Huang Jie, Chen Shi, Shi Yi, Li Cheng-Hong, Wang Xiao-Jiang, Li Fa-Jiu, Wang Chuan-Hai, Meng Qing-Hua, Zhong Jin-Nan, Liu Min, Wang Zi-Ming
Department of Respiratory Medicine, Wuhan No.6 Hospital, Affiliated Hospital of Jianghan University, Wuhan, 430015, PR China.
J BUON. 2017 Nov-Dec;22(6):1422-1427.
Green tea (Camellia sinensis) is considered as a rich source of epigallocatechin gallate (EGCG) which has been shown to exert impressive pharmacological properties. The anticancer properties of EGCG have been extensively studied however, its anticancer activity has not been explored in lung cancer. The present study was therefore designed to evaluate the anticancer effects of EGCG against non-small cell lung cancer (NSCLC) cell line A-549 and normal human fibroblast FR-2 cells.
Cell viability was assessed by CCK8 assay, apoptosis by DAPI, annexin V/propidium iodide (PI) and flowcytometery and cell cycle analysis by flow cytometry. Cell migration capacity was investigated by wound-healing assay and protein expression was examined by Western blotting.
The results revealed that EGCC could inhibit the proliferation of A-549 cells in a concentration-dependent manner and exhibited an IC50 of 25 μM against the IC50 of 100 μM against the normal human fibroblasts. Further evaluation revealed that EGCG exerts its anticancer effects via induction of apoptosis, modulation of Bax/blc-2 ratio and by triggering G2/M cell cycle arrest. Furthermore, EGCG could also inhibit the migration of A5-49 cells in a concentration-dependent manner.
In conclusion, based on our results, we believe that EGCG could prove to be an important lead molecule for the treatment of lung cancer.
绿茶(茶树)被认为是表没食子儿茶素没食子酸酯(EGCG)的丰富来源,EGCG已被证明具有显著的药理特性。EGCG的抗癌特性已得到广泛研究,然而,其在肺癌中的抗癌活性尚未得到探索。因此,本研究旨在评估EGCG对非小细胞肺癌(NSCLC)细胞系A-549和正常人成纤维细胞FR-2细胞的抗癌作用。
通过CCK8法评估细胞活力,通过DAPI、膜联蛋白V/碘化丙啶(PI)和流式细胞术检测细胞凋亡,并通过流式细胞术进行细胞周期分析。通过伤口愈合试验研究细胞迁移能力,并通过蛋白质印迹法检测蛋白质表达。
结果显示,EGCG能以浓度依赖性方式抑制A-549细胞的增殖,对A-549细胞的IC50为25μM,而对正常人成纤维细胞的IC50为100μM。进一步评估表明,EGCG通过诱导细胞凋亡、调节Bax/bcl-2比值以及触发G2/M期细胞周期阻滞发挥其抗癌作用。此外,EGCG还能以浓度依赖性方式抑制A5-49细胞的迁移。
总之,基于我们的研究结果,我们认为EGCG可能被证明是治疗肺癌的重要先导分子。