PI3K/AKT/mTOR通路
山奈酚
蛋白激酶B
细胞凋亡
体内
结直肠癌
细胞生长
化学
药理学
生物化学
癌症
癌症研究
生物
医学
槲皮素
内科学
生物技术
抗氧化剂
作者
Yufei Zhai,Jing Sun,Chengtao Sun,Huan Zhao,Xuan Li,Jiaxiong Yao,Jiajia Su,Xiaoqian Xu,Xiukun Xu,Jiang‐Ning Hu,Maria Daglia,Bing Han,Guoyin Kai
摘要
Abstract The dried root of Tetrastigma hemsleyanum Diels et Gilg is used as a traditional Chinese medicine in southern China, as a folk remedy for carcinomas and gastrointestinal diseases. The total flavonoids of T. hemsleyanum (THTF) provide its main bioactive constituents. However, the mechanisms underlying its potential activity on colorectal cancer are still unknown. Here, we investigated the antitumor effect of THTF on colorectal cancer in vitro and in vivo. It was found that THTF inhibited HCT‐116 and HT‐29 cell growth, with an IC 50 of 105.60 and 140.80 μg/mL, respectively. THTF suppressed clonogenicity and promoted apoptosis in HCT‐116. In vivo, THTF (120 mg/kg) delayed tumor growth in HCT‐116 xenografts without influencing on body weight, organ pathology and indexes, and blood routine level. Mechanistically, THTF inhibited the expression of PI3K, AKT, and mTOR at the protein level and transcriptional levels. Molecular docking indicated eight compounds in THTF (kaempferol 3‐rutinoside, rutinum, isoquercitrin, L‐epicatechin, quercetin, astragalin, kaempferol 3‐sambubioside, and catechin) strongly bound with amino acid sites of PI3K and mTOR proteins, indicating a high affinity. The results suggest that THTF delayed colorectal tumor growth by inhibiting the PI3K/AKT/mTOR pathway and might be a potential candidate for colorectal cancer prevention.
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