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Hispidulin exhibits potent anticancer activity in vitro and in vivo through activating ER stress in non‑small‑cell lung cancer cells

  • Authors:
    • Li Lv
    • Wenhui Zhang
    • Tingting Li
    • Lifeng Jiang
    • Xinyan Lu
    • Jie Lin
  • View Affiliations / Copyright

    Affiliations: Department of Medical Oncology, The Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan 650101, P.R. China
    Copyright: © Lv et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 1995-2003
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    Published online on: March 30, 2020
       https://doi.org/10.3892/or.2020.7568
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Abstract

Hispidulin is a medicinal natural compound isolated from S. involucrata, which exhibits potent anticancer properties. However, there are few reports on its effects on lung cancer cells. Therefore, the current study investigated the effects of hispidulin on cell viability and apoptosis in human non‑small‑cell lung cancer (NSCLC) cell lines NCI‑H460 and A549 in vitro and in vivo. Methyl thiazolyl tetrazolium, colony formation assay, Hoechst 33342 staining, flow cytometry and western blotting were performed on Human NCI‑H460 and A549 cells. A mouse xenograft model was also established using NCI‑H460 cells. The results showed that the growth of NCI‑H460 and A549 cells was inhibited, while apoptosis was promoted by hispidulin via increased generation of reactive oxygen species (ROS) in a dose‑dependent manner. Furthermore, hispidulin triggered apoptosis in NSCLC cells through upregulating the expression of cleaved caspase‑3 and cleaved poly [ADP‑ribose] polymerase. All these effects were reversed upon pretreatment with glutathione, a selective ROS inhibitor. In addition, endoplasmic reticulum stress (ER stress) in NCI‑H460 cells was activated by hispidulin. Pretreatment with tauroursodeoxycholic acid, a specific ER stress inhibitor, effectively reduced the cell apoptosis induced by hispidulin. In conclusion, hispidulin induces ROS‑mediated apoptosis via activating the ER stress pathway. The current study provides theoretical basis for the antitumor effect of hispidulin in NSCLC.
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Copy and paste a formatted citation
Spandidos Publications style
Lv L, Zhang W, Li T, Jiang L, Lu X and Lin J: Hispidulin exhibits potent anticancer activity in vitro and in vivo through activating ER stress in non‑small‑cell lung cancer cells. Oncol Rep 43: 1995-2003, 2020.
APA
Lv, L., Zhang, W., Li, T., Jiang, L., Lu, X., & Lin, J. (2020). Hispidulin exhibits potent anticancer activity in vitro and in vivo through activating ER stress in non‑small‑cell lung cancer cells. Oncology Reports, 43, 1995-2003. https://doi.org/10.3892/or.2020.7568
MLA
Lv, L., Zhang, W., Li, T., Jiang, L., Lu, X., Lin, J."Hispidulin exhibits potent anticancer activity in vitro and in vivo through activating ER stress in non‑small‑cell lung cancer cells". Oncology Reports 43.6 (2020): 1995-2003.
Chicago
Lv, L., Zhang, W., Li, T., Jiang, L., Lu, X., Lin, J."Hispidulin exhibits potent anticancer activity in vitro and in vivo through activating ER stress in non‑small‑cell lung cancer cells". Oncology Reports 43, no. 6 (2020): 1995-2003. https://doi.org/10.3892/or.2020.7568
Copy and paste a formatted citation
x
Spandidos Publications style
Lv L, Zhang W, Li T, Jiang L, Lu X and Lin J: Hispidulin exhibits potent anticancer activity in vitro and in vivo through activating ER stress in non‑small‑cell lung cancer cells. Oncol Rep 43: 1995-2003, 2020.
APA
Lv, L., Zhang, W., Li, T., Jiang, L., Lu, X., & Lin, J. (2020). Hispidulin exhibits potent anticancer activity in vitro and in vivo through activating ER stress in non‑small‑cell lung cancer cells. Oncology Reports, 43, 1995-2003. https://doi.org/10.3892/or.2020.7568
MLA
Lv, L., Zhang, W., Li, T., Jiang, L., Lu, X., Lin, J."Hispidulin exhibits potent anticancer activity in vitro and in vivo through activating ER stress in non‑small‑cell lung cancer cells". Oncology Reports 43.6 (2020): 1995-2003.
Chicago
Lv, L., Zhang, W., Li, T., Jiang, L., Lu, X., Lin, J."Hispidulin exhibits potent anticancer activity in vitro and in vivo through activating ER stress in non‑small‑cell lung cancer cells". Oncology Reports 43, no. 6 (2020): 1995-2003. https://doi.org/10.3892/or.2020.7568
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