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Oridonin induces apoptosis in HGC‑27 cells by activating the JNK signaling pathway

  • Authors:
    • Dong‑Lin Ren
    • Roshan Ara Ghoorun
    • Xiao‑Hua Wu
    • Hong‑Lei Chen
    • Qian Zhou
    • Xiao‑Bin Wu
  • View Affiliations / Copyright

    Affiliations: Department of Colorectal Surgery, The Sixth Affiliated Hospital of Sun Yat‑sen University, Guangzhou, Guangdong 510655, P.R. China, Department of Oncology, Longhu People's Hospital, Shantou, Guangdong 515000, P.R. China, Department of Endoscopy, The Eighth Affiliated Hospital of Sun Yat‑sen University, Shenzhen, Guangdong 518033, P.R. China, Department of Gastrointestinal Surgery, The Eighth Affiliated Hospital of Sun Yat‑sen University, Shenzhen, Guangdong 518033, P.R. China
    Copyright: © Ren et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 255-260
    |
    Published online on: November 14, 2019
       https://doi.org/10.3892/ol.2019.11104
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Abstract

Gastric cancer (GC) is a very common type of cancer. Although current treatment modalities include surgical resection and chemotherapy, many patients are either not eligible for radical resection or have a poor response to chemotherapy. Due to the complex features of the disease, there is a need for complementary therapy. In the present study, the effects of oridonin on cell proliferation, invasion and apoptosis were assessed in the HGC‑27 cell line using the Cell Counting Kit‑8 assay, real‑time cell analysis, and an Annexin V‑FITC/propidium iodide (PI) detection kit, respectively. The effect of oridonin on apoptosis, through the JNK pathway, was also investigated using western blotting. The present study demonstrated that oridonin can suppress cell viability and inhibit cell proliferation by inducing G2/M arrest. Oridonin also induced caspase‑dependent apoptosis in cells by activating the phosphorylated‑JNK/C‑JUN pathway. These results demonstrate the potential of oridonin as a potential therapeutic compound for the treatment of GC.
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Copy and paste a formatted citation
Spandidos Publications style
Ren DL, Ghoorun RA, Wu XH, Chen HL, Zhou Q and Wu XB: Oridonin induces apoptosis in HGC‑27 cells by activating the JNK signaling pathway. Oncol Lett 19: 255-260, 2020.
APA
Ren, D., Ghoorun, R.A., Wu, X., Chen, H., Zhou, Q., & Wu, X. (2020). Oridonin induces apoptosis in HGC‑27 cells by activating the JNK signaling pathway. Oncology Letters, 19, 255-260. https://doi.org/10.3892/ol.2019.11104
MLA
Ren, D., Ghoorun, R. A., Wu, X., Chen, H., Zhou, Q., Wu, X."Oridonin induces apoptosis in HGC‑27 cells by activating the JNK signaling pathway". Oncology Letters 19.1 (2020): 255-260.
Chicago
Ren, D., Ghoorun, R. A., Wu, X., Chen, H., Zhou, Q., Wu, X."Oridonin induces apoptosis in HGC‑27 cells by activating the JNK signaling pathway". Oncology Letters 19, no. 1 (2020): 255-260. https://doi.org/10.3892/ol.2019.11104
Copy and paste a formatted citation
x
Spandidos Publications style
Ren DL, Ghoorun RA, Wu XH, Chen HL, Zhou Q and Wu XB: Oridonin induces apoptosis in HGC‑27 cells by activating the JNK signaling pathway. Oncol Lett 19: 255-260, 2020.
APA
Ren, D., Ghoorun, R.A., Wu, X., Chen, H., Zhou, Q., & Wu, X. (2020). Oridonin induces apoptosis in HGC‑27 cells by activating the JNK signaling pathway. Oncology Letters, 19, 255-260. https://doi.org/10.3892/ol.2019.11104
MLA
Ren, D., Ghoorun, R. A., Wu, X., Chen, H., Zhou, Q., Wu, X."Oridonin induces apoptosis in HGC‑27 cells by activating the JNK signaling pathway". Oncology Letters 19.1 (2020): 255-260.
Chicago
Ren, D., Ghoorun, R. A., Wu, X., Chen, H., Zhou, Q., Wu, X."Oridonin induces apoptosis in HGC‑27 cells by activating the JNK signaling pathway". Oncology Letters 19, no. 1 (2020): 255-260. https://doi.org/10.3892/ol.2019.11104
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