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miR‑181d promotes cell proliferation via the IGF1/PI3K/AKT axis in glioma

  • Authors:
    • Dong Tang
    • Wenhong Gao
    • Jian Yang
    • Junhui Liu
    • Jian Zhao
    • Jian Ge
    • Qianxue Chen
    • Baohui Liu
  • View Affiliations / Copyright

    Affiliations: Department of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, Hubei 430060, P.R. China, Department of Neurosurgery, Jingzhou Central Hospital, The Second Clinical Medical College, Yangtze University, Jingzhou, Hubei 434020, P.R. China
    Copyright: © Tang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 3804-3812
    |
    Published online on: August 26, 2020
       https://doi.org/10.3892/mmr.2020.11464
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Abstract

Glioma is a malignant brain cancer that exhibits high invasive ability and poor prognosis. MicroRNA (miR)‑181d has been reported to be involved in the development of glioma. Therefore, the aim of the present study was to investigate whether miR‑181d affected cellular progression by influencing the insulin like growth factor (IGF1)/PI3K/AKT axis. Western blot analysis was performed to analyze the expression levels of specific proteins, and a Cell Counting Kit‑8 assay was used to assess the proliferative ability of cells. Cell cycle progression and cellular apoptosis were both measured using flow cytometry. The results indicated that miR‑181d promoted cellular proliferation and cell cycle progression, while suppressing cellular apoptosis via the IGF1/PI3K/AKT axis. It was demonstrated that the IGF1 and PI3K/AKT inhibitors reversed these observed functions of miR‑181d. Furthermore, miR‑181d enhanced the growth of glioma xenografts in vivo, promoted cell cycle progression and suppressed cellular apoptosis within glioma xenograft tissues. Therefore, this newly identified miR‑181d/IGF1/PI3K/AKT axis may provide novel insights into the pathogenesis of glioma.
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Copy and paste a formatted citation
Spandidos Publications style
Tang D, Gao W, Yang J, Liu J, Zhao J, Ge J, Chen Q and Liu B: miR‑181d promotes cell proliferation via the IGF1/PI3K/AKT axis in glioma. Mol Med Rep 22: 3804-3812, 2020.
APA
Tang, D., Gao, W., Yang, J., Liu, J., Zhao, J., Ge, J. ... Liu, B. (2020). miR‑181d promotes cell proliferation via the IGF1/PI3K/AKT axis in glioma. Molecular Medicine Reports, 22, 3804-3812. https://doi.org/10.3892/mmr.2020.11464
MLA
Tang, D., Gao, W., Yang, J., Liu, J., Zhao, J., Ge, J., Chen, Q., Liu, B."miR‑181d promotes cell proliferation via the IGF1/PI3K/AKT axis in glioma". Molecular Medicine Reports 22.5 (2020): 3804-3812.
Chicago
Tang, D., Gao, W., Yang, J., Liu, J., Zhao, J., Ge, J., Chen, Q., Liu, B."miR‑181d promotes cell proliferation via the IGF1/PI3K/AKT axis in glioma". Molecular Medicine Reports 22, no. 5 (2020): 3804-3812. https://doi.org/10.3892/mmr.2020.11464
Copy and paste a formatted citation
x
Spandidos Publications style
Tang D, Gao W, Yang J, Liu J, Zhao J, Ge J, Chen Q and Liu B: miR‑181d promotes cell proliferation via the IGF1/PI3K/AKT axis in glioma. Mol Med Rep 22: 3804-3812, 2020.
APA
Tang, D., Gao, W., Yang, J., Liu, J., Zhao, J., Ge, J. ... Liu, B. (2020). miR‑181d promotes cell proliferation via the IGF1/PI3K/AKT axis in glioma. Molecular Medicine Reports, 22, 3804-3812. https://doi.org/10.3892/mmr.2020.11464
MLA
Tang, D., Gao, W., Yang, J., Liu, J., Zhao, J., Ge, J., Chen, Q., Liu, B."miR‑181d promotes cell proliferation via the IGF1/PI3K/AKT axis in glioma". Molecular Medicine Reports 22.5 (2020): 3804-3812.
Chicago
Tang, D., Gao, W., Yang, J., Liu, J., Zhao, J., Ge, J., Chen, Q., Liu, B."miR‑181d promotes cell proliferation via the IGF1/PI3K/AKT axis in glioma". Molecular Medicine Reports 22, no. 5 (2020): 3804-3812. https://doi.org/10.3892/mmr.2020.11464
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