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Article Open Access

si‑TP73‑AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin

  • Authors:
    • Jianjun Peng
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    Affiliations: Department of Gastrointestinal Surgery, The First Affiliated Hospital of Sun Yat‑Sen University, Guangzhou, Guangdong 510080, P.R. China
    Copyright: © Peng et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 3706-3714
    |
    Published online on: July 10, 2018
       https://doi.org/10.3892/ol.2018.9107
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Abstract

Previous studies have revealed that long noncoding RNAs (lncRNAs) function as crucial regulators in various biological processes, including tumorigenesis. Although the expression of lncRNA TP73‑antisense RNA1 (AS1) has been identified in hepatocellular carcinoma and glioma, the biological function of TP73‑AS1 in gastric cancer (GC) remains unclear. Thus, the present study employed a comprehensive analysis on the function of lncRNA TP73‑AS1 in GC. The aim of the present study was to determine the clinical significance and biological function of TP73‑AS1 in human GC tissues and cells. Additionally, the expression of TP73‑AS1 was increased in GC tissues and cell lines and increased expression level of TP73‑AS1 was associated with poor prognosis in patients with GC. Functional assays revealed that silencing of TP73‑AS1 may suppress cell proliferation and enhance the chemotherapeutic response of GC cells to cisplatin through targeting the high mobility group 1/receptor for advanced glycation endproducts signaling pathway. Collectively, the results of the present study demonstrated that TP73‑AS1 may be a novel lncRNA for the clinical prognosis of GC and a potential therapeutic target for the treatment of GC.
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Copy and paste a formatted citation
Spandidos Publications style
Peng J: si‑TP73‑AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin. Oncol Lett 16: 3706-3714, 2018.
APA
Peng, J. (2018). si‑TP73‑AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin. Oncology Letters, 16, 3706-3714. https://doi.org/10.3892/ol.2018.9107
MLA
Peng, J."si‑TP73‑AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin". Oncology Letters 16.3 (2018): 3706-3714.
Chicago
Peng, J."si‑TP73‑AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin". Oncology Letters 16, no. 3 (2018): 3706-3714. https://doi.org/10.3892/ol.2018.9107
Copy and paste a formatted citation
x
Spandidos Publications style
Peng J: si‑TP73‑AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin. Oncol Lett 16: 3706-3714, 2018.
APA
Peng, J. (2018). si‑TP73‑AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin. Oncology Letters, 16, 3706-3714. https://doi.org/10.3892/ol.2018.9107
MLA
Peng, J."si‑TP73‑AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin". Oncology Letters 16.3 (2018): 3706-3714.
Chicago
Peng, J."si‑TP73‑AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin". Oncology Letters 16, no. 3 (2018): 3706-3714. https://doi.org/10.3892/ol.2018.9107
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