OncoTargets and Therapy (Jan 2022)

Stichoposide C Exerts Anticancer Effects on Ovarian Cancer by Inducing Autophagy via Inhibiting AKT/mTOR Pathway

  • Liu F,
  • Tang L,
  • Tao M,
  • Cui C,
  • He D,
  • Li L,
  • Liao Y,
  • Gao Y,
  • He J,
  • Sun F,
  • Lin H,
  • Li H

Journal volume & issue
Vol. Volume 15
pp. 87 – 101

Abstract

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Fangfang Liu,1,* Lumin Tang,2,* Mengyu Tao,3,* Chuang Cui,1 Di He,2 Longxia Li,2 Yahui Liao,4 Yamin Gao,5 Jing He,5 Fan Sun,6 Houwen Lin,6 He Li1,2 1Shanghai University of Traditional Chinese Medicine, Shanghai, People’s Republic of China; 2Traditional Chinese Medicine Department, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, People’s Republic of China; 3Department of Gynecology and Obstetrics, Shanghai Key Laboratory of Gynecology Oncology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, People’s Republic of China; 4Shanghai Ocean University, Shanghai, People’s Republic of China; 5Shenyang Pharmaceutical University, Benxi, People’s Republic of China; 6Research Center for Marine Drugs, State Key Laboratory of Oncogenes and Related Genes, Department of Pharmacy, RenJi Hospital, School of Medicine, Shanghai JiaoTong University, Shanghai, People’s Republic of China*These authors contributed equally to this workCorrespondence: He Li; Fan Sun Tel +86 21 51322222; +86 21 68383339Email [email protected]; [email protected]: Stichoposide C (STC) is a triterpene glycoside isolated from Thelenota ananas, which is previously demonstrated to wide spectrum of anticancer effects against various tumor cells. However, the antitumor effects and underlying molecular mechanisms in ovarian cancer (OC) cells are not fully understood. Here, we examined if and through which mechanisms STC exerts anticancer effects on OC.Methods: CCK-8 and colony formation assays were used to detect cell viability and proliferation. Flow cytometry was used to detect apoptosis and cell cycle arrest. Protein expression and phosphorylation were measured by Western blotting analysis. Confocal fluorescence microscopy was used to observe the autophagy flux. Autophagosome formation was observed via transmission electron microscopy. Antitumor effect of STC was investigated in patient-derived organoids (PDOs) and A2780 subcutaneous xenograft tumors.Results: STC was found that not only exerted antiproliferation activity and apoptosis but also induced autophagy. Mechanistically, STC induced autophagy via inhibited the AKT/mTOR signaling pathway in ovarian cancer cells. In addition, STC and an autophagy inhibitor 3-methyladenine (3-MA) combination treatment showed significant synergetic effects on inhibiting proliferation and promoting apoptosis in vitro. Consistent with cell experiments, STC also inhibited the growth of two OC PDOs. Finally, STC markedly reduced the growth of A2780 subcutaneous xenograft tumors without organ toxicity and activated autophagy in vivo.Conclusion: Stichoposide C exerts in vitro and in vivo anticancer effects on ovarian cancer by inducing autophagy via inhibiting AKT/mTOR pathway. The findings warrant further prove for STC as a potential therapeutic agent for ovarian cancer.Keywords: ovarian cancer, stichoposide C, autophagy, apoptosis, AKT/mTOR

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