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首页> 外文期刊>Scientific reports. >Inotilone from Inonotus linteus suppresses lung cancer metastasis in vitro and in vivo through ROS-mediated PI3K/AKT/MAPK signaling pathways
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Inotilone from Inonotus linteus suppresses lung cancer metastasis in vitro and in vivo through ROS-mediated PI3K/AKT/MAPK signaling pathways

机译:来自Inonotus linteus的Inotilone通过ROS介导的PI3K / AKT / MAPK信号通路在体内外抑制肺癌转移

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Metastasis is one of the main causes of mortality in cancer patients. Inotilone, a major component of Inonotus linteus, is a traditional Chinese medical herb. In this study, MTT results showed that inotilone had no obvious cytotoxicity. Animal model results revealed that inotilone suppressed cancer metastatic efficacy. Serum results showed that inotilone reduced the activity of matrix metalloproteinase (MMP)-2 and -9 and tumor necrosis factor alpha (TNF-α) activity as well as NO content. Additionally, inotilone affected MMP-9 and tissue inhibitor of metalloproteinase (TIMP)-2 protein expression and improved the activity of the antioxidant enzymes in the lung tissues of LLC-bearing mice. In addition, cell experimental results showed that inotilone reduced the activity of MMP-2/-9 and inhibited the ability for cellular migration and invasion. Inotilone decreased interleukin (IL)-8 expression in A549 cells. Western blot results revealed that inotilone affected the protein expression of MMPs, nitric oxide synthase (iNOS), cyclooxygenase (COX)-2, anti-oxidant enzymes, mitogen activated protein kinase (MAPK), focal adhesion kinase (FAK), phosphoinositide-3 kinase (PI3K)-AKT, and nuclear factor (NF)κB. Therefore, we propose that inotilone is a potential therapeutic candidate against metastatic lung cancer cells.
机译:转移是癌症患者死亡的主要原因之一。 Inotinotus linteus的主要成分Inotilone是中药。在这项研究中,MTT结果表明,inotilone没有明显的细胞毒性。动物模型结果显示,因替洛酮可抑制癌症的转移功效。血清结果显示,因替洛酮可降低基质金属蛋白酶(MMP)-2和-9的活性以及肿瘤坏死因子α(TNF-α)的活性以及NO含量。此外,inotilone影响MMP-9和金属蛋白酶组织抑制剂(TIMP)-2的蛋白表达,并改善了LLC小鼠肺组织中抗氧化酶的活性。此外,细胞实验结果表明,因替洛酮降低了MMP-2 / -9的活性,并抑制了细胞迁移和侵袭的能力。因替洛尼降低了A549细胞中的白介素(IL)-8表达。 Western印迹结果表明,因替洛酮影响MMP,一氧化氮合酶(iNOS),环氧合酶(COX)-2,抗氧化酶,促分裂原活化蛋白激酶(MAPK),粘着斑激酶(FAK),磷酸肌醇3的蛋白表达激酶(PI3K)-AKT和核因子(NF)κB。因此,我们提出,inotilone是针对转移性肺癌细胞的潜在治疗候选药物。

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