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Sinensetin suppresses angiogenesis in liver cancer by targeting the VEGF/VEGFR2/AKT signaling pathway

  • Authors:
    • Xiaο Li
    • Yan Li
    • Yuan Wang
    • Fuhong Liu
    • Yanjun Liu
    • Jiangjiu Liang
    • Rucai Zhan
    • Yue Wu
    • He Ren
    • Xiuyuan Zhang
    • Ju Liu
  • View Affiliations / Copyright

    Affiliations: College of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, Shangdong 250355, P.R. China, Laboratory of Microvascular Medicine, Medical Research Center, The First Affiliated Hospital of Shandong First Medical University and Shandong Provincial Qianfoshan Hospital, Jinan, Shandong 250014, P.R. China, Department of Gerontology, The First Affiliated Hospital of Shandong First Medical University, Jinan, Shandong 250014, P.R. China, Department of Neurosurgery, The First Affiliated Hospital of Shandong First Medical University, Jinan, Shandong 250014, P.R. China
    Copyright: © Li et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Article Number: 360
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    Published online on: March 31, 2022
       https://doi.org/10.3892/etm.2022.11287
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Abstract

Sinensetin (SIN) is a polymethoxy flavone primarily present in citrus fruits. This compound has demonstrated anticancer activity. However, the underlying mechanism of its action has not been fully understood. The present study investigated the impact of SIN on angiogenesis in a liver cancer model. In a murine xenograft tumor model, SIN inhibited the growth of HepG2/C3A human liver hepatoma cell‑derived tumors and reduced the expression levels of platelet/endothelial cell adhesion molecule‑1 and VEGF. In HepG2/C3A cells, SIN repressed VEGF expression by downregulating hypoxia‑inducible factor expression. In cultured human umbilical vein endothelial cells, SIN increased apoptosis and repressed migration and tube formation. In addition, SIN decreased the phosphorylation of VEGFR2 and inhibited the AKT signaling pathway. Molecular docking demonstrated that the VEGFR2 core domain effectively combined with SIN at various important residues. Collectively, these data suggested that SIN inhibited liver cancer angiogenesis by regulating VEGF/VEGFR2/AKT signaling.
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Copy and paste a formatted citation
Spandidos Publications style
Li X, Li Y, Wang Y, Liu F, Liu Y, Liang J, Zhan R, Wu Y, Ren H, Zhang X, Zhang X, et al: Sinensetin suppresses angiogenesis in liver cancer by targeting the VEGF/VEGFR2/AKT signaling pathway. Exp Ther Med 23: 360, 2022.
APA
Li, X., Li, Y., Wang, Y., Liu, F., Liu, Y., Liang, J. ... Liu, J. (2022). Sinensetin suppresses angiogenesis in liver cancer by targeting the VEGF/VEGFR2/AKT signaling pathway. Experimental and Therapeutic Medicine, 23, 360. https://doi.org/10.3892/etm.2022.11287
MLA
Li, X., Li, Y., Wang, Y., Liu, F., Liu, Y., Liang, J., Zhan, R., Wu, Y., Ren, H., Zhang, X., Liu, J."Sinensetin suppresses angiogenesis in liver cancer by targeting the VEGF/VEGFR2/AKT signaling pathway". Experimental and Therapeutic Medicine 23.5 (2022): 360.
Chicago
Li, X., Li, Y., Wang, Y., Liu, F., Liu, Y., Liang, J., Zhan, R., Wu, Y., Ren, H., Zhang, X., Liu, J."Sinensetin suppresses angiogenesis in liver cancer by targeting the VEGF/VEGFR2/AKT signaling pathway". Experimental and Therapeutic Medicine 23, no. 5 (2022): 360. https://doi.org/10.3892/etm.2022.11287
Copy and paste a formatted citation
x
Spandidos Publications style
Li X, Li Y, Wang Y, Liu F, Liu Y, Liang J, Zhan R, Wu Y, Ren H, Zhang X, Zhang X, et al: Sinensetin suppresses angiogenesis in liver cancer by targeting the VEGF/VEGFR2/AKT signaling pathway. Exp Ther Med 23: 360, 2022.
APA
Li, X., Li, Y., Wang, Y., Liu, F., Liu, Y., Liang, J. ... Liu, J. (2022). Sinensetin suppresses angiogenesis in liver cancer by targeting the VEGF/VEGFR2/AKT signaling pathway. Experimental and Therapeutic Medicine, 23, 360. https://doi.org/10.3892/etm.2022.11287
MLA
Li, X., Li, Y., Wang, Y., Liu, F., Liu, Y., Liang, J., Zhan, R., Wu, Y., Ren, H., Zhang, X., Liu, J."Sinensetin suppresses angiogenesis in liver cancer by targeting the VEGF/VEGFR2/AKT signaling pathway". Experimental and Therapeutic Medicine 23.5 (2022): 360.
Chicago
Li, X., Li, Y., Wang, Y., Liu, F., Liu, Y., Liang, J., Zhan, R., Wu, Y., Ren, H., Zhang, X., Liu, J."Sinensetin suppresses angiogenesis in liver cancer by targeting the VEGF/VEGFR2/AKT signaling pathway". Experimental and Therapeutic Medicine 23, no. 5 (2022): 360. https://doi.org/10.3892/etm.2022.11287
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