Proanthocyanidins extracted from grape seeds inhibit the growth of hepatocellular carcinoma cells and induce apoptosis through the MAPK/AKT pathway
文献类型: 外文期刊
作者: Zheng, Wancai 1 ; Feng, Yujing 4 ; Bai, Yujia 2 ; Feng, Zuoshan 2 ; Yang, Xijuan 1 ; Dang, Bin 1 ; Xiao, Ming 1 ; Zhang, Jianmei 2 ; Han, Sheng-Qiang 2 ;
作者机构: 1.Qinghai Univ, Qinghai Acad Agr & Forestry Sci, Xining 810016, Peoples R China
2.Xinjiang Agr Univ, Coll Food Sci & Pharmacol, Urumqi 830052, Peoples R China
3.Xinjiang Agr Univ, Xinjiang Key Lab Postharvest Sci & Technol Fruits, Urumqi 830052, Peoples R China
4.Shanghai Punan Hosp Pudong New Dist, Shanghai 200120, Peoples R China
关键词: Grape seed proanthocyanidins; Hepatocellular carcinoma; Proliferation; Apoptosis
期刊名称:FOOD BIOSCIENCE ( 影响因子:5.318; 五年影响因子:5.846 )
ISSN: 2212-4292
年卷期: 2022 年 45 卷
页码:
收录情况: SCI
摘要: Proanthocyanidins naturally occur in various fruits, some vegetables and beverages. Increasing evidence has shown that dietary intake of proanthocyanidins is a promising alternative to tumor chemoprevention or chemotherapy. Grape seeds are the most abundant source of proanthocyanidins, and grape seed proanthocyanidins (GSPs) show an anticancer effect on hepatocellular carcinoma (HCC), which accounts for approximately 85-90% of all primary liver malignancies. Although an increasing number of studies have investigated the effects of GSPs on HCC and the associated mechanisms, the precise mechanism of GSP therapy in HCC remains unclear. This study aimed to understand the cytotoxic effect of GSPs on HepG2 cells by investigating morphology and growth inhibition. Cell proliferation and apoptosis were estimated by an MTT assay and flow cytometry, and the protein expression of HepG2 cells was determined through Western blotting. The results indicated that GSPs could markedly inhibit HepG(2) liver cancer cells and induce apoptosis, with the effects varying by dose and treatment time. Furthermore, GSPs inhibited the phosphorylation of extracellular regulated protein kinases (ERK), c-Jun NH2-terminal kinase (JNK), p38 mitogen-activated protein kinase (p38 MAPK), I Kappa B alpha, pyruvate dehydrogenase kinase 1 (PDK1), glycogen synthase kinase-3 beta (GSK3 beta) and protein kinase B (AKT), which accounted for the inactivation of mitogen-activated protein kinase/AKT (MAPK/AKT) pathways. These results indicate that GSPs are a potential source of natural chemopreventive agents for the treatment of HCC.
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