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International Journal of Oncology
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Print ISSN: 1019-6439 Online ISSN: 1791-2423
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April-2022 Volume 60 Issue 4

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International Journal of Molecular Medicine

International Journal of Molecular Medicine

International Journal of Molecular Medicine is an international journal devoted to molecular mechanisms of human disease.

International Journal of Oncology

International Journal of Oncology

International Journal of Oncology is an international journal devoted to oncology research and cancer treatment.

Molecular Medicine Reports

Molecular Medicine Reports

Covers molecular medicine topics such as pharmacology, pathology, genetics, neuroscience, infectious diseases, molecular cardiology, and molecular surgery.

Oncology Reports

Oncology Reports

Oncology Reports is an international journal devoted to fundamental and applied research in Oncology.

Experimental and Therapeutic Medicine

Experimental and Therapeutic Medicine

Experimental and Therapeutic Medicine is an international journal devoted to laboratory and clinical medicine.

Oncology Letters

Oncology Letters

Oncology Letters is an international journal devoted to Experimental and Clinical Oncology.

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Explores a wide range of biological and medical fields, including pharmacology, genetics, microbiology, neuroscience, and molecular cardiology.

Molecular and Clinical Oncology

Molecular and Clinical Oncology

International journal addressing all aspects of oncology research, from tumorigenesis and oncogenes to chemotherapy and metastasis.

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World Academy of Sciences Journal

Multidisciplinary open-access journal spanning biochemistry, genetics, neuroscience, environmental health, and synthetic biology.

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International Journal of Functional Nutrition

Open-access journal combining biochemistry, pharmacology, immunology, and genetics to advance health through functional nutrition.

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International Journal of Epigenetics

Publishes open-access research on using epigenetics to advance understanding and treatment of human disease.

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Correction Open Access

[Corrigendum] Knockdown of SNHG15 suppresses renal cell carcinoma proliferation and EMT by regulating the NF‑κB signaling pathway

  • Authors:
    • Yang Du
    • Chuize Kong
    • Yuyan Zhu
    • Meng Yu
    • Zeliang Li
    • Jianbin Bi
    • Zhenhua Li
    • Xiankui Liu
    • Zhe Zhang
    • Xiuyue Yu
  • View Affiliations / Copyright

    Affiliations: Department of Urology, The First Hospital of China Medical University, Shenyang, Liaoning 110001, P.R. China, Department of Reproductive Biology and Transgenic Animal China Medical University, Shenyang, Liaoning 110003, P.R. China
    Copyright: © Du et al. This is an open access article distributed under the terms of Creative Commons Attribution License [CC BY 4.0].
  • Article Number: 36
    |
    Published online on: February 21, 2022
       https://doi.org/10.3892/ijo.2022.5326
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Article

Int J Oncol 53: [Related article:] 384-394, 2018; DOI: 10.3892/ijo.2018.4395

Subsequently to the publication of the above article, the authors have realized that, on p. 390, the data selected for the siRNA-1 and siRNA-2 experiments for the ACHN and 786-O cell lines concerning both the invasion and the migration assays in Fig. 4B were selected inappropriately. Furthermore, after having inspected the published version of Fig. 5, the authors have realized that, for the immunofluorescence experiments shown in Fig. 5D, the first 'Merged' pictures for the first two columns of the ACHN cell line were accidentally published in the wrong order.

Figure 4

SNHG15 promotes renal cell carcinoma migration and invasion. (A) Morphological alterations of SNHG15 knockdown cells, as detected under an optical microscope (magnification, ×10). (B) Transwell assays were used to determine the migration and invasion of ACHN and 786-O cells transfected with siRNAs (magnification, ×40). *P<0.01. (C) Expression levels of cell adhesion molecules (E-cadherin, N-cadherin and Vimentin), as detected in 786-O and ACHN cells. *P<0.01. NC, negative control; siRNA, small interfering RNA; SNHG15, small nucleolar RNA host gene 15.

Figure 5

Knockdown of SNHG15 affects NF-κB entry into the nucleus. (A) Knockdown of SNHG15 reduced the protein expression levels of EMT-associated transcription factors (Snail1, Slug and ZEB1). However, there was no difference in the total protein expression levels of NF-κB between the SNHG15 siRNA and NC groups. *P<0.01; nsP>0.05. (B) Nuclear/cytoplasmic NF-κB expression in ACHN and 786-O cells transfected with siRNAs. *P<0.01. (C) Following stimulation with TNF-α for 6 h, EMT markers were examined among the various groups. *P<0.01. (D) Nuclear immunofluorescence intensity of NF-κB was reduced in the SNHG15 siRNA groups compared with in the NC groups. (E) Cell migration and invasion were altered among the various groups following TNF-α stimulation and siRNA transfection (magnification, ×40). *P<0.01. EMT, epithelial-mesenchymal transition; NC, negative control; NF-κB, nuclear factor-κB; siRNA, small interfering RNA; SNHG15, small nucleolar RNA host gene 15; TNF-α, tumor necrosis factor-α; ZEB1, zinc finger E-box-binding homeobox 1

The corrected versions of Figs. 4, and 5, including all the correct data for Figs. 4B and 5D, are shown on the next three pages. The authors confirm that these data continue to support the main conclusions presented in their paper, and are grateful to the Editor of International Journal of Oncology for granting them this opportunity to publish a Corrigendum. They also apologize to the readership for any inconvenience caused.

Figure 4

SNHG15 promotes renal cell carcinoma migration and invasion. (A) Morphological alterations of SNHG15 knockdown cells, as detected under an optical microscope (magnification, ×10). (B) Transwell assays were used to determine the migration and invasion of ACHN and 786-O cells transfected with siRNAs (magnification, ×40). *P<0.01. (C) Expression levels of cell adhesion molecules (E-cadherin, N-cadherin and Vimentin), as detected in 786-O and ACHN cells. *P<0.01. NC, negative control; siRNA, small interfering RNA; SNHG15, small nucleolar RNA host gene 15.

Figure 5

Knockdown of SNHG15 affects NF-κB entry into the nucleus. (A) Knockdown of SNHG15 reduced the protein expression levels of EMT-associated transcription factors (Snail1, Slug and ZEB1). However, there was no difference in the total protein expression levels of NF-κB between the SNHG15 siRNA and NC groups. *P<0.01; nsP>0.05. (B) Nuclear/cytoplasmic NF-κB expression in ACHN and 786-O cells transfected with siRNAs. *P<0.01. (C) Following stimulation with TNF-α for 6 h, EMT markers were examined among the various groups. *P<0.01. (D) Nuclear immunofluorescence intensity of NF-κB was reduced in the SNHG15 siRNA groups compared with in the NC groups. (E) Cell migration and invasion were altered among the various groups following TNF-α stimulation and siRNA transfection (magnification, ×40). *P<0.01. EMT, epithelial-mesenchymal transition; NC, negative control; NF-κB, nuclear factor-κB; siRNA, small interfering RNA; SNHG15, small nucleolar RNA host gene 15; TNF-α, tumor necrosis factor-α; ZEB1, zinc finger E-box-binding homeobox 1

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Copy and paste a formatted citation
Spandidos Publications style
Du Y, Kong C, Zhu Y, Yu M, Li Z, Bi J, Li Z, Liu X, Zhang Z, Yu X, Yu X, et al: [Corrigendum] Knockdown of SNHG15 suppresses renal cell carcinoma proliferation and EMT by regulating the NF‑κB signaling pathway. Int J Oncol 60: 36, 2022.
APA
Du, Y., Kong, C., Zhu, Y., Yu, M., Li, Z., Bi, J. ... Yu, X. (2022). [Corrigendum] Knockdown of SNHG15 suppresses renal cell carcinoma proliferation and EMT by regulating the NF‑κB signaling pathway. International Journal of Oncology, 60, 36. https://doi.org/10.3892/ijo.2022.5326
MLA
Du, Y., Kong, C., Zhu, Y., Yu, M., Li, Z., Bi, J., Li, Z., Liu, X., Zhang, Z., Yu, X."[Corrigendum] Knockdown of SNHG15 suppresses renal cell carcinoma proliferation and EMT by regulating the NF‑κB signaling pathway". International Journal of Oncology 60.4 (2022): 36.
Chicago
Du, Y., Kong, C., Zhu, Y., Yu, M., Li, Z., Bi, J., Li, Z., Liu, X., Zhang, Z., Yu, X."[Corrigendum] Knockdown of SNHG15 suppresses renal cell carcinoma proliferation and EMT by regulating the NF‑κB signaling pathway". International Journal of Oncology 60, no. 4 (2022): 36. https://doi.org/10.3892/ijo.2022.5326
Copy and paste a formatted citation
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Spandidos Publications style
Du Y, Kong C, Zhu Y, Yu M, Li Z, Bi J, Li Z, Liu X, Zhang Z, Yu X, Yu X, et al: [Corrigendum] Knockdown of SNHG15 suppresses renal cell carcinoma proliferation and EMT by regulating the NF‑κB signaling pathway. Int J Oncol 60: 36, 2022.
APA
Du, Y., Kong, C., Zhu, Y., Yu, M., Li, Z., Bi, J. ... Yu, X. (2022). [Corrigendum] Knockdown of SNHG15 suppresses renal cell carcinoma proliferation and EMT by regulating the NF‑κB signaling pathway. International Journal of Oncology, 60, 36. https://doi.org/10.3892/ijo.2022.5326
MLA
Du, Y., Kong, C., Zhu, Y., Yu, M., Li, Z., Bi, J., Li, Z., Liu, X., Zhang, Z., Yu, X."[Corrigendum] Knockdown of SNHG15 suppresses renal cell carcinoma proliferation and EMT by regulating the NF‑κB signaling pathway". International Journal of Oncology 60.4 (2022): 36.
Chicago
Du, Y., Kong, C., Zhu, Y., Yu, M., Li, Z., Bi, J., Li, Z., Liu, X., Zhang, Z., Yu, X."[Corrigendum] Knockdown of SNHG15 suppresses renal cell carcinoma proliferation and EMT by regulating the NF‑κB signaling pathway". International Journal of Oncology 60, no. 4 (2022): 36. https://doi.org/10.3892/ijo.2022.5326
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