Qu Zhuling, Song Aiqin, Feng Wei, Teng Ruyang, Gao Jie, Yi Xuanlong
The Affiliated Hospital of Qingdao University Qingdao 266021, Shandong Province, China.
Int J Clin Exp Pathol. 2014 Aug 15;7(9):5888-94. eCollection 2014.
Grandinin (C(46)H(34)O(30)) is a compound found in Melaleuca quinquenervia leaves and in oaks. This study is to determine effects of grandinin on malignant lung cells and the related molecular mechanisms.
Malignant cells were treated with grandinin with various concentrations. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrozolium bromide (MTT) assays and apoptosis assays were performed to determine effects of grandinin on cell viability and apoptosis. Western blotting and real time-PCR were used to determine if grandinin affects levels of phosphorylated EGFR (p-EGFR) and phosphorylated AKT (p-AKT), as well as their mRNA transcript levels.
It was found that grandinin treatments reduce viability of malignant lung cells and induces apoptosis. When treated with grandinin (16 μM), the apoptosis of the three lung cancer cell lines MS-1, A549, and LK-2 were increased by 8-9 folds, in comparison with the cells treated with DMSO only (the control condition). Furthermore, grandinin treatments lead to down-regulation of levels of p-EGFR and p-AKT in three malignant lung cell lines. However, grandinin does not affect mRNA levels of EGFR and AKT.
These experimental results indicated grandinin significantly reduce malignant cell viability and effectively induces apoptosis of malignant lung cells by mediating phosphorylation down-regulation of cellular signaling proteins EGFR and AKT. It is suggested that grandinin treatments might be an effective therapeutic strategy of lung malignancies upon further studies in the future.
格朗宁(C₄₆H₃₄O₃₀)是一种在白千层叶和橡树中发现的化合物。本研究旨在确定格朗宁对恶性肺细胞的影响及其相关分子机制。
用不同浓度的格朗宁处理恶性细胞。进行3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)试验和凋亡试验,以确定格朗宁对细胞活力和凋亡的影响。采用蛋白质免疫印迹法和实时定量聚合酶链反应来确定格朗宁是否影响磷酸化表皮生长因子受体(p-EGFR)和磷酸化蛋白激酶B(p-AKT)的水平及其mRNA转录水平。
发现格朗宁处理可降低恶性肺细胞的活力并诱导凋亡。与仅用二甲基亚砜处理的细胞(对照条件)相比,用格朗宁(16μM)处理时,三种肺癌细胞系MS-1、A549和LK-2的凋亡增加了8至9倍。此外,格朗宁处理导致三种恶性肺细胞系中p-EGFR和p-AKT水平下调。然而,格朗宁不影响EGFR和AKT的mRNA水平。
这些实验结果表明,格朗宁通过介导细胞信号蛋白EGFR和AKT的磷酸化下调,显著降低恶性细胞活力并有效诱导恶性肺细胞凋亡。建议未来进一步研究表明,格朗宁治疗可能是一种有效的肺恶性肿瘤治疗策略。