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首页> 外文期刊>Toxicology and Applied Pharmacology >The ethanol extract of Scutellaria baicalensis and the active compounds induce cell cycle arrest and apoptosis including upregulation of p53 and Bax in human lung cancer cells.
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The ethanol extract of Scutellaria baicalensis and the active compounds induce cell cycle arrest and apoptosis including upregulation of p53 and Bax in human lung cancer cells.

机译:黄cut的乙醇提取物和活性化合物诱导人肺癌细胞的细胞周期停滞和凋亡,包括上调p53和Bax。

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摘要

Despite a lack of scientific authentication, Scutellaria baicalensis is clinically used in Chinese medicine as a traditional adjuvant to chemotherapy of lung cancer. In this study, cytotoxicity assays demonstrated that crude ethanolic extracts of S. baicalensis were selectively toxic to human lung cancer cell lines A549, SK-LU-1 and SK-MES-1 compared with normal human lung fibroblasts. The active compounds baicalin, baicalein and wogonin did not exhibit such selectivity. Following exposure to the crude extracts, cellular protein expression in the cancer cell lines was assessed using 2D gel electrophoresis coupled with MALDI-TOF-MS/Protein Fingerprinting. The altered protein expression indicated that cell growth arrest and apoptosis were potential mechanisms of cytotoxicity. These observations were supported by PI staining cell cycle analysis using flow cytometry and Annexin-V apoptotic analysis by fluorescence microscopy of cancer cells treated with the crude extract and pure active compounds. Moreover, specific immunoblotting identification showed the decreased expression of cyclin A results in the S phase arrest of A549 whereas the G(0)/G(1) phase arrest in SK-MES-1 cells results from the decreased expression of cyclin D1. Following treatment, increased expression in the cancer cells of key proteins related to the enhancement of apoptosis was observed for p53 and Bax. These results provide further insight into the molecular mechanisms underlying the clinical use of this herb as an adjuvant to lung cancer therapy.
机译:尽管缺乏科学认证,但黄cut仍在临床上作为中药作为肺癌化疗的传统佐剂在临床上使用。在这项研究中,细胞毒性分析表明,与正常人肺成纤维细胞相比,黄ical的粗乙醇提取物对人肺癌细胞系A549,SK-LU-1和SK-MES-1有选择性毒性。活性化合物黄ical苷,黄ical苷和沃戈宁没有表现出这样的选择性。暴露于粗提物后,使用二维凝胶电泳结合MALDI-TOF-MS /蛋白质指纹图谱评估癌细胞系中细胞蛋白的表达。蛋白质表达的改变表明细胞生长停滞和凋亡是细胞毒性的潜在机制。这些观察结果得到使用粗提物和纯活性化合物处理过的癌细胞的流式细胞术PI染色细胞周期分析和荧光显微镜下膜联蛋白-V凋亡分析的支持。此外,特异性免疫印迹鉴定显示,cyclin A的表达减少导致A549的S期停滞,而SK-MES-1细胞中G(0)/ G(1)的相停导致了cyclin D1的表达减少。治疗后,观察到与p53和Bax凋亡增强有关的关键蛋白在癌细胞中的表达增加。这些结果提供了对这种草药作为肺癌治疗佐剂临床用途的分子机制的进一步了解。

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