Catechol inhibits epidermal growth factor-induced epithelial-to-mesenchymal transition and stem cell-like properties in hepatocellular carcinoma cells

被引:17
|
作者
Lim, Won-Chul [1 ]
Kim, Hyunhee [2 ]
Kim, Young-Joo [3 ]
Jeon, Bu-Nam [4 ]
Kang, Hee-Bum [5 ]
Ko, Hyeonseok [6 ]
机构
[1] Korea Food Res Inst, Jeonju Si, Jeollabuk Do, South Korea
[2] Univ Ulsan, Coll Med, AMIST, Asan Med Ctr,Dept Biomed Sci, Seoul, South Korea
[3] Korea Inst Sci & Technol, Nat Prod Res Ctr, Kangnung, Gangwon Do, South Korea
[4] Genome & Co, Pangyo Ro 253, Seongnam Si, Gyeonggi Do, South Korea
[5] Voronol Res Inst, IT Ctr, S 12th F,Songdogwahak Ro 32, Incheon, South Korea
[6] HLB Life Sci, Teheran Ro 420, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
MATRIX METALLOPROTEINASE-2; MOLECULAR-MECHANISMS; CANCER; ACTIVATION; INVASION; EGFR; PROLIFERATION; PLASTICITY; PATHWAYS; TISSUE;
D O I
10.1038/s41598-020-64603-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Epithelial-mesenchymal transition (EMT) is a major cellular process in which epithelial cells lose cell polarity and cell-cell adhesion and become motility and invasiveness by transforming into mesenchymal cells. Catechol is one of the natural compounds present in fruits and vegetables and has various pharmacological and physiological activities including anti-carcinogenic effects. However, the effects of catechol on EMT has not been reported. Epidermal growth factor (EGF) is one of the growth factors and is known to play a role in inducing EMT. The present study showed that catechol suppressed not only the morphological changes to the mesenchymal phenotype of epithelial HCC cells, but also the reduction of E-cadherin and the increment of Vimentin, which are typical hallmark of EMT. In addition, catechol suppressed EMT-related steps such as migration, invasion, anoikis resistance acquisition, and stem cell-like characterization through the EGFR-AKT-ERK signaling pathway during liver cancer metastasis. Therefore, these results suggest that catechol may be able to regulate the early metastasis of liver cancer in vitro.
引用
收藏
页数:14
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