Procyanidin B2 induces apoptosis and autophagy in gastric cancer cells by inhibiting Akt/mTOR signaling pathway

• Published in: BMC complementary and alternative medicine 2021-02, Vol.21 (1), p.76-76, Article 76
• Main Authors: Li, Yuqin, Lu, Xiaolan, Tian, Peiying, Wang, Kai, Shi, Jianping
• Format: Article
• Language: English
• Subjects: Akt; AKT protein; Analysis; Antibodies; Anticancer properties; antineoplastic activity; Antitumor activity; Apoptosis; Autophagy; Biological effects; Cancer; Cancer cells; Cancer therapies; Care and treatment; Caspase-3; Cell culture; Cell growth; Cell proliferation; Cell viability; Cholecystokinin; complement; culture media; drugs; Gastric cancer; grape seeds; Herbal medicine; humans; L-Lactate dehydrogenase; Lactate dehydrogenase; Lactic acid; Medicinal plants; Medicine, Botanic; Medicine, Herbal; Metastasis; mTOR; Phagocytosis; Procyanidin B2; Procyanidins; protein synthesis; Proteins; Signal transduction; Signaling; Staining; Stomach cancer; stomach neoplasms; therapeutics; TOR protein; Western blotting
• ISSN: 2662-7671; 2662-7671; 1472-6882
• DOI: 10.1186/s12906-021-03225-1

Procyanidin B2 (PB2), a unique component of the grape seed and other medicinal plants. PB2 has shown wide anticancer activity in various human cancer cells. However, it remains unclear about the biological effects and associated mechanisms of PB2 on gastric cancer cells. Cell proliferation was measured by CCK8 assay, and cellular lactate dehydrogenase (LDH) release was measured in the culture medium. Cellular apoptosis was observed via TUNEL staining assay and measured by caspase-3 and -9 activities. Autophagy was observed by LC3 staining. Western blot analysis was performed to verify autophagy-associated proteins (Beclin1 and Atg5) and Akt-mTOR pathway. PB2 reduced the viability of BGC-823 and SGC-7901 cells in a concentration-dependent manner. Furthermore, PB2 induced increased apoptosis rate of gastric cancer cells and enhanced caspase-3 and -9 activities. Simultaneously, PB2 triggered autophagy in gastric cancer cells, with enhanced LC3 staining and increased expression of Beclin1 and Atg5, while the inhibition of autophagy by 3-MA reversed the PB2-induced suppression on cell viability. In addition, PB2 significantly decreased p-Akt and p-mTOR protein expression of gastric cancer cells. PB2 exerts anti-proliferative and apoptotic effects and induces autophagy by modulating Akt/mTOR signaling pathway. PB2 may be developed as a potential therapeutic drug for gastric cancer.