Medicines Research Group, School of Health and Bioscience, University of East London, Stratford, London E15 4LZ, UK.
Toxicol Appl Pharmacol. 2011 Aug 1;254(3):221-8. doi: 10.1016/j.taap.2011.03.016. Epub 2011 Mar 30.
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.
尽管缺乏科学验证,黄芩仍被临床用于中医,作为肺癌化疗的传统辅助药物。在这项研究中,细胞毒性检测表明,黄芩的粗醇提取物对人肺癌细胞株 A549、SK-LU-1 和 SK-MES-1 具有选择性毒性,而对正常肺成纤维细胞则没有这种选择性。黄芩苷、黄芩素和汉黄芩素等活性化合物则没有这种选择性。在用粗提取物处理后,通过 2D 凝胶电泳与 MALDI-TOF-MS/蛋白质指纹图谱联用,评估了癌细胞系中的细胞蛋白表达。改变的蛋白表达表明细胞生长停滞和细胞凋亡可能是细胞毒性的潜在机制。这些观察结果得到了用粗提取物和纯活性化合物处理的癌细胞的 PI 染色细胞周期分析和流式细胞术检测以及荧光显微镜下 Annexin-V 凋亡分析的支持。此外,特定的免疫印迹鉴定表明,cyclin A 的表达减少导致 A549 细胞在 S 期停滞,而 SK-MES-1 细胞中的 G(0)/G(1)期停滞则是由于 cyclin D1 的表达减少所致。治疗后,观察到与促进细胞凋亡相关的关键蛋白在癌细胞中的表达增加,包括 p53 和 Bax。这些结果为该草药作为肺癌治疗辅助药物的临床应用的分子机制提供了进一步的深入了解。