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Article Open Access

Knockdown of SNHG12 suppresses tumor metastasis and epithelial‑mesenchymal transition via the Slug/ZEB2 signaling pathway by targeting miR‑218 in NSCLC

  • Authors:
    • Yan Wang
    • Shuxin Liang
    • Yang Yu
    • Yankui Shi
    • Hailiang Zheng
  • View Affiliations / Copyright

    Affiliations: Clinical Laboratory of Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China
    Copyright: © Wang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 2356-2364
    |
    Published online on: December 28, 2018
       https://doi.org/10.3892/ol.2018.9880
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Abstract

Non-small cell lung cancer (NSCLC) is a type of lung cancer which has a high mortality and low survival rate. Previous studies have revealed that long non‑coding RNAs participate in tumorigenesis and metastasis in NSCLC. In the present study, the function of small nucleolar RNA host gene 12 (SNHG12) was investigated in NSCLC. Using reverse transcription‑quantitative polymerase chain reaction analysis, it was identified that SNHG12 was significantly overexpressed in NSCLC specimens. Furthermore, overexpression of SNHG12 was identified to be associated with tumor progression and poor overall survival rates. Knockdown of SNHG12 in NSCLC cells could effectively induce cell apoptosis and suppress cell viability, proliferation, migration and invasion via inhibition of the epithelial‑mesenchymal transition process. Furthermore, a direct interaction between microRNA (miR)‑218 and the binding site of SNHG12 was identified. SNHG12 acted as an endogenous sponge for miR‑218. Knockdown of SNHG12 upregulated the expression level of miR‑218 as well as downregulating the Slug/zinc finger E‑box‑binding homeobox 2 EMT signaling pathway, and thus inhibited cell migration and invasion. Therefore, SNHG12 may serve as a key biomarker and a potential therapeutic target for the treatment of NSCLC.
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Copy and paste a formatted citation
Spandidos Publications style
Wang Y, Liang S, Yu Y, Shi Y and Zheng H: Knockdown of SNHG12 suppresses tumor metastasis and epithelial‑mesenchymal transition via the Slug/ZEB2 signaling pathway by targeting miR‑218 in NSCLC. Oncol Lett 17: 2356-2364, 2019.
APA
Wang, Y., Liang, S., Yu, Y., Shi, Y., & Zheng, H. (2019). Knockdown of SNHG12 suppresses tumor metastasis and epithelial‑mesenchymal transition via the Slug/ZEB2 signaling pathway by targeting miR‑218 in NSCLC. Oncology Letters, 17, 2356-2364. https://doi.org/10.3892/ol.2018.9880
MLA
Wang, Y., Liang, S., Yu, Y., Shi, Y., Zheng, H."Knockdown of SNHG12 suppresses tumor metastasis and epithelial‑mesenchymal transition via the Slug/ZEB2 signaling pathway by targeting miR‑218 in NSCLC". Oncology Letters 17.2 (2019): 2356-2364.
Chicago
Wang, Y., Liang, S., Yu, Y., Shi, Y., Zheng, H."Knockdown of SNHG12 suppresses tumor metastasis and epithelial‑mesenchymal transition via the Slug/ZEB2 signaling pathway by targeting miR‑218 in NSCLC". Oncology Letters 17, no. 2 (2019): 2356-2364. https://doi.org/10.3892/ol.2018.9880
Copy and paste a formatted citation
x
Spandidos Publications style
Wang Y, Liang S, Yu Y, Shi Y and Zheng H: Knockdown of SNHG12 suppresses tumor metastasis and epithelial‑mesenchymal transition via the Slug/ZEB2 signaling pathway by targeting miR‑218 in NSCLC. Oncol Lett 17: 2356-2364, 2019.
APA
Wang, Y., Liang, S., Yu, Y., Shi, Y., & Zheng, H. (2019). Knockdown of SNHG12 suppresses tumor metastasis and epithelial‑mesenchymal transition via the Slug/ZEB2 signaling pathway by targeting miR‑218 in NSCLC. Oncology Letters, 17, 2356-2364. https://doi.org/10.3892/ol.2018.9880
MLA
Wang, Y., Liang, S., Yu, Y., Shi, Y., Zheng, H."Knockdown of SNHG12 suppresses tumor metastasis and epithelial‑mesenchymal transition via the Slug/ZEB2 signaling pathway by targeting miR‑218 in NSCLC". Oncology Letters 17.2 (2019): 2356-2364.
Chicago
Wang, Y., Liang, S., Yu, Y., Shi, Y., Zheng, H."Knockdown of SNHG12 suppresses tumor metastasis and epithelial‑mesenchymal transition via the Slug/ZEB2 signaling pathway by targeting miR‑218 in NSCLC". Oncology Letters 17, no. 2 (2019): 2356-2364. https://doi.org/10.3892/ol.2018.9880
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