木樨草素通过靶向miR-6809-5p/FLOT1/FAK并引发肝细胞癌中的EMT来抑制细胞迁移和侵袭

IF 5 2区 医学 Q2 Medicine
Pei-Wei Yang , Su-Ping Ma , Xin-Ju Chen , Fang-Ming Yang , Shou-Mei Wang , Qian Wang , Shu-Hui Zhang
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引用次数: 0

摘要

木犀草素,3′,4′,5,7-四羟基黄酮,是一种天然的类黄酮成分,存在于各种中草药中,如黄芩、金银花、菊花、荆芥和卧卧草,具有预防和治疗癌症的潜力。本研究在体外和体内研究了黄芩有效成分木犀草素抑制肝癌细胞侵袭转移的分子机制。在HCC细胞中发现致癌microRNA miR-6809-5p异常上调,木犀草素下调;过表达miR-6809-5p能够通过miR-6809-5p /FLOT1/FAK信号通路恢复木樨素的抗hcc作用。此外,木贼素通过调节PI3K/AKT/mTOR通路抑制HCC侵袭、转移和上皮间质转化(EMT),影响E-cadherin、β-catenin、Vimentin、N-cadherin、Snail、Twist和Slug等标志物。本研究表明木犀草素在体外和体内均能有效抑制HCC细胞的迁移和侵袭,显著抑制上皮间充质转化(epithelial mesenchymal transition, EMT)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Luteolin suppresses cell migration and invasion via targeting miR-6809-5p/FLOT1/FAK and eliciting EMT in hepatocellular carcinoma
Luteolin, 3′,4′,5,7-tetrahydroxyflavone, a natural flavonoid component found in various Chinese herbs such as Scutellaria barbata D. Don, honeysuckle, chrysanthemum, schizonepeta, and ajuga decumbens, exhibits potential for cancer prevention and therapy. This study elucidates the molecular mechanisms by which luteolin, an active constituent of Scutellaria barbata, inhibits invasion and metastasis of hepatocellular carcinoma (HCC) cell lines both in vitro and in vivo. The oncogenic microRNA miR-6809–5p was found to be aberrantly upregulated in HCC tissues and downregulated by luteolin in HCC cells; overexpression of miR-6809–5p was able to restore the anti-HCC effects of luteolin via the miR-6809–5p/FLOT1/FAK signaling pathway. Furthermore, luteolin suppressed HCC invasion, metastasis, and epithelial-mesenchymal transition (EMT) through modulation of the PI3K/AKT/mTOR pathway, affecting markers such as E-cadherin, β-catenin, Vimentin, N-cadherin, Snail, Twist, and Slug. This research demonstrates that luteolin effectively inhibits HCC cell migration and invasion and significantly suppresses epithelial mesenchymal transition (EMT) both in vitro and in vivo.
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来源期刊
CiteScore
8.40
自引率
2.00%
发文量
314
审稿时长
54 days
期刊介绍: Translational Oncology publishes the results of novel research investigations which bridge the laboratory and clinical settings including risk assessment, cellular and molecular characterization, prevention, detection, diagnosis and treatment of human cancers with the overall goal of improving the clinical care of oncology patients. Translational Oncology will publish laboratory studies of novel therapeutic interventions as well as clinical trials which evaluate new treatment paradigms for cancer. Peer reviewed manuscript types include Original Reports, Reviews and Editorials.
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