首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Basil polysaccharide attenuates hepatocellular carcinoma metastasis in rat by suppressing H3K9me2 histone methylation under hepatic artery ligation-induced hypoxia
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Basil polysaccharide attenuates hepatocellular carcinoma metastasis in rat by suppressing H3K9me2 histone methylation under hepatic artery ligation-induced hypoxia

机译:通过抑制肝动脉结扎诱导的缺氧,罗勒多糖通过抑制H3K9ME2组蛋白甲基化抑制大鼠的肝细胞癌转移

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摘要

Hepatocellular carcinoma (HCC) is one of the most common and fatal cancers in the world. Tumor metastasis is an important factor of poor prognosis in patients with HCC. Tumor hypoxia can promote tumor cell metastasis in HCC. Epigenetic modification is closely related to tumor hypoxia and metastasis. In our previous research, we found that basil polysaccharide suppressed migration and invasion of HCC cell by inhibiting hypoxia induced histone methylation in vitro. In the present study, we investigated the effect of basil polysaccharide on the walker 256 carcinoma cell metastasis in rat. We established an intratumoral hypoxic model in rat by hepatic artery ligation (HAL). Then rats were treated with basil polysaccharide (75, 150 and 300 mg/kg). The results showed that HAL could promote tumor metastasis by aggravating tumor hypoxia. However, basil polysaccharide could inhibit tumor metastasis in intratumoral hypoxia. Further, we demonstrated that basil polysaccharide could down-regulate the expression of HIF-1 alpha, G9a, LSD1, JMJD1A, JMJD2B, JARID1 B and H3K9me2. Synchronously, basil polysaccharide could increase E-cadherin and VMP1 expression, and decrease N-cadherin, vimentin and beta-catenin expression. The results indicated that histone modifying enzymes might be a new therapeutic target of basil polysaccharide on hepatocellular carcinoma metastasis. (C) 2017 Elsevier B.V. All rights reserved.
机译:肝细胞癌(HCC)是世界上最常见和最常见的癌症之一。肿瘤转移是HCC患者预后不良的重要因素。肿瘤缺氧可以促进HCC中的肿瘤细胞转移。表观遗传修饰与肿瘤缺氧和转移密切相关。在我们以前的研究中,我们发现通过抑制体外缺氧诱导的组蛋白甲基化抑制罗勒多糖抑制了HCC细胞的迁移和侵袭。在本研究中,我们研究了罗勒多糖对大鼠步行者256癌细胞转移的影响。我们通过肝动脉连接(HAL)在大鼠中建立了肿瘤内缺氧模型。然后用罗勒多糖(75,150和300mg / kg)处理大鼠。结果表明,通过加剧肿瘤缺氧来促进肿瘤转移。然而,罗勒多糖可以抑制肿瘤缺氧中的肿瘤转移。此外,我们证明罗勒多糖可以下调HIF-1α,G9A,LSD1,JMJD1A,JMJD2B,JARID1B和H3K9ME2的表达。同步,罗勒多糖可以增加E-Cadherin和VMP1表达,并降低N-Cadherin,Vimentin和β-连环蛋白的表达。结果表明,组蛋白改性酶可能是猪多糖对肝细胞癌转移的新治疗靶标。 (c)2017年Elsevier B.V.保留所有权利。

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