Total flavonoids from the dried root of Tetrastigma hemsleyanum Diels et Gilg inhibit colorectal cancer growth through PI3K/AKT/mTOR signaling pathway.
Yufei ZhaiJing SunChengtao SunHuan ZhaoXuan LiJiaxiong YaoJiajia SuXiaoqian XuXiukun XuJiangning HuMaria DagliaBing HanGuoyin KaiPublished in: Phytotherapy research : PTR (2022)
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.
Keyphrases
- cell cycle arrest
- pi k akt
- signaling pathway
- molecular docking
- cell proliferation
- body weight
- cell death
- amino acid
- epithelial mesenchymal transition
- poor prognosis
- induced apoptosis
- gene expression
- molecular dynamics simulations
- endoplasmic reticulum stress
- clinical practice
- mass spectrometry
- climate change
- single molecule
- heat shock protein