Baicalein suppresses the proliferation and invasiveness of colorectal cancer cells by inhibiting Snail-induced epithelial-mesenchymal transition

被引:23
|
作者
Zeng, Qiongyao [1 ,2 ]
Zhang, Yu [3 ,4 ]
Zhang, Wenjing [2 ,5 ]
Guo, Qiang [1 ,2 ,3 ]
机构
[1] Kunming Univ Sci & Technol, Fac Life Sci & Biotechnol, Kunming 650500, Yunnan, Peoples R China
[2] Kunming Univ Sci & Technol, Fac Med, 727 South Jingming Rd, Kunming 650500, Yunnan, Peoples R China
[3] First Peoples Hosp Yunnan Prov, Dept Gastroenterol, 157 Jinbi Rd, Kunming 650032, Yunnan, Peoples R China
[4] First Peoples Hosp Yunnan Prov, Yunnan Prov Inst Digest Med, Kunming 650032, Yunnan, Peoples R China
[5] First Peoples Hosp Yunnan Prov, Dept Med Oncol, Kunming 650032, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
colorectal cancer; baicalein; Snail; epithelial-mesenchymal transition; p53; p21; TRADITIONAL CHINESE MEDICINE; FLAVONOIDS; APOPTOSIS; EMT; MIGRATION; EXTRACTS; INVASION;
D O I
10.3892/mmr.2020.11051
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Scutellaria baicalensis (S. baicalensis) is a plant that is widely used for medicinal purposes. Baicalein, one of the primary bioactive compounds found in S. baicalensis, is thought to possess antitumor activity, although the specific mechanisms remain unclear. Therefore, the present study aimed to evaluate the ability of baicalein to disrupt the proliferation and metastatic potential of colorectal cancer (CRC) cells; a rapid and sensitive ultra-high performance liquid chromatography-tandem mass spectrometric method was employed for the identification of baicalein in an S. baicalensis aqueous extract and in rat plasma. To investigate the effects of baicalein, Cell Counting Kit-8 (CCK-8), western blotting, wound-healing and Transwell assays were performed. The data indicated that baicalein was absorbed into the blood and was able to effectively disrupt the proliferation, migration and invasion abilities of CRC cells in a dose- and time-dependent manner. Baicalein treatment was also revealed to decrease the expression of epithelial-mesenchymal transition (EMT)-promoting factors including vimentin, Twist1, and Snail, but to upregulate the expression of E-cadherin in CRC cells. The expression levels of cell cycle inhibitory proteins p53 and p21 also increased following baicalein treatment. In addition, Snail-induced vimentin and Twist1 upregulation, as well as E-cadherin downregulation, were reversed following treatment with baicalein. In conclusion, the results of the present study indicate that baicalein may suppress EMT, at least in part, by decreasing Snail activity.
引用
收藏
页码:2544 / 2552
页数:9
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