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Article

MicroRNA‑145 sensitizes cervical cancer cells to low‑dose irradiation by downregulating OCT4 expression

  • Authors:
    • Siqi Yan
    • Xiangjun Li
    • Qiao Jin
    • Jun Yuan
  • View Affiliations / Copyright

    Affiliations: Department of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, P.R. China, Department of Oncology, The Second People's Hospital, Changsha, Hunan 410000, P.R. China, Department of Oncology, Third Xiangya Hospital, Central South University, Changsha, Hunan 410013, P.R. China
  • Pages: 3130-3136
    |
    Published online on: September 20, 2016
       https://doi.org/10.3892/etm.2016.3731
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Abstract

Poor elucidation of the mechanisms involved in regulating the radiosensitivity of cancers prevents the extensive application of low‑dose radiotherapy in clinical settings. The present study was conducted to investigate the role of microRNA‑145 (miR‑145) in the modulation of cervical cancer cell radiosensitivity, as well as to identify the underlying target of miR‑145 during this process. Cervical cancer tera cells were initially exposed to doses of radiation between 1 and 6 Gy before the assessments of the cell viability and apoptosis rate. Irradiation at dose of 1 Gy was screened as optimum dose and used in subsequent experiments. A dual luciferase reporter assay was performed to demonstrate that octamer‑binding transcription factor 4 (OCT4) is a target of miR‑145 in cervical cancer. Consequently, OCT4 was suggested to be a target of miR‑145, as a dual luciferase vector that was ligated to a fragment corresponding to the predicted target site of miR‑145 in OCT4 3'‑UTR showed an 83% reduction in fluorescence. Following exposure to 1 Gy irradiation, tera cells transfected with miR‑145 mimics, which showed downregulation of OCT4 and cyclin D1, had lower cell viability and cell migration rate and higher apoptosis rate compared to non‑transfected cells. However, the co‑transfection of miR‑145 mimics and OCT4 expression vector restored OCT4 and cyclin D1 expression levels and made no significant difference in terms of cell viability, cell migration rate and apoptosis rate. The present results indicate that miR‑145 increases the radiosensitivity of cervical cancer cells by silencing OCT4, that cyclin D1 is putatively under the positive regulation of OCT4 and mediates miR‑145 function.
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Copy and paste a formatted citation
Spandidos Publications style
Yan S, Li X, Jin Q and Yuan J: MicroRNA‑145 sensitizes cervical cancer cells to low‑dose irradiation by downregulating OCT4 expression. Exp Ther Med 12: 3130-3136, 2016.
APA
Yan, S., Li, X., Jin, Q., & Yuan, J. (2016). MicroRNA‑145 sensitizes cervical cancer cells to low‑dose irradiation by downregulating OCT4 expression. Experimental and Therapeutic Medicine, 12, 3130-3136. https://doi.org/10.3892/etm.2016.3731
MLA
Yan, S., Li, X., Jin, Q., Yuan, J."MicroRNA‑145 sensitizes cervical cancer cells to low‑dose irradiation by downregulating OCT4 expression". Experimental and Therapeutic Medicine 12.5 (2016): 3130-3136.
Chicago
Yan, S., Li, X., Jin, Q., Yuan, J."MicroRNA‑145 sensitizes cervical cancer cells to low‑dose irradiation by downregulating OCT4 expression". Experimental and Therapeutic Medicine 12, no. 5 (2016): 3130-3136. https://doi.org/10.3892/etm.2016.3731
Copy and paste a formatted citation
x
Spandidos Publications style
Yan S, Li X, Jin Q and Yuan J: MicroRNA‑145 sensitizes cervical cancer cells to low‑dose irradiation by downregulating OCT4 expression. Exp Ther Med 12: 3130-3136, 2016.
APA
Yan, S., Li, X., Jin, Q., & Yuan, J. (2016). MicroRNA‑145 sensitizes cervical cancer cells to low‑dose irradiation by downregulating OCT4 expression. Experimental and Therapeutic Medicine, 12, 3130-3136. https://doi.org/10.3892/etm.2016.3731
MLA
Yan, S., Li, X., Jin, Q., Yuan, J."MicroRNA‑145 sensitizes cervical cancer cells to low‑dose irradiation by downregulating OCT4 expression". Experimental and Therapeutic Medicine 12.5 (2016): 3130-3136.
Chicago
Yan, S., Li, X., Jin, Q., Yuan, J."MicroRNA‑145 sensitizes cervical cancer cells to low‑dose irradiation by downregulating OCT4 expression". Experimental and Therapeutic Medicine 12, no. 5 (2016): 3130-3136. https://doi.org/10.3892/etm.2016.3731
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