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MicroRNA-372 functions as a tumor suppressor in cell invasion, migration and epithelial-mesenchymal transition by targeting ATAD2 in renal cell carcinoma

  • Authors:
    • Shiqi Ji
    • Xiaolin Su
    • Haijian Zhang
    • Zhixing Han
    • Yuqian Zhao
    • Qingjun Liu
  • View Affiliations / Copyright

    Affiliations: Department of Urology, Beijing Ditan Hospital Capital Medical University, Capital Medical University, Beijing 100015, P.R. China, Department of Emergency, Beijing First Hospital of Integrated Chinese and Western Medicine, Beijing 100021, P.R. China
  • Pages: 2400-2408
    |
    Published online on: December 28, 2018
       https://doi.org/10.3892/ol.2018.9871
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Abstract

In recent years, renal cell carcinoma (RCC) has exhibited an increasing incidence and mortality rate worldwide. Accumulating evidence has identified that microRNAs (miRNAs) function as negative or positive regulators of many malignant tumors; however, the roles of miR-372 in RCC remain unclear. The focus of the present study was the functions of miR-372 in RCC metastasis and EMT. Data revealed that miR-372 expression levels were significantly downregulated in RCC tissue samples and cells. Moreover, the decreased expression levels were strongly associated with the poor survival rates and adverse clinical characteristics of RCC patients. Accordingly, miR-372 overexpression markedly inhibited RCC cell invasion, migration and EMT. In terms of the potential mechanisms, ATAD2, the expression of which was inversely correlated with miR-372 expression in RCC, was identified as a direct functional target of miR-372. Notably, ATAD2 silence exerted suppressive functions in RCC cells, being similar to the effects of miR-372 overexpression. In conclusion, findings of this study indicate that miR-372 repressed RCC EMT and metastasis via targeting ATAD2, suggesting that the miR-372/ATAD2 axis may be therapeutic biomarkers for RCC.
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Copy and paste a formatted citation
Spandidos Publications style
Ji S, Su X, Zhang H, Han Z, Zhao Y and Liu Q: MicroRNA-372 functions as a tumor suppressor in cell invasion, migration and epithelial-mesenchymal transition by targeting ATAD2 in renal cell carcinoma. Oncol Lett 17: 2400-2408, 2019.
APA
Ji, S., Su, X., Zhang, H., Han, Z., Zhao, Y., & Liu, Q. (2019). MicroRNA-372 functions as a tumor suppressor in cell invasion, migration and epithelial-mesenchymal transition by targeting ATAD2 in renal cell carcinoma. Oncology Letters, 17, 2400-2408. https://doi.org/10.3892/ol.2018.9871
MLA
Ji, S., Su, X., Zhang, H., Han, Z., Zhao, Y., Liu, Q."MicroRNA-372 functions as a tumor suppressor in cell invasion, migration and epithelial-mesenchymal transition by targeting ATAD2 in renal cell carcinoma". Oncology Letters 17.2 (2019): 2400-2408.
Chicago
Ji, S., Su, X., Zhang, H., Han, Z., Zhao, Y., Liu, Q."MicroRNA-372 functions as a tumor suppressor in cell invasion, migration and epithelial-mesenchymal transition by targeting ATAD2 in renal cell carcinoma". Oncology Letters 17, no. 2 (2019): 2400-2408. https://doi.org/10.3892/ol.2018.9871
Copy and paste a formatted citation
x
Spandidos Publications style
Ji S, Su X, Zhang H, Han Z, Zhao Y and Liu Q: MicroRNA-372 functions as a tumor suppressor in cell invasion, migration and epithelial-mesenchymal transition by targeting ATAD2 in renal cell carcinoma. Oncol Lett 17: 2400-2408, 2019.
APA
Ji, S., Su, X., Zhang, H., Han, Z., Zhao, Y., & Liu, Q. (2019). MicroRNA-372 functions as a tumor suppressor in cell invasion, migration and epithelial-mesenchymal transition by targeting ATAD2 in renal cell carcinoma. Oncology Letters, 17, 2400-2408. https://doi.org/10.3892/ol.2018.9871
MLA
Ji, S., Su, X., Zhang, H., Han, Z., Zhao, Y., Liu, Q."MicroRNA-372 functions as a tumor suppressor in cell invasion, migration and epithelial-mesenchymal transition by targeting ATAD2 in renal cell carcinoma". Oncology Letters 17.2 (2019): 2400-2408.
Chicago
Ji, S., Su, X., Zhang, H., Han, Z., Zhao, Y., Liu, Q."MicroRNA-372 functions as a tumor suppressor in cell invasion, migration and epithelial-mesenchymal transition by targeting ATAD2 in renal cell carcinoma". Oncology Letters 17, no. 2 (2019): 2400-2408. https://doi.org/10.3892/ol.2018.9871
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