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首页> 外文期刊>Carcinogenesis >The HLJ1-targeting drug screening identified Chinese herb andrographolide that can: Suppress tumour growth and invasion in non-small-cell lung cancer
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The HLJ1-targeting drug screening identified Chinese herb andrographolide that can: Suppress tumour growth and invasion in non-small-cell lung cancer

机译:靶向HLJ1的药物筛选确定了中药穿心莲内酯可以:抑制非小细胞肺癌的肿瘤生长和侵袭

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摘要

HLJ1 is a novel tumour suppressor and is a potential druggable target for non-small-cell lung cancer (NSCLC). In this report, using a promoter-containing enhancer region as the HLJ1-targeting drug-screening platform, we identified several herbal compounds from a Chinese herbal bank with the capacity to enhance HLJ1 promoter activity and suppress tumour growth and invasion of NSCLC. Among the herbal drugs identified, the andrographolide (from Andrographis paniculata [Burm. f.] Nees.) most significantly induced HLJ1 expression and suppressed tumorigenesis both in vitro and in vivo. The andrographolide upregulates HLJ1 via JunB activation, which modulates AP-2α binding at the MMP-2 promoter and represses the expression of MMP-2. In addition, silencing of HLJ1 partially reverses the inhibition of cancer-cell invasion by andrographolide. Microarray transcriptomic analysis was performed to comprehensively depict the andrographolide-regulated signalling pathways. We showed that andrographolide can affect 939 genes (analysis of variance, false discovery rate < 0.05) that are dominantly involved in the cell cycle, apoptosis and adhesion-related biological signalling, including mitogen-activated protein kinase, focal adhesion and tight junction pathways, indicating the diverse effects of andrographolide on anticancer invasion and proliferation. In conclusion, the HLJ1-targeting drug-screening platform is useful for screening of novel anticancer compounds. Using this platform, we identified andrographolide is a promising new anticancer agent that could suppress tumour growth and invasion in NSCLC.
机译:HLJ1是一种新型的肿瘤抑制剂,是非小细胞肺癌(NSCLC)的潜在可药物治疗靶标。在本报告中,我们使用含有启动子的增强子区域作为靶向HLJ1的药物筛选平台,我们从中草药库中鉴定了几种具有增强HLJ1启动子活性并抑制肿瘤生长和NSCLC侵袭能力的草药化合物。在鉴定出的草药中,穿心莲内酯(来自穿心莲[Burm。f。] Nees。)在体外和体内均能最明显地诱导HLJ1表达并抑制肿瘤发生。穿心莲内酯通过JunB激活上调HLJ1,JunB激活可调节MMP-2启动子处的AP-2α结合并抑制MMP-2的表达。此外,HLJ1沉默部分逆转了穿心莲内酯对癌细胞侵袭的抑制作用。进行了微阵列转录组分析以全面描述穿心莲内酯调节的信号通路。我们发现穿心莲内酯可以影响939个基因(方差分析,错误发现率<0.05),这些基因主要参与细胞周期,细胞凋亡和与粘附有关的生物信号传导,包括促分裂原激活的蛋白激酶,黏着斑粘附和紧密连接途径,表明穿心莲内酯对抗癌侵袭和增殖的不同作用。总之,靶向HLJ1的药物筛选平台可用于筛选新型抗癌化合物。使用该平台,我们确定穿心莲内酯是一种有前途的新型抗癌剂,可以抑制NSCLC中的肿瘤生长和侵袭。

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