Tengfei Fan1,2,3, Xiaoning Wang1,4, Sheng Zhang3, Ping Deng5, Yi Jiang6, Yidan Liang7, Sheng Jie5, Qing Wang3, Chuwen Li1, Guocai Tian1, Zhen Zhang1, Zhenhu Ren1,2, Bo Li8, Yanrong Chen3, Zhijing He3, Yan Luo5, Mingliang Chen9, Hanjiang Wu3, Zhengping Yu5, Huifeng Pi10, Zhou Zhou11, Zhiyuan Zhang12. 1. Department of Oral and Maxillofacial-Head Neck Oncology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine; College of Stomatology, Shanghai Jiao Tong University; National Center for Stomatology; National Clinical Research Center for Oral Diseases; Shanghai Key Laboratory of Stomatology; Research Unit of Oral and Maxillofacial Regenerative Medicine, Chinese Academy of Medical Sciences, Shanghai, China. 2. Department of Oral and Maxillofacial Surgery, Zhang Zhiyuan Academician Workstation, Hainan Western Central Hospital, Shanghai Ninth People's Hospital, Danzhou, Hainan, China. 3. Department of Oral and Maxillofacial Surgery, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China. 4. Department of Oral Pathology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. 5. Department of Occupational Health, Third Military Medical University, Chongqing, China. 6. Department of Pathology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China. 7. School of Medicine, Guangxi University, Nanning, Guangxi Zhuang Autonomous Region, China. 8. Department of Oral and Maxillofacial Surgery, Affiliated Hospital of Guilin Medical University, Guilin, Guangxi Zhuang Autonomous Region, China. 9. Institute of Pathology and Southwest Cancer Centre, Southwest Hospital, Third Military Medical University, Chongqing, China. 10. Department of Occupational Health, Third Military Medical University, Chongqing, China. pihuifeng2010@163.com. 11. Department of Emergency Medicine, First Affiliated Hospital and Department of Environmental Medicine, School of Public Health, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China. lunazhou@zju.edu.cn. 12. Department of Oral and Maxillofacial-Head Neck Oncology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine; College of Stomatology, Shanghai Jiao Tong University; National Center for Stomatology; National Clinical Research Center for Oral Diseases; Shanghai Key Laboratory of Stomatology; Research Unit of Oral and Maxillofacial Regenerative Medicine, Chinese Academy of Medical Sciences, Shanghai, China. zhzhy0502@163.com.
Correction to: Signal Transduction and Targeted Therapy 10.1038/s41392-022-00939-7, published online 25 April 2022In the process of checking the raw data[1], the authors noticed several inadvertent mistakes occurring in Fig. 5a, b, c, d, f that need to be corrected after online publication of the article. During the preparation of Fig. 5, the representative image showing TFE3 overexpression antagonized the NUPR1 KD-induced inhibition of OSCC cell proliferation and metastasis, were pasted and placed by mistake. The correct results should be as shown below. The authors apologize for these oversights and declare that these corrections do not affect the description, interpretation, or conclusions detailed in the original manuscript.
Fig. 5
a, b Representative images of colony formation and quantitative analysis results in NUPR1 KD or scrambled Cal27 and HN6 cells transfected with TFE3 plasmid or a control plasmid for 24 h; n = 4. c, d The migration results for of NUPR1 KD or scrambled Cal27 and HN6 cells transfected with TFE3 plasmid or a control plasmid; scale bar: 100 μm. e, f The invasion results for NUPR1 KD or scrambled Cal27 and HN6 cells transfected with TFE3 plasmid or a control plasmid. Scale bar = 80 μm; magnification; n = 4; 40×;
a, b Representative images of colony formation and quantitative analysis results in NUPR1 KD or scrambled Cal27 and HN6 cells transfected with TFE3 plasmid or a control plasmid for 24 h; n = 4. c, d The migration results for of NUPR1 KD or scrambled Cal27 and HN6 cells transfected with TFE3 plasmid or a control plasmid; scale bar: 100 μm. e, f The invasion results for NUPR1 KD or scrambled Cal27 and HN6 cells transfected with TFE3 plasmid or a control plasmid. Scale bar = 80 μm; magnification; n = 4; 40×;