Erratum to overexpression of miR-651-5p inhibits ultraviolet radiation-induced malignant biological behaviors of sebaceous gland carcinoma cells by targeting ZEB2
Erratum to: Ann Transl Med 2022;10:517
This article (1) titled “Overexpression of miR-651-5p inhibits ultraviolet radiation-induced malignant biological behaviors of sebaceous gland carcinoma cells by targeting ZEB2” (doi: 10.21037/atm-21-3897), unfortunately contain errors in the authorship section, the legend of Figure 2, Figure 3 and its legend, Figure 4, Figure 5 and its legend, and the legend of Figure 7.
Christos C. Zouboulis’s name is missing in the authorship section. He should be listed as the eighth author and his affiliation should be labeled 3.
The corrected authorship section is as follows:
Haiyan Zhao1,2, Xiaochun Yang2, Juan Liu2, Fang Han2, Zhengrong Yang2, Zhongyin Hu2, Mingzhi Liu2, Christos C. Zouboulis3, Yan Mei1,2^
1Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming, China; 2Department of Ophthalmology, The Affiliated Hospital of Kunming University of Science and Technology, The First People’s Hospital of Yunnan Province, Kunming, China; 3Departments of Dermatology, Venereology, Allergology and Immunology, Dessau Medical Center, Brandenburg Medical School Theodor Fontane and Faculty of Health Sciences Brandenburg, Dessau, Germany
In the legend of Figure 2, Figure 5 and Figure 7, the description “The cells were cultured by Transwell method and stained with crystal violet, and the migration ability of SGC cells was determined under UV irradiation” should be corrected to “The cells were cultured by Transwell method and stained with crystal violet, and the migration and invasion ability of SGC cells was determined under UV irradiation”.
Figure 3 should be updated, and the first and the second sentences in the legend of Figure 3 should be corrected from “Effect of miR-136-5p and miR-651-5p overexpression on the apoptosis of UV-induced SGC cells” to “Effect of miR-651-5p expression on the apoptosis of UV-induced SGC cells. (A,B) “Expression of miR-136-5p in SGC cells in each group was measured by RT-qPCR” to “Expression of miR-651-5p in SGC cells in each group was measured by RT-qPCR”.
Figure 4 and Figure 5 should be updated as well.
The corrected legend of Figure 2, Figure 3 and its legend, Figure 4, Figure 5 and its legend, and the legend of Figure 7 are as follows:
Corrected legend of Figure 2:
Figure 2 Effect of UV exposure on the apoptosis, invasion, migration, and EMT of SGC cells. (A) Expression of miR-651-5p in SGC cells after treatment with different doses of UV radiation was measured by RT-qPCR. (B,C) Apoptosis of UV-treated SGC cells was measured by flow cytometry and TUNEL staining. Magnification of 200×. (D,E) The cells were cultured by Transwell method and stained with crystal violet, and the migration and invasion ability of SGC cells was determined under UV irradiation. Magnification of 200×. (F) Expression levels of proteins related to EMT in UV-induced SGC cells were measured by western blotting. *P<0.05 and **P<0.01 vs. the 0 mJ/cm2 group; by one-way ANOVA. UV, ultraviolet; TUNEL, terminal deoxynucleotidyl transferase dUTP nick-end labeling; EMT, epithelial-mesenchymal transition; SGC, sebaceous gland carcinoma; RT-qPCR, real-time quantitative polymerase chain reaction; ANOVA, analysis of variance.
Corrected Figure 3 and its legend:
Figure 3 Effect of miR-651-5p expression on the apoptosis of UV-induced SGC cells. (A,B) Expression of miR-651-5p in SGC cells in each group was measured by RT-qPCR. **P<0.01 vs. the mimics-NC or inhibitors-NC group; #P<0.05 and ##P<0.01 vs. the NC group; two-way ANOVA. (C,D) Apoptosis of SGC cells after UV treatment was measured by flow cytometry and TUNEL. Magnification of 200×. **P<0.01 vs. the NC group; ##P<0.01 vs. the UV group; two-way ANOVA or one-way ANOVA. NC, normal control; UV, ultraviolet; TUNEL, terminal deoxynucleotidyl transferase dUTP nick-end labeling; SGC, sebaceous gland carcinoma; RT-qPCR, real-time quantitative polymerase chain reaction; ANOVA, analysis of variance.
Corrected Figure 4:
Corrected Figure 5 and its legend:
Figure 5 Knockdown of ZEB2 affected the invasion, migration, and EMT of UV-induced SGC cells. (A) Expression of ZEB2 was measured by western blotting. (B,C) Apoptosis of UV-treated SGC cells was measured by flow cytometry and TUNEL staining. Magnification of 200×. (D,E) The cells were cultured by Transwell method and stained with crystal violet, and the migration and invasion ability of SGC cells was determined under UV irradiation. Magnification of 200×. (F) Expression levels of proteins related to EMT in UV-induced SGC cells were measured by western blotting. *P<0.05 and **P<0.01 vs. the NC group; #P<0.05 and ##P<0.01 vs. the UV group; by one-way ANOVA. ZEB2, zinc finger E-box binding homeobox 2; NC, normal control; UV, ultraviolet; TUNEL, terminal deoxynucleotidyl transferase dUTP nick-end labeling; EMT, epithelial-mesenchymal transition; SGC, sebaceous gland carcinoma; RT-qPCR, real-time quantitative polymerase chain reaction; ANOVA, analysis of variance.
Corrected legend of Figure 7:
Figure 7 Role of ZEB2 in the inhibition of the malignant biological behavior of UV-induced SGC by miR-651-5p overexpression in vivo and in vitro. (A,B) Apoptosis of UV-treated SGC cells in each group was measured by flow cytometry and TUNEL staining. Magnification of 200×. (C,D) The cells were cultured by Transwell method and stained with crystal violet, and the migration and invasion ability of SGC cells was determined under UV irradiation. Magnification of 200×. (E) Expression levels of ZEB2 and proteins related to EMT in SGC cells after UV treatment in each group were measured by western blotting. (F) Representative images of tumors from the implanted mice are shown. (G) Time course of changes in tumor volume of the implanted mice. (H) Tumor weights of the implanted mice. *P<0.05 and **P<0.01 vs. the UV group; #P<0.05 and ##P<0.01 vs. the miR-651-5p mimics group; one-way ANOVA or two-way ANOVA. UV, ultraviolet; ZEB2, zinc finger E-box binding homeobox 2; TUNEL, terminal deoxynucleotidyl transferase dUTP nick-end labeling; NC, normal control; SGC, sebaceous gland carcinoma; EMT, epithelial-mesenchymal transition; ANOVA, analysis of variance.
The authors apologize for the oversight.
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References
- Zhao H, Yang X, Liu J, et al. Overexpression of miR-651-5p inhibits ultraviolet radiation-induced malignant biological behaviors of sebaceous gland carcinoma cells by targeting ZEB2. Ann Transl Med 2022;10:517. [Crossref] [PubMed]
