.1016/j.ejmech.2025.117719","DOIUrl":null,"url":null,"abstract":"The authors regret that during the post-publication review showed that the Western Blot bands in <span><span>Fig. 11</span></span>D were pasted incorrectly, which was caused by the mismatch of file versions during the revision process. Corrected <span><span>Fig. 11</span></span> are listed below.<span><figure><span><img alt=\"Fig. 11\" aria-describedby=\"cap0010\" height=\"509\" src=\"https://ars.els-cdn.com/content/image/1-s2.0-S0223523425004842-fx1.jpg\"/><ol><li><span><span>Download: <span>Download high-res image (1MB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span><span><span><p><span>Fig. 11</span>. Evaluation of the anticancer activity of <strong>W11</strong> in human breast cancer xenografts. (A) Digital photos of mice in the control group, drug-treated group and positive control group on the 21st day of treatment. (B) Digital photos and average weight data of tumor tissue samples. (C) Fluorescence imaging of live animals in the control group, drug-treated group, and positive control group after 21 days of treatment. (D) Expression of c-Myc protein in tumor tissues of the control group, drug-treated group and positive control group after 21 days of treatment. (N ≥ 4; mean ± SD; (∗) <em>P</em> < 0.05, (∗∗) <em>P</em> < 0.01, and (∗∗∗) <em>P</em> < 0.001, significantly different from the control; ns, not significantly different from the control).</p></span></span></figure></span>","PeriodicalId":314,"journal":{"name":"European Journal of Medicinal Chemistry","volume":"25 1","pages":"117719"},"PeriodicalIF":6.0000,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Medicinal Chemistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.ejmech.2025.117719","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
Abstract
The authors regret that during the post-publication review showed that the Western Blot bands in Fig. 11D were pasted incorrectly, which was caused by the mismatch of file versions during the revision process. Corrected Fig. 11 are listed below.
Download: Download high-res image (1MB)
Download: Download full-size image
Fig. 11. Evaluation of the anticancer activity of W11 in human breast cancer xenografts. (A) Digital photos of mice in the control group, drug-treated group and positive control group on the 21st day of treatment. (B) Digital photos and average weight data of tumor tissue samples. (C) Fluorescence imaging of live animals in the control group, drug-treated group, and positive control group after 21 days of treatment. (D) Expression of c-Myc protein in tumor tissues of the control group, drug-treated group and positive control group after 21 days of treatment. (N ≥ 4; mean ± SD; (∗) P < 0.05, (∗∗) P < 0.01, and (∗∗∗) P < 0.001, significantly different from the control; ns, not significantly different from the control).
期刊介绍:
The European Journal of Medicinal Chemistry is a global journal that publishes studies on all aspects of medicinal chemistry. It provides a medium for publication of original papers and also welcomes critical review papers.
A typical paper would report on the organic synthesis, characterization and pharmacological evaluation of compounds. Other topics of interest are drug design, QSAR, molecular modeling, drug-receptor interactions, molecular aspects of drug metabolism, prodrug synthesis and drug targeting. The journal expects manuscripts to present the rational for a study, provide insight into the design of compounds or understanding of mechanism, or clarify the targets.