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Article

miR‑125a is upregulated in cancer stem‑like cells derived from TW01 and is responsible for maintaining stemness by inhibiting p53

  • Authors:
    • Jianjun Chen
    • Hui Ouyang
    • Xuemei An
    • Shixi Liu
  • View Affiliations / Copyright

    Affiliations: Department of E.N.T., The First People's Hospital of Neijiang, Neijiang, Sichuan 641000, P.R. China, Department of Neurology, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan 610000, P.R. China, Department of E.N.T., West China Hospital, Sichuan University, Chengdu, Sichuan 610000, P.R. China
    Copyright: © Chen et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 87-94
    |
    Published online on: October 16, 2018
       https://doi.org/10.3892/ol.2018.9587
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Abstract

microRNA (miR)‑125a and miR‑125b were demonstrated to translationally and transcriptionally inhibit the mRNA level of p53 following the induction of chemo‑reagents in our previous report. As a small subpopulation of nasopharyngeal carcinoma (NPC), cancer stem‑like cells (CSCs) function critically in multi‑malignant behaviors, including tumorigenesis and metastasis; however, the expression pattern and regulatory role of miR‑125a, miR‑125b and p53 in CSCs derived from NPC remain unclear. In order to investigate the potential regulatory role of miR‑125 on p53, firstly CSCs was isolated from TW01 by culturing in serum‑free medium. The stemness of isolated CSCs was examined via self‑renewal capacity and side population assays. Following this, the miR‑125a, miR‑125b and p53 mRNA levels were evaluated via reverse‑transcription quantitative polymerase chain reaction. Following the transfections of wild‑type p53 or p53 without DNA binding activity (p53‑mutR248Q) into TW01 or CSCs, Chromatin Immunoprecipitation (ChIP), and cell cycle analyses using flow cytometry or Cell Counting Kit‑8 assays were performed. Notably, it was determined that miR‑125a was significantly upregulated in CSCs derived from TW01, but not miR‑125b, and the mRNA and protein levels of p53 were downregulated. The transfection of p53 significantly decreased the cell viability and stopped cell cycle at the G0/G1 phases in TW01 and CSCs. The ChIP assay confirmed that the ectopic expression of wild‑type p53 transcriptionally regulates its downstream gene, p21, but not B‑cell lymphoma 2 nor Sco2. Taken together, the results of the present study indicated that p53 regulates CSCs via its DNA binding activity and potentially, in CSCs, miR‑125a regulates the expression of p53, maintaining stemness.
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Copy and paste a formatted citation
Spandidos Publications style
Chen J, Ouyang H, An X and Liu S: miR‑125a is upregulated in cancer stem‑like cells derived from TW01 and is responsible for maintaining stemness by inhibiting p53. Oncol Lett 17: 87-94, 2019.
APA
Chen, J., Ouyang, H., An, X., & Liu, S. (2019). miR‑125a is upregulated in cancer stem‑like cells derived from TW01 and is responsible for maintaining stemness by inhibiting p53. Oncology Letters, 17, 87-94. https://doi.org/10.3892/ol.2018.9587
MLA
Chen, J., Ouyang, H., An, X., Liu, S."miR‑125a is upregulated in cancer stem‑like cells derived from TW01 and is responsible for maintaining stemness by inhibiting p53". Oncology Letters 17.1 (2019): 87-94.
Chicago
Chen, J., Ouyang, H., An, X., Liu, S."miR‑125a is upregulated in cancer stem‑like cells derived from TW01 and is responsible for maintaining stemness by inhibiting p53". Oncology Letters 17, no. 1 (2019): 87-94. https://doi.org/10.3892/ol.2018.9587
Copy and paste a formatted citation
x
Spandidos Publications style
Chen J, Ouyang H, An X and Liu S: miR‑125a is upregulated in cancer stem‑like cells derived from TW01 and is responsible for maintaining stemness by inhibiting p53. Oncol Lett 17: 87-94, 2019.
APA
Chen, J., Ouyang, H., An, X., & Liu, S. (2019). miR‑125a is upregulated in cancer stem‑like cells derived from TW01 and is responsible for maintaining stemness by inhibiting p53. Oncology Letters, 17, 87-94. https://doi.org/10.3892/ol.2018.9587
MLA
Chen, J., Ouyang, H., An, X., Liu, S."miR‑125a is upregulated in cancer stem‑like cells derived from TW01 and is responsible for maintaining stemness by inhibiting p53". Oncology Letters 17.1 (2019): 87-94.
Chicago
Chen, J., Ouyang, H., An, X., Liu, S."miR‑125a is upregulated in cancer stem‑like cells derived from TW01 and is responsible for maintaining stemness by inhibiting p53". Oncology Letters 17, no. 1 (2019): 87-94. https://doi.org/10.3892/ol.2018.9587
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