Department of Oncology, the Second Affiliated Hospital, Third Military Medical University, 183 Xinqiao main street, Chongqing 400037, China.
BMC Complement Altern Med. 2014 Oct 6;14:377. doi: 10.1186/1472-6882-14-377.
Lung cancers are leading causes of cancer death, and Rumex japonicus has been traditionally used in folk medicine as anti-microorganic, anti-inflammatory and anti-tumor agents. This study was designed to investigate the anti-proliferative activity of physcion 8-O-β-glucopyranoside (PG) isolated from Rumex japonicus Houtt. on A549 cell lines.
In our present study, PG was isolated and identified from the ethanol extracts of R. japonicus. MTT method was used to evaluate the anti-proliferative activity of PG on A549 cell lines, and cell cycle distribution assay, apoptosis assay, and western blot analysis in vitro were used to explore the possible mechanisms.
From the results of our present study, cell viability was obviously inhibited by PG, in a dose- and time-dependent manner. Our results also suggested that the anti-proliferative effect of PG was related to cell cycle arrest at the G2/M phase through repression of cdc2 and Cyclin B1 protein expression. In addition, the results of apoptosis assay and western blot analysis indicated that the anti-proliferative activity could be related to apoptosis via up-regulating the expressions of Bax, caspase-3 and caspase-7, and down-regulating the expressions of Bcl-2.
In conclusion, the PG has significant anti-proliferative activity on A549 cell lines, and the possible mechanism was related to cell cycle arrest at the G2/M phase, and apoptosis via the regulations of Bax, Bcl-2, and caspase-3 and caspase-7.
肺癌是癌症死亡的主要原因,而酸模在民间医学中一直被用作抗微生物、抗炎和抗肿瘤药物。本研究旨在研究从酸模中分离出的大黄素 8-O-β-吡喃葡萄糖苷(PG)对 A549 细胞系的抗增殖活性。
在本研究中,PG 是从酸模的乙醇提取物中分离和鉴定出来的。MTT 法用于评估 PG 对 A549 细胞系的抗增殖活性,体外细胞周期分布分析、凋亡分析和 Western blot 分析用于探讨可能的机制。
从本研究的结果来看,PG 以剂量和时间依赖的方式明显抑制细胞活力。我们的结果还表明,PG 的抗增殖作用与通过抑制 cdc2 和 Cyclin B1 蛋白表达使细胞周期停滞在 G2/M 期有关。此外,凋亡分析和 Western blot 分析的结果表明,抗增殖活性可能与通过上调 Bax、caspase-3 和 caspase-7 的表达以及下调 Bcl-2 的表达而导致的细胞凋亡有关。
总之,PG 对 A549 细胞系具有显著的抗增殖活性,其可能的机制与细胞周期停滞在 G2/M 期以及 Bax、Bcl-2 和 caspase-3 和 caspase-7 的调节有关的凋亡有关。