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Oncology Reports
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Print ISSN: 1021-335X Online ISSN: 1791-2431
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May-2024 Volume 51 Issue 5

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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.

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

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

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

Experimental and Therapeutic Medicine

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

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

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

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

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

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Correction Open Access

[Corrigendum] Induction of microRNA‑let‑7a inhibits lung adeno­carcinoma cell growth by regulating cyclin D1

  • Authors:
    • Wei Zhao
    • Jin-Xia Hu
    • Rui-Min Hao
    • Qian Zhang
    • Jun-Qi Guo
    • You-Jie Li
    • Ning Xie
    • Lu-Ying Liu
    • Ping-Yu Wang
    • Can Zhang
    • Shu-Yang Xie
  • View Affiliations / Copyright

    Affiliations: Key Laboratory of Tumor Molecular Biology in Binzhou Medical University, Department of Biochemistry and Molecular Biology, Binzhou Medical University, YanTai, Shandong 264003, P.R. China, Department of Chest Surgery, YanTaiShan Hospital, YanTai, Shandong 264000, P.R. China, Department of Pathology, Binzhou Medical University, YanTai, Shandong 264003, P.R. China, Genetics and Aging Research Unit, Mass General Institute for Neurodegenerative Diseases (MIND), Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA 02129‑2060, USA
    Copyright: © Zhao et al. This is an open access article distributed under the terms of Creative Commons Attribution License [CC BY 4.0].
  • Article Number: 62
    |
    Published online on: March 5, 2024
       https://doi.org/10.3892/or.2024.8721
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Article

Oncol Rep 40: [Related article:] 1843–1854, 2018; DOI: 10.3892/or.2018.6593

After the publication of the article, an interested reader drew to the authors' attention that, in the western blots shown in Fig. 5C and D, a pair of data panels were inadvertently duplicated comparing between panels (C) and (D); in addition, the cell migration data shown in Fig. 7F on p. 1852 were selected incorrectly.

Figure 5.

The effects of let-7a on cell apoptosis and gene expression. (A) Cell apoptosis in A549 cells was determined by flow cytometry. *P<0.05. (B) The effects of let-7a on apoptosis were analyzed in H1299 cells. *P<0.05. (C) Let-7a significantly downregulated Bcl-2 expression and upregulated the expression of Bax, cleaved-caspase-3, −8 and −9, compared with the scrambled control treatment in A549 cells. The let-7a-inhibitor increased the Bcl-2 levels and reduced Bax, and decreased cleaved-caspase-3, −8 and −9. (D) The expression of Bcl-2, Bax and cleaved-caspase-3, −8 and −9 was detected in the H1299 cell line. GAPDH was used as an internal control.

Figure 7.

Continued. Let-7a suppresses cancer cell migration. (E and F) Let-7a inhibitor improved cell migration ability, which was reversed by cyclin D1-siRNA in A549 and H1299 cell lines. *P<0.01. (G and H) Cell invasion ability was improved by let-7a-inhibitor, which was reversed by cyclin D1-siRNA in A549 and H1299 cell lines. *P<0.01.

The authors have examined their original data, and realize that these errors arose inadvertently as a consequence of their mishandling of their data. The revised versions of Figs. 5 and 7, featuring the corrected data for the caspase-8 experiment in Fig. 5C and alternative data for the cell migration assay experiments in Fig. 7F, are shown on the next two pages. The revised data shown for these Figures do not affect the overall conclusions reported in the paper. All the authors agree to the publication of this corrigendum, and are grateful to the Editor of Oncology Reports for allowing them the opportunity to publish this. Furthermore, the authors apologize to the readership for any inconvenience caused.

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Copy and paste a formatted citation
Spandidos Publications style
Zhao W, Hu J, Hao R, Zhang Q, Guo J, Li Y, Xie N, Liu L, Wang P, Zhang C, Zhang C, et al: [Corrigendum] Induction of microRNA‑let‑7a inhibits lung adeno­carcinoma cell growth by regulating cyclin D1. Oncol Rep 51: 62, 2024.
APA
Zhao, W., Hu, J., Hao, R., Zhang, Q., Guo, J., Li, Y. ... Xie, S. (2024). [Corrigendum] Induction of microRNA‑let‑7a inhibits lung adeno­carcinoma cell growth by regulating cyclin D1. Oncology Reports, 51, 62. https://doi.org/10.3892/or.2024.8721
MLA
Zhao, W., Hu, J., Hao, R., Zhang, Q., Guo, J., Li, Y., Xie, N., Liu, L., Wang, P., Zhang, C., Xie, S."[Corrigendum] Induction of microRNA‑let‑7a inhibits lung adeno­carcinoma cell growth by regulating cyclin D1". Oncology Reports 51.5 (2024): 62.
Chicago
Zhao, W., Hu, J., Hao, R., Zhang, Q., Guo, J., Li, Y., Xie, N., Liu, L., Wang, P., Zhang, C., Xie, S."[Corrigendum] Induction of microRNA‑let‑7a inhibits lung adeno­carcinoma cell growth by regulating cyclin D1". Oncology Reports 51, no. 5 (2024): 62. https://doi.org/10.3892/or.2024.8721
Copy and paste a formatted citation
x
Spandidos Publications style
Zhao W, Hu J, Hao R, Zhang Q, Guo J, Li Y, Xie N, Liu L, Wang P, Zhang C, Zhang C, et al: [Corrigendum] Induction of microRNA‑let‑7a inhibits lung adeno­carcinoma cell growth by regulating cyclin D1. Oncol Rep 51: 62, 2024.
APA
Zhao, W., Hu, J., Hao, R., Zhang, Q., Guo, J., Li, Y. ... Xie, S. (2024). [Corrigendum] Induction of microRNA‑let‑7a inhibits lung adeno­carcinoma cell growth by regulating cyclin D1. Oncology Reports, 51, 62. https://doi.org/10.3892/or.2024.8721
MLA
Zhao, W., Hu, J., Hao, R., Zhang, Q., Guo, J., Li, Y., Xie, N., Liu, L., Wang, P., Zhang, C., Xie, S."[Corrigendum] Induction of microRNA‑let‑7a inhibits lung adeno­carcinoma cell growth by regulating cyclin D1". Oncology Reports 51.5 (2024): 62.
Chicago
Zhao, W., Hu, J., Hao, R., Zhang, Q., Guo, J., Li, Y., Xie, N., Liu, L., Wang, P., Zhang, C., Xie, S."[Corrigendum] Induction of microRNA‑let‑7a inhibits lung adeno­carcinoma cell growth by regulating cyclin D1". Oncology Reports 51, no. 5 (2024): 62. https://doi.org/10.3892/or.2024.8721
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