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Prognostic significance of microRNA‑200c in various types of cancer: An updated meta‑analysis of 34 studies

  • Authors:
    • Jia‑Yi Zhang
    • Ya‑Min Wang
    • Le‑Bin Song
    • Chen Chen
    • Yi‑Chun Wang
    • Ning‑Hong Song
  • View Affiliations / Copyright

    Affiliations: Department of Urology, The First Affiliated Hospital with Nanjing Medical University, Nanjing 210029, P.R. China, The First Clinical Medical College of Nanjing Medical University, Nanjing 210029, P.R. China
    Copyright: © Zhang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 933-941
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    Published online on: March 30, 2016
       https://doi.org/10.3892/mco.2016.842
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Abstract

Previous studies have indicated that miR‑200c is a promising cancer biomarker. However, different studies have presented conflicting results. Therefore, the aim of the present study was to perform a meta‑analysis of miR‑200c based on 34 relevant studies. The Materials and methods sections of papers were carefully identified using the databases PubMed, Web of Science and Embase for publications up to December 4, 2015. Pooled hazard ratios (HRs) and 95% confidence intervals (95% CIs) were systematically calculated to investigate the association between the expression of miR‑200c and cancer prognosis. The results demonstrated that elevated expression levels of miR‑200c indicated significantly worse overall survival rates (HR=1.37, 95% CI: 1.01, 1.85), and a high level of miR‑200c was considered an indicator of an unfavorable prognosis in patients from Europe and America (HR=1.85, 95% CI: 1.27, 2.69). Furthermore, overexpression of miR‑200c was significantly associated with progression of the disease in the subgroups of tissue and blood samples (HR=0.68 and 2.45, respectively), and inferior overall survival rates for the blood subgroup were revealed (HR=2.21, 95% CI: 1.04, 4.72). In addition, miR‑200c was of prognostic value in several disease subgroups. Taken together, high expression levels of miR‑200c are of significant prognostic value in various human malignancies.
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Copy and paste a formatted citation
Spandidos Publications style
Zhang JY, Wang YM, Song LB, Chen C, Wang YC and Song NH: Prognostic significance of microRNA‑200c in various types of cancer: An updated meta‑analysis of 34 studies. Mol Clin Oncol 4: 933-941, 2016.
APA
Zhang, J., Wang, Y., Song, L., Chen, C., Wang, Y., & Song, N. (2016). Prognostic significance of microRNA‑200c in various types of cancer: An updated meta‑analysis of 34 studies. Molecular and Clinical Oncology, 4, 933-941. https://doi.org/10.3892/mco.2016.842
MLA
Zhang, J., Wang, Y., Song, L., Chen, C., Wang, Y., Song, N."Prognostic significance of microRNA‑200c in various types of cancer: An updated meta‑analysis of 34 studies". Molecular and Clinical Oncology 4.6 (2016): 933-941.
Chicago
Zhang, J., Wang, Y., Song, L., Chen, C., Wang, Y., Song, N."Prognostic significance of microRNA‑200c in various types of cancer: An updated meta‑analysis of 34 studies". Molecular and Clinical Oncology 4, no. 6 (2016): 933-941. https://doi.org/10.3892/mco.2016.842
Copy and paste a formatted citation
x
Spandidos Publications style
Zhang JY, Wang YM, Song LB, Chen C, Wang YC and Song NH: Prognostic significance of microRNA‑200c in various types of cancer: An updated meta‑analysis of 34 studies. Mol Clin Oncol 4: 933-941, 2016.
APA
Zhang, J., Wang, Y., Song, L., Chen, C., Wang, Y., & Song, N. (2016). Prognostic significance of microRNA‑200c in various types of cancer: An updated meta‑analysis of 34 studies. Molecular and Clinical Oncology, 4, 933-941. https://doi.org/10.3892/mco.2016.842
MLA
Zhang, J., Wang, Y., Song, L., Chen, C., Wang, Y., Song, N."Prognostic significance of microRNA‑200c in various types of cancer: An updated meta‑analysis of 34 studies". Molecular and Clinical Oncology 4.6 (2016): 933-941.
Chicago
Zhang, J., Wang, Y., Song, L., Chen, C., Wang, Y., Song, N."Prognostic significance of microRNA‑200c in various types of cancer: An updated meta‑analysis of 34 studies". Molecular and Clinical Oncology 4, no. 6 (2016): 933-941. https://doi.org/10.3892/mco.2016.842
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