2-Methoxy-1,4-naphthoquinone (MNQ) regulates cancer key genes of MAPK, PI3K, and NF-κB pathways in Raji cells

Teck Yew Wong, S. Menaga, Chi-Ying F. Huang, S. H. Ho, S. Gan, Y. Lim
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引用次数: 1

Abstract

2-Methoxy-1,4-naphthoquinone (MNQ) has been shown to cause cytotoxic towards various cancer cell lines. This study is designed to investigate the regulatory effect of MNQ on the key cancer genes in mitogen-activated protein kinase, phosphoinositide 3-kinase, and nuclear factor кB signaling pathways. The expression levels of the genes were compared at different time point using polymerase chain reaction arrays and Ingenuity Pathway Analysis was performed to identify gene networks that are most significant to key cancer genes. A total of 43 differentially expressed genes were identified with 21 up-regulated and 22 down-regulated genes. Up-regulated genes were involved in apoptosis, cell cycle and act as tumor suppressor while down-regulated genes were involved in anti-apoptosis, angiogenesis, cell cycle and act as transcription factor as well as proto-oncogenes. MNQ exhibited multiple regulatory effects on the cancer key genes that targeting at cell proliferation, cell differentiation, cell transformation, apoptosis, reduce inflammatory responses, inhibits angiogenesis and metastasis.
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2-甲氧基-1,4-萘醌(MNQ)调控Raji细胞中MAPK、PI3K、NF-κB通路的肿瘤关键基因
2-甲氧基-1,4-萘醌(MNQ)对多种癌症细胞系具有细胞毒性。本研究旨在研究MNQ对癌症关键基因有丝分裂原激活蛋白激酶、磷酸肌醇3-激酶和核因子κB信号通路的调节作用。使用聚合酶链式反应阵列比较不同时间点的基因表达水平,并进行Ingenuity Pathway Analysis以确定对关键癌症基因最重要的基因网络。共鉴定出43个差异表达基因,其中21个上调,22个下调。上调的基因参与细胞凋亡、细胞周期并作为肿瘤抑制因子,而下调的基因参与抗细胞凋亡、血管生成、细胞周期,并作为转录因子和原癌基因。MNQ对癌症关键基因具有多种调节作用,靶向细胞增殖、细胞分化、细胞转化、凋亡,减少炎症反应,抑制血管生成和转移。
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