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Functional Characterisation of Anticancer Activity in the Aqueous Extract of Helicteres angustifolia L. Roots

机译:Helicoteres angustifolia L.根水提物中抗癌活性的功能表征

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摘要

Helicteres angustifolia L. is a shrub that forms a common ingredient of several cancer treatment recipes in traditional medicine system both in China and Laos. In order to investigate molecular mechanisms of its anticancer activity, we prepared aqueous extract of Helicteres angustifolia L. Roots (AQHAR) and performed several in vitro assays using human normal fibroblasts (TIG-3) and osteosarcoma (U2OS). We found that AQHAR caused growth arrest/apoptosis of U2OS cells in a dose-dependent manner. It showed no cytotoxicity to TIG-3 cells at doses up to 50 μg/ml. Biochemical, imaging and cell cycle analyses revealed that it induces ROS signaling and DNA damage response selectively in cancer cells. The latter showed upregulation of p53, p21 and downregulation of Cyclin B1 and phospho-Rb. Furthermore, AQHAR-induced apoptosis was mediated by increase in pro-apoptotic proteins including cleaved PARP, caspases and Bax. Anti-apoptotic protein Bcl-2 showed decrease in AQHAR-treated U2OS cells. In vivo xenograft tumor assays in nude mice revealed dose-dependent suppression of tumor growth and lung metastasis with no toxicity to the animals suggesting that AQHAR could be a potent and safe natural drug for cancer treatment.
机译:Helicteres angustifolia L.是一种灌木,是中国和老挝传统医学体系中几种癌症治疗方法的常用成分。为了研究其抗癌活性的分子机制,我们制备了Helicteres angustifolia L. Roots(AQHAR)的水提物,并使用人正常成纤维细胞(TIG-3)和骨肉瘤(U2OS)进行了几种体外测定。我们发现,AQHAR以剂量依赖性方式引起U2OS细胞的生长停滞/凋亡。剂量高达50μg/ ml时,对TIG-3细胞无细胞毒性。生化,成像和细胞周期分析表明,它在癌细胞中选择性诱导ROS信号传导和DNA损伤反应。后者显示出p53,p21的上调和细胞周期蛋白B1和磷酸Rb的下调。此外,AQHAR诱导的凋亡是由促凋亡蛋白(包括裂解的PARP,胱天蛋白酶和Bax)的增加介导的。抗凋亡蛋白Bcl-2在经AQHAR处理的U2OS细胞中显示出下降。在裸鼠体内进行的异种移植肿瘤试验显示,剂量依赖性抑制肿瘤生长和肺转移,对动物无毒性,这表明AQHAR可能是用于癌症治疗的有效且安全的天然药物。

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