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HLJ1 靶向药物筛选发现,穿心莲内酯这种中草药可以抑制非小细胞肺癌的肿瘤生长和侵袭。

The HLJ1-targeting drug screening identified Chinese herb andrographolide that can suppress tumour growth and invasion in non-small-cell lung cancer.

机构信息

Institute of Molecular Biology, National Chung Hsing University, Taichung, Taiwan, Republic of China.

出版信息

Carcinogenesis. 2013 May;34(5):1069-80. doi: 10.1093/carcin/bgt005. Epub 2013 Jan 9.

Abstract

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.

摘要

HLJ1 是一种新型肿瘤抑制因子,是治疗非小细胞肺癌(NSCLC)的潜在药物靶点。在本报告中,我们使用含有启动子的增强子区域作为 HLJ1 靶向药物筛选平台,从中药库中鉴定出几种具有增强 HLJ1 启动子活性、抑制 NSCLC 肿瘤生长和侵袭能力的中草药。在所鉴定的中草药中,穿心莲内酯(来自穿心莲)最显著地诱导 HLJ1 表达,并在体外和体内均抑制肿瘤发生。穿心莲内酯通过 JunB 激活上调 HLJ1,从而调节 MMP-2 启动子处的 AP-2α 结合并抑制 MMP-2 的表达。此外,HLJ1 的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。我们表明,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、凋亡和粘附相关的生物学信号转导,包括丝裂原活化蛋白激酶、粘着斑和紧密连接途径,表明穿心莲内酯对抗癌侵袭和增殖具有多种作用。总之,HLJ1 靶向药物筛选平台可用于筛选新型抗癌化合物。使用该平台,我们鉴定出穿心莲内酯是一种有前途的新型抗癌药物,可抑制 NSCLC 中的肿瘤生长和侵袭。

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