| Literature DB >> 33743348 |
Young-Seok Lee1, Suyun Jeong1, Ki-Yoon Kim2, Ji-Su Yoon1, Sungsoo Kim3, Kyung-Sik Yoon3, Joohun Ha3, Insug Kang3, Wonchae Choe4.
Abstract
Hepatocellular carcinoma (HCC) is the fifth common types of cancer with poor prognosis in the world. Honokiol (HNK), a natural biphenyl compound derived from the magnolia plant, has been reported to exert anticancer effects, but its mechanism has not been elucidated exactly. In the present study, HNK treatment significantly suppressed the migration ability of HepG2 and Hep3B human hepatocellular carcinoma. The treatment reduced the expression levels of the genes associated with cell migration, such as S100A4, MMP-2, MMP-9 and Vimentin. Interestingly, treatment with HNK significantly reduced the expression level of Cyclophilin B (CypB) which stimulates cancer cell migration. However, overexpressed CypB abolished HNK-mediated suppression of cell migration, and reversed the apoptotic effects of HNK. Altogether, we concluded that the suppression of migration activities by HNK was through down-regulated CypB in HCC. These finding suggest that HNK may be a promising candidate for HCC treatment via regulation of CypB.Entities:
Keywords: Cell viability; Cyclophilin B; Honokiol; Migration
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Year: 2021 PMID: 33743348 DOI: 10.1016/j.bbrc.2021.03.011
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575