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厚朴酚通过下调亲环素B的表达来抑制肝癌细胞迁移。

Honokiol inhibits hepatoma carcinoma cell migration through downregulated Cyclophilin B expression.

作者信息

Lee Young-Seok, Jeong Suyun, Kim Ki-Yoon, Yoon Ji-Su, Kim Sungsoo, Yoon Kyung-Sik, Ha Joohun, Kang Insug, Choe Wonchae

机构信息

Department of Biomedical Science, Graduate School, Kyung Hee University, Seoul, 02447, Republic of Korea.

Department of Biochemistry and Molecular Biology, School of Medicine, Kyung Hee University, Seoul, 02447, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2021 May 7;552:44-51. doi: 10.1016/j.bbrc.2021.03.011. Epub 2021 Mar 17.

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.

摘要

肝细胞癌(HCC)是全球第五大常见癌症,预后较差。厚朴酚(HNK)是一种从木兰植物中提取的天然联苯化合物,据报道具有抗癌作用,但其机制尚未完全阐明。在本研究中,HNK处理显著抑制了HepG2和Hep3B人肝癌细胞的迁移能力。该处理降低了与细胞迁移相关基因的表达水平,如S100A4、MMP-2、MMP-9和波形蛋白。有趣的是,HNK处理显著降低了刺激癌细胞迁移的亲环素B(CypB)的表达水平。然而,过表达的CypB消除了HNK介导的细胞迁移抑制,并逆转了HNK的凋亡作用。总之,我们得出结论,HNK对迁移活性的抑制是通过下调肝癌细胞中的CypB实现的。这些发现表明,HNK可能是通过调节CypB治疗肝癌的一个有前景的候选药物。

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