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Effects of Crude Extracts from Medicinal Herbs Rhazya stricta and Zingiber officinale on Growth and Proliferation of Human Brain Cancer Cell Line In Vitro

机译:药材生根和生姜的粗提物对人脑癌细胞株体外生长和增殖的影响

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摘要

Hitherto, limited clinical impact has been achieved in the treatment of glioblastoma (GBMs). Although phytochemicals found in medicinal herbs can provide mankind with new therapeutic remedies, single agent intervention has failed to bring the expected outcome in clinical trials. Therefore, combinations of several agents at once are gaining increasing attractiveness. In the present study, we investigated the effects of crude alkaloid (CAERS) and flavonoid (CFEZO) extracts prepared from medicinal herbs, Rhazya stricta and Zingiber officinale, respectively, on the growth of human GBM cell line, U251. R. stricta and Z. officinale are traditionally used in folkloric medicine and have antioxidant, anticarcinogenic, and free radical scavenging properties. Combination of CAERS and CFEZO treatments synergistically suppressed proliferation and colony formation and effectively induced morphological and biochemical features of apoptosis in U251 cells. Apoptosis induction was mediated by release of mitochondrial cytochrome c, increased Bax : Bcl-2 ratio, enhanced activities of caspase-3 and -9, and PARP-1 cleavage. CAERS and CFEZO treatments decreased expression levels of nuclear NF-κBp65, survivin, XIAP, and cyclin D1 and increased expression level of p53, p21, and Noxa. These results suggest that combination of CAERS and CFEZO provides a useful foundation for studying and developing novel chemotherapeutic agents for the treatment of GBM.
机译:迄今为止,在胶质母细胞瘤(GBM)的治疗中已经取得了有限的临床影响。尽管在草药中发现的植物化学物质可以为人类提供新的治疗方法,但单药干预未能在临床试验中带来预期的结果。因此,几种试剂的组合一次获得越来越大的吸引力。在本研究中,我们研究了分别从中草药Rhazya stricta和Zingiber officinale制备的粗生物碱(CAERS)和类黄酮(CFEZO)提取物对人GBM细胞系U251的生长的影响。传统上,R.stricta和Z.officinale用于民俗医学,具有抗氧化,抗癌和清除自由基的特性。 CAERS和CFEZO处理的组合可协同抑制U251细胞的增殖和集落形成,并有效诱导细胞凋亡的形态学和生化特征。凋亡诱导是通过线粒体细胞色素c的释放,Bax:Bcl-2比例的增加,caspase-3和-9活性的增强以及PARP-1的切割介导的。 CAERS和CFEZO处理可降低核NF-κBp65,survivin,XIAP和cyclin D1的表达水平,并提高p53,p21和Noxa的表达水平。这些结果表明,CAERS和CFEZO的组合为研究和开发用于治疗GBM的新型化学治疗剂提供了有用的基础。

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