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Diospyros kaki leaves inhibit HGF/Met signaling-mediated EMT and stemness features in hepatocellular carcinoma

Authors
 Hyeonseok Ko  ;  Gyuwon Huh  ;  Sang Hoon Jung  ;  Hyukjoon Kwon  ;  Youngsic Jeon  ;  Young Nyun Park  ;  Young-Joo Kim 
Citation
 FOOD AND CHEMICAL TOXICOLOGY, Vol.142 : 111475, 2020-08 
Journal Title
FOOD AND CHEMICAL TOXICOLOGY
ISSN
 0278-6915 
Issue Date
2020-08
MeSH
Carcinoma, Hepatocellular / metabolism ; Carcinoma, Hepatocellular / pathology* ; Cell Line, Tumor ; Diospyros / chemistry* ; Epithelial-Mesenchymal Transition / drug effects* ; Hepatocyte Growth Factor / metabolism* ; Humans ; Liver Neoplasms / metabolism ; Liver Neoplasms / pathology* ; Neoplastic Stem Cells / drug effects* ; Plant Extracts / pharmacology* ; Plant Leaves / chemistry* ; Proto-Oncogene Proteins c-met / metabolism* ; Signal Transduction / drug effects*
Keywords
Diospyros kaki leaves ; EMT ; HGF/Met signaling ; Hepatocellular carcinoma ; Stemness
Abstract
Persimmon (Diospyros kaki L.f.) trees are widely cultivated for their edible fruits in Asia. D. kaki leaves are abundant in phytochemicals that have numerous medicinal properties. Hepatocyte growth factor (HGF) and its receptor Met lead to poor prognosis via the promotion of metastasis and chemoresistance in hepatocellular carcinoma (HCC). Therefore, inhibitors targeting the HGF/Met pathway are regarded as promising drugs against HCC. Here, we investigated the effects of D. kaki leaves on HGF-induced epithelial-to-mesenchymal transition (EMT) and stemness traits in HCC. The ethanol extract of D. kaki leaves (EEDK) markedly suppressed HGF-mediated cell migration and invasion through upregulation of CDH1 and downregulation of SNAI1, VIM, MMP1, MMP2, and MMP9. Moreover, EEDK increased the cytotoxicity of sorafenib, which was reduced by HGF, and decreased the expression of the stemness markers KRT19 and CD44. Additionally, we found a clear correlation between stemness and EMT markers in HCC patients. Importantly, EEDK reduced Met activity and attenuated HGF-mediated activation of JNK/c-Jun. Our findings provide new evidence that EEDK can ameliorate HCC with poor prognosis and aggressive phenotype by blocking HGF/Met signaling.
Full Text
https://www.sciencedirect.com/science/article/pii/S0278691520303653
DOI
10.1016/j.fct.2020.111475
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
Yonsei Authors
Park, Young Nyun(박영년) ORCID logo https://orcid.org/0000-0003-0357-7967
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/182613
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