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Anti-cancer effects of baicalein in non-small cell lung cancer in-vitro and in-vivo

机译:黄ical素对非小细胞肺癌的体内外抗癌作用

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Background Baicalein is a widely used Chinese herbal medicine derived from Scutellaria baicalenesis , which has been traditionally used as anti-inflammatory and anti-cancer therapy. In this study we examined the anti-tumour pathways activated following baicalein treatment in non-small cell lung cancer (NSCLC), both in-vitro and in-vivo. Methods The effect of baicalein treatment on H-460 cells in-vitro was assessed using both BrdU assay (cell proliferation) and High Content Screening (multi-parameter apoptosis assay). A xenograft nude mouse model was subsequently established using these cells and the effect of baicalein on tumour growth and survival assessed in-vivo. Tumours were harvested from these mice and histological tissue analysis carried out. VEGF, 12-lipoxygenase and microvessel density (CD-31) were assessed by immunohistochemistry (IHC), while H and E staining was carried out to assess mitotic index. Gene expression profiling was carried out on corresponding RNA samples using Human Cancer Pathway Finder Arrays and qRT-PCR, with further gene expression analysis carried out using qRT-PCR. Results Baicalein significantly decreased lung cancer proliferation in H-460 cells in a dose dependent manner. At the functional level, a dose-dependent induction in apoptosis associated with decreased cellular f -actin content, an increase in nuclear condensation and an increase in mitochondrial mass potential was observed. Orthotopic treatment of experimental H-460 tumours in athymic nude mice with baicalein significantly ( p Conclusion This study is the first to demonstrate efficacy of baicalein both in-vitro and in-vivo in NSCLC. These effects may be mediated in part through a reduction in both cell cycle progression and angiogenesis. At the molecular level, alterations in expression of VEGF , FGFR-2 , and RB-1 have been implicated, suggesting a molecular mechanism underlying this in-vivo effect.
机译:背景技术黄ical素是从黄cut中提取的一种广泛使用的中草药,传统上一直用作抗炎和抗癌疗法。在这项研究中,我们研究了黄ical苷治疗后在体外和体内的非小细胞肺癌(NSCLC)中激活的抗肿瘤途径。方法采用BrdU分析(细胞增殖)和高内涵筛选(多参数凋亡分析)评估黄ical苷对H-460细胞的体外作用。随后使用这些细胞建立异种移植裸鼠模型,并在体内评估黄ical素对肿瘤生长和存活的影响。从这些小鼠中收获肿瘤,并进行组织学分析。通过免疫组织化学(IHC)评估VEGF,12-脂氧合酶和微血管密度(CD-31),同时进行H和E染色以评估有丝分裂指数。使用Human Cancer Pathway Finder Arrays和qRT-PCR对相应的RNA样品进行基因表达谱分析,并使用qRT-PCR进行进一步的基因表达分析。结果黄ical苷以剂量依赖性方式显着降低了H-460细胞中的肺癌增殖。在功能水平上,观察到凋亡的剂量依赖性诱导,其与细胞内β-肌动蛋白含量降低,核浓缩增加和线粒体质量潜能增加有关。黄e苷显着原位治疗无胸腺裸鼠的实验性H-460肿瘤(p结论该研究首次证明了黄e苷在NSCLC中的体内和体外疗效。在分子水平上,涉及到VEGF,FGFR-2和RB-1表达的改变,暗示了这种体内作用的分子机制。

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