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Article

Wogonin induces apoptosis and endoplasmic reticulum stress in HL-60 leukemia cells through inhibition of the PI3K-AKT signaling pathway

  • Authors:
    • Chengjun Hu
    • Maozhong Xu
    • Rujuan Qin
    • Weifeng Chen
    • Xin Xu
  • View Affiliations / Copyright

    Affiliations: Department of Hematology, The Affiliated Jiangyin Hospital of Southeast University Medical College, Jiangyin, Jiangsu 214400, P.R. China
  • Pages: 3146-3154
    |
    Published online on: April 2, 2015
       https://doi.org/10.3892/or.2015.3896
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Abstract

Wogonin is a flavonoid isolated from Scutellaria baicalensis root and has multiple pharmacological effects, including anticancer effects. Recent studies have shown that wogonin induces cell cycle arrest and reverses multi‑drug resistance in the human K562 leukemia cell line. However, its pharmacological function in the apoptosis of leukemia cells remains unknown. Therefore, we hypothesized that wogonin can induce apoptosis in the HL-60 leukemia cell line. In the present study, the HL-60 cells were treated with different doses of wogonin (0-150 µM). Wogonin inhibited the viability of HL-60 cells in a dose-dependent and time‑dependent manner. Flow cytometry and analyses of caspase and PARP-1 activation and the Bax/Bcl-2 ratio, demonstrated that the cytotoxic effect of wogonin on HL-60 cells was mediated by caspase‑dependent and mitochondrial-dependent apoptosis. Wogonin also induced the expression of certain members of the endoplasmic reticulum (ER) stress pathway (CHOP, GRP94 and GRP78) and the activation of multiple branches of ER stress transducers (IRE1α, PERK-eIF2α and ATF6) in the HL-60 cells. In addition, wogonin reduced the phosphorylation of PI3K and AKT in the HL-60 cells. Furthermore, constitutive activation of AKT induced by adenoviral vectors inhibited the pro-apoptotic effects and ER stress induced by wogonin in the HL-60 cells. In summary, our results indicated that wogonin induced apoptosis and ER stress in HL-60 cells, which was mediated by the inhibition of the PI3K-AKT signaling pathway.
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Copy and paste a formatted citation
Spandidos Publications style
Hu C, Xu M, Qin R, Chen W and Xu X: Wogonin induces apoptosis and endoplasmic reticulum stress in HL-60 leukemia cells through inhibition of the PI3K-AKT signaling pathway. Oncol Rep 33: 3146-3154, 2015.
APA
Hu, C., Xu, M., Qin, R., Chen, W., & Xu, X. (2015). Wogonin induces apoptosis and endoplasmic reticulum stress in HL-60 leukemia cells through inhibition of the PI3K-AKT signaling pathway. Oncology Reports, 33, 3146-3154. https://doi.org/10.3892/or.2015.3896
MLA
Hu, C., Xu, M., Qin, R., Chen, W., Xu, X."Wogonin induces apoptosis and endoplasmic reticulum stress in HL-60 leukemia cells through inhibition of the PI3K-AKT signaling pathway". Oncology Reports 33.6 (2015): 3146-3154.
Chicago
Hu, C., Xu, M., Qin, R., Chen, W., Xu, X."Wogonin induces apoptosis and endoplasmic reticulum stress in HL-60 leukemia cells through inhibition of the PI3K-AKT signaling pathway". Oncology Reports 33, no. 6 (2015): 3146-3154. https://doi.org/10.3892/or.2015.3896
Copy and paste a formatted citation
x
Spandidos Publications style
Hu C, Xu M, Qin R, Chen W and Xu X: Wogonin induces apoptosis and endoplasmic reticulum stress in HL-60 leukemia cells through inhibition of the PI3K-AKT signaling pathway. Oncol Rep 33: 3146-3154, 2015.
APA
Hu, C., Xu, M., Qin, R., Chen, W., & Xu, X. (2015). Wogonin induces apoptosis and endoplasmic reticulum stress in HL-60 leukemia cells through inhibition of the PI3K-AKT signaling pathway. Oncology Reports, 33, 3146-3154. https://doi.org/10.3892/or.2015.3896
MLA
Hu, C., Xu, M., Qin, R., Chen, W., Xu, X."Wogonin induces apoptosis and endoplasmic reticulum stress in HL-60 leukemia cells through inhibition of the PI3K-AKT signaling pathway". Oncology Reports 33.6 (2015): 3146-3154.
Chicago
Hu, C., Xu, M., Qin, R., Chen, W., Xu, X."Wogonin induces apoptosis and endoplasmic reticulum stress in HL-60 leukemia cells through inhibition of the PI3K-AKT signaling pathway". Oncology Reports 33, no. 6 (2015): 3146-3154. https://doi.org/10.3892/or.2015.3896
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