{"title":"撤回:MiRNA-545负调控胃癌中EMS1的致癌活性","authors":"","doi":"10.1002/cam4.71011","DOIUrl":null,"url":null,"abstract":"<div>\n \n <section>\n \n <p>\n <b>RETRACTION</b>: <span>M. Ma</span>, <span>J. Zhao</span>, <span>Q. Wu</span>, <span>K. Xiao</span>, <span>S. Li</span>, <span>H. Zhu</span>, <span>C. Liu</span>, <span>H. Xie</span>, and <span>C. Zuo</span>, “ <span>MiRNA-545 Negatively Regulates the Oncogenic Activity of EMS1 in Gastric Cancer</span>,” <i>Cancer Medicine</i> <span>7</span>, no. <span>6</span> (<span>2018</span>): <span>2452</span>–<span>2462</span>, https://doi.org/10.1002/cam4.1520.\n </p>\n </section>\n \n <section>\n \n <p>The above article, published online on 07 May 2018 in Wiley Online Library (wileyonlinelibrary.com), has been retracted by agreement between the authors; the journal Editor-in-Chief, Stephen Tait; and John Wiley & Sons Ltd.</p>\n </section>\n \n <section>\n \n <p>The retraction has been agreed due to the use of contaminated cell lines in this article. Both the cell lines used to demonstrate the regulatory role of miR-545 in EMS1 expression (SGC-7901 & BGC-823) have been reported to be contaminated with HeLa [1, 2], as has cell line MGC-803 [3, 4]. Thus, the editors consider the conclusions of this article to be invalid.</p>\n </section>\n \n <section>\n \n <p>We did not find any evidence of misconduct by the authors.</p>\n </section>\n \n <section>\n \n <h3> References</h3>\n \n <p>\n [1] <span>F. Ye</span>, <span>C. Chen</span>, <span>J. Qin</span>, <span>J. Liu</span>, and <span>C. Zheng</span>, “ <span>Genetic Profiling Reveals an Alarming Rate of Cross-Contamination Among Human Cell Lines Used in China</span>,” <i>The FASEB Journal</i> <span>29</span>, no. <span>10</span> (<span>2015</span>): <span>4268</span>–<span>4272</span>, https://doi.org/10.1096/fj.14-266718.\n </p>\n \n <p>\n [2] <span>X. Bian</span>, <span>Z. Yang</span>, <span>H. Feng</span>, <span>H. Sun</span>, and <span>Y. Liu</span>, “ <span>A Combination of Species Identification and STR Profiling Identifies Cross-contaminated Cells from 482 Human Tumor Cell Lines</span>,” <i>Scientific Reports</i> <span>7</span> (<span>2017</span>): <span>9774</span>, https://doi.org/10.1038/s41598-017-09660-w.\n </p>\n \n <p>\n [3] <span>F. Cao</span>, <span>H. Sun</span>, <span>Z. Yang</span>, <span>Y. Bai</span>, <span>X. Hu</span>, <span>Y. Hou</span>, <span>X. Bian</span>, and <span>Y. Liu</span>, “ <span>Multiple Approaches Revealed MGc80-3 as a Somatic Hybrid with HeLa Cells Rather than a Gastric Cancer Cell Line</span>,” <i>International Journal of Cancer</i> <span>154</span>, no. <span>1</span> (<span>2024</span>): <span>155</span>–<span>168</span>, https://doi.org/10.1002/ijc.34677.\n </p>\n \n <p>\n [4] <span>M. Yang</span>, <span>J. He</span>, <span>S. Xia</span>, <span>Y. Wang</span>, <span>J. Xiong</span>, <span>C. Liao</span>, <span>N. Li</span>, <span>S. Qu</span>, and <span>C. Shen</span>, \" <span>Investigation of the Mixed Origins of the MGC-803 Cell Line Reveals That It Is a Hybrid Cell Line Derived from HeLa</span>,\" <i>Human Cell</i> <span>37</span> (<span>2024</span>): <span>560</span>–<span>566</span>, https://doi.org/10.1007/s13577-023-01011-4.\n </p>\n </section>\n </div>","PeriodicalId":139,"journal":{"name":"Cancer Medicine","volume":"14 13","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cam4.71011","citationCount":"0","resultStr":"{\"title\":\"RETRACTION: MiRNA-545 Negatively Regulates the Oncogenic Activity of EMS1 in Gastric Cancer\",\"authors\":\"\",\"doi\":\"10.1002/cam4.71011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <section>\\n \\n <p>\\n <b>RETRACTION</b>: <span>M. Ma</span>, <span>J. Zhao</span>, <span>Q. Wu</span>, <span>K. Xiao</span>, <span>S. 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RETRACTION: MiRNA-545 Negatively Regulates the Oncogenic Activity of EMS1 in Gastric Cancer
RETRACTION: M. Ma, J. Zhao, Q. Wu, K. Xiao, S. Li, H. Zhu, C. Liu, H. Xie, and C. Zuo, “ MiRNA-545 Negatively Regulates the Oncogenic Activity of EMS1 in Gastric Cancer,” Cancer Medicine7, no. 6 (2018): 2452–2462, https://doi.org/10.1002/cam4.1520.
The above article, published online on 07 May 2018 in Wiley Online Library (wileyonlinelibrary.com), has been retracted by agreement between the authors; the journal Editor-in-Chief, Stephen Tait; and John Wiley & Sons Ltd.
The retraction has been agreed due to the use of contaminated cell lines in this article. Both the cell lines used to demonstrate the regulatory role of miR-545 in EMS1 expression (SGC-7901 & BGC-823) have been reported to be contaminated with HeLa [1, 2], as has cell line MGC-803 [3, 4]. Thus, the editors consider the conclusions of this article to be invalid.
We did not find any evidence of misconduct by the authors.
References
[1] F. Ye, C. Chen, J. Qin, J. Liu, and C. Zheng, “ Genetic Profiling Reveals an Alarming Rate of Cross-Contamination Among Human Cell Lines Used in China,” The FASEB Journal29, no. 10 (2015): 4268–4272, https://doi.org/10.1096/fj.14-266718.
[2] X. Bian, Z. Yang, H. Feng, H. Sun, and Y. Liu, “ A Combination of Species Identification and STR Profiling Identifies Cross-contaminated Cells from 482 Human Tumor Cell Lines,” Scientific Reports7 (2017): 9774, https://doi.org/10.1038/s41598-017-09660-w.
[3] F. Cao, H. Sun, Z. Yang, Y. Bai, X. Hu, Y. Hou, X. Bian, and Y. Liu, “ Multiple Approaches Revealed MGc80-3 as a Somatic Hybrid with HeLa Cells Rather than a Gastric Cancer Cell Line,” International Journal of Cancer154, no. 1 (2024): 155–168, https://doi.org/10.1002/ijc.34677.
[4] M. Yang, J. He, S. Xia, Y. Wang, J. Xiong, C. Liao, N. Li, S. Qu, and C. Shen, " Investigation of the Mixed Origins of the MGC-803 Cell Line Reveals That It Is a Hybrid Cell Line Derived from HeLa," Human Cell37 (2024): 560–566, https://doi.org/10.1007/s13577-023-01011-4.
期刊介绍:
Cancer Medicine is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research from global biomedical researchers across the cancer sciences. The journal will consider submissions from all oncologic specialties, including, but not limited to, the following areas:
Clinical Cancer Research
Translational research ∙ clinical trials ∙ chemotherapy ∙ radiation therapy ∙ surgical therapy ∙ clinical observations ∙ clinical guidelines ∙ genetic consultation ∙ ethical considerations
Cancer Biology:
Molecular biology ∙ cellular biology ∙ molecular genetics ∙ genomics ∙ immunology ∙ epigenetics ∙ metabolic studies ∙ proteomics ∙ cytopathology ∙ carcinogenesis ∙ drug discovery and delivery.
Cancer Prevention:
Behavioral science ∙ psychosocial studies ∙ screening ∙ nutrition ∙ epidemiology and prevention ∙ community outreach.
Bioinformatics:
Gene expressions profiles ∙ gene regulation networks ∙ genome bioinformatics ∙ pathwayanalysis ∙ prognostic biomarkers.
Cancer Medicine publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper.