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Article

MicroRNA‑10a enhances the metastatic potential of cervical cancer cells by targeting phosphatase and tensin homologue

  • Authors:
    • Tianhe Zeng
    • Guiling Li
  • View Affiliations / Copyright

    Affiliations: Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430023, P.R. China
  • Pages: 1377-1382
    |
    Published online on: July 9, 2014
       https://doi.org/10.3892/mmr.2014.2370
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Abstract

Cervical cancer is one of the leading causes of cancer‑related mortality worldwide. Previously, the upregulation of microRNA (miR)‑10a has been identified in human cervical cancer. The present study firstly demonstrated that miR‑10a was markedly upregulated in primary tumor tissues in patients with positive lymph node metastasis (LN+) compared with negative (LN‑) by quantitative polymerase chain reaction. miR‑10a mimics markedly enhanced cervical cancer cell migration and invasion abilities, and accordingly the miR‑10a inhibitor suppressed those functions. Furthermore, these data suggested that the phosphatase and tensin homologue (PTEN) was inhibited by miR‑10a through an miR‑10a binding site within the 3'‑untranslated region of PTEN at the posttranscriptional level, and that miR‑10a mimics promoted nuclear translocation of β‑catenin. Therefore, it was concluded that the overexpression of miR‑10a contributes to metastasis in cervical cancer by targeting PTEN. miR‑10a may therefore be used clinically as a molecular marker for patients with cervical cancer lymph node metastasis.
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Copy and paste a formatted citation
Spandidos Publications style
Zeng T and Li G: MicroRNA‑10a enhances the metastatic potential of cervical cancer cells by targeting phosphatase and tensin homologue. Mol Med Rep 10: 1377-1382, 2014.
APA
Zeng, T., & Li, G. (2014). MicroRNA‑10a enhances the metastatic potential of cervical cancer cells by targeting phosphatase and tensin homologue. Molecular Medicine Reports, 10, 1377-1382. https://doi.org/10.3892/mmr.2014.2370
MLA
Zeng, T., Li, G."MicroRNA‑10a enhances the metastatic potential of cervical cancer cells by targeting phosphatase and tensin homologue". Molecular Medicine Reports 10.3 (2014): 1377-1382.
Chicago
Zeng, T., Li, G."MicroRNA‑10a enhances the metastatic potential of cervical cancer cells by targeting phosphatase and tensin homologue". Molecular Medicine Reports 10, no. 3 (2014): 1377-1382. https://doi.org/10.3892/mmr.2014.2370
Copy and paste a formatted citation
x
Spandidos Publications style
Zeng T and Li G: MicroRNA‑10a enhances the metastatic potential of cervical cancer cells by targeting phosphatase and tensin homologue. Mol Med Rep 10: 1377-1382, 2014.
APA
Zeng, T., & Li, G. (2014). MicroRNA‑10a enhances the metastatic potential of cervical cancer cells by targeting phosphatase and tensin homologue. Molecular Medicine Reports, 10, 1377-1382. https://doi.org/10.3892/mmr.2014.2370
MLA
Zeng, T., Li, G."MicroRNA‑10a enhances the metastatic potential of cervical cancer cells by targeting phosphatase and tensin homologue". Molecular Medicine Reports 10.3 (2014): 1377-1382.
Chicago
Zeng, T., Li, G."MicroRNA‑10a enhances the metastatic potential of cervical cancer cells by targeting phosphatase and tensin homologue". Molecular Medicine Reports 10, no. 3 (2014): 1377-1382. https://doi.org/10.3892/mmr.2014.2370
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