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miR-183 modulated cell proliferation and apoptosis in ovarian cancer through the TGF-β/Smad4 signaling pathway

  • Authors:
    • Junhui Zhou
    • Caixia Zhang
    • Bo Zhou
    • Daqiong Jiang
  • View Affiliations / Copyright

    Affiliations: Department of Nursing, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, P.R. China, Department of Gynecological Oncology, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, P.R. China
    Copyright: © Zhou et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 1734-1746
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    Published online on: January 29, 2019
       https://doi.org/10.3892/ijmm.2019.4082
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Abstract

An increasing body of evidence has revealed that the aberrant expression of microRNAs (miRNAs/miRs) is involved in the development and progression of ovarian cancer (OC). miR‑183 has been demonstrated to act as a tumor suppressor and oncogene in various types of human cancers. However, the biological role of miR‑183 in OC still remains unclear. The aim of the present study was to investigate the role of miR‑183 and evaluate its underlying mechanism in OC. In the present study, miR‑183 was observed to be upregulated in OC tissues and cell lines as determined by reverse transcription‑quantitative polymerase chain reaction. The effects of miR‑183 on OC were further investigated via western blotting, MTT, wound healing, Transwell and immunofluorescence analyses. Downregulation of miR‑183 markedly inhibited cell proliferation, migration and invasion, and promoted apoptosis in OC cells. Furthermore, it was initially confirmed that mothers against decapentaplegic homolog 4 (Smad4) was identified as an efficient target of miR‑183 by luciferase activity assay. Finally, the results revealed that miR‑183 directly regulated biological function via the transforming growth factor (TGF)‑β/Smad4 signaling pathway in OC cells. In conclusion, the results of the present study suggested that miR‑183 exerted tumor‑promoting roles in OC, at least partially by regulating Smad4 via the TGF‑β/Smad4 signaling pathway. Therefore, miR‑183 may serve as a potential target for the diagnosis and prognosis of OC.
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Copy and paste a formatted citation
Spandidos Publications style
Zhou J, Zhang C, Zhou B and Jiang D: miR-183 modulated cell proliferation and apoptosis in ovarian cancer through the TGF-β/Smad4 signaling pathway. Int J Mol Med 43: 1734-1746, 2019.
APA
Zhou, J., Zhang, C., Zhou, B., & Jiang, D. (2019). miR-183 modulated cell proliferation and apoptosis in ovarian cancer through the TGF-β/Smad4 signaling pathway. International Journal of Molecular Medicine, 43, 1734-1746. https://doi.org/10.3892/ijmm.2019.4082
MLA
Zhou, J., Zhang, C., Zhou, B., Jiang, D."miR-183 modulated cell proliferation and apoptosis in ovarian cancer through the TGF-β/Smad4 signaling pathway". International Journal of Molecular Medicine 43.4 (2019): 1734-1746.
Chicago
Zhou, J., Zhang, C., Zhou, B., Jiang, D."miR-183 modulated cell proliferation and apoptosis in ovarian cancer through the TGF-β/Smad4 signaling pathway". International Journal of Molecular Medicine 43, no. 4 (2019): 1734-1746. https://doi.org/10.3892/ijmm.2019.4082
Copy and paste a formatted citation
x
Spandidos Publications style
Zhou J, Zhang C, Zhou B and Jiang D: miR-183 modulated cell proliferation and apoptosis in ovarian cancer through the TGF-β/Smad4 signaling pathway. Int J Mol Med 43: 1734-1746, 2019.
APA
Zhou, J., Zhang, C., Zhou, B., & Jiang, D. (2019). miR-183 modulated cell proliferation and apoptosis in ovarian cancer through the TGF-β/Smad4 signaling pathway. International Journal of Molecular Medicine, 43, 1734-1746. https://doi.org/10.3892/ijmm.2019.4082
MLA
Zhou, J., Zhang, C., Zhou, B., Jiang, D."miR-183 modulated cell proliferation and apoptosis in ovarian cancer through the TGF-β/Smad4 signaling pathway". International Journal of Molecular Medicine 43.4 (2019): 1734-1746.
Chicago
Zhou, J., Zhang, C., Zhou, B., Jiang, D."miR-183 modulated cell proliferation and apoptosis in ovarian cancer through the TGF-β/Smad4 signaling pathway". International Journal of Molecular Medicine 43, no. 4 (2019): 1734-1746. https://doi.org/10.3892/ijmm.2019.4082
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