Open Access

Effects of downregulated expression of microRNA‑187 in gastric cancer

  • Authors:
    • Wenjing Chen
    • Yongxin Cui
    • Jiulong Wang
    • Yuqing Yuan
    • Xiangwei Sun
    • Liang Zhang
    • Shurong Shen
    • Jun Cheng
  • View Affiliations

  • Published online on: June 15, 2018     https://doi.org/10.3892/etm.2018.6318
  • Pages: 1061-1070
  • Copyright: © Chen et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

microRNAs (miRNAs) are involved in cancer development and progression, and have regulatory roles as tumor suppressors or oncogenes. Although aberrant expression of miR‑187 has been observed in several types of cancer, its pathophysiological role and relevance to tumorigenesis in gastric cancer (GC) remains unknown. In the present study, the expression and biological role of miR‑187 was investigated in 32 specimens of GC tissues and their adjacent non‑tumorigenic controls, and the association between miR‑187 expression and clinical features of GC were analyzed further. Kaplan‑Meier survival curves determined the clinical significance of miR‑187 expression in GC. Following transfection with miR‑187 mimics, the biological functions of miR‑187 were determined by cell proliferation and cell cycle assays. Moreover, following transfection with miR‑187 mimics, the targets regulated by miR‑187 were investigated using western blotting. Luciferase reporter assays confirmed whether miR‑187 regulated MAD2 mitotic arrest deficient‑like 2 (MAD2L2) and stomatin (EPB72)‑like 2 (STOML2) expression. The data of the present study revealed that miR‑187 was significantly downregulated in GC compared with adjacent non‑tumorigenic counterparts. Furthermore, decreased expression of miR‑187 correlated with cell differentiation (P<0.05), TNM staging (P<0.05) and poor prognosis in GC patients. Functional studies indicated that miR‑187 overexpression evidently inhibited MGC‑803 cell proliferation in vitro and altered the cell cycle by arresting cells in the G0/G1 phase. In addition, the luciferase assay and western blotting revealed that MAD2L2 and STOML2 were targeted by miR‑187. In conclusion, it is suggested that miR‑187 functions as a tumor suppressor in GC, and is important in the development and progression of GC. Moreover, miR‑187 may be a potential biomarker and therapeutic target in GC.
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August-2018
Volume 16 Issue 2

Print ISSN: 1792-0981
Online ISSN:1792-1015

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Spandidos Publications style
Chen W, Cui Y, Wang J, Yuan Y, Sun X, Zhang L, Shen S and Cheng J: Effects of downregulated expression of microRNA‑187 in gastric cancer. Exp Ther Med 16: 1061-1070, 2018.
APA
Chen, W., Cui, Y., Wang, J., Yuan, Y., Sun, X., Zhang, L. ... Cheng, J. (2018). Effects of downregulated expression of microRNA‑187 in gastric cancer. Experimental and Therapeutic Medicine, 16, 1061-1070. https://doi.org/10.3892/etm.2018.6318
MLA
Chen, W., Cui, Y., Wang, J., Yuan, Y., Sun, X., Zhang, L., Shen, S., Cheng, J."Effects of downregulated expression of microRNA‑187 in gastric cancer". Experimental and Therapeutic Medicine 16.2 (2018): 1061-1070.
Chicago
Chen, W., Cui, Y., Wang, J., Yuan, Y., Sun, X., Zhang, L., Shen, S., Cheng, J."Effects of downregulated expression of microRNA‑187 in gastric cancer". Experimental and Therapeutic Medicine 16, no. 2 (2018): 1061-1070. https://doi.org/10.3892/etm.2018.6318