Zhou Yehan, Ye Xiufeng, Shi Yao, Wang Ke, Wan Dan
Basic Medicine College, Chongqing Medical University, Chongqing 400016, China.
Basic Medicine College, Chongqing Medical University, Chongqing 400016, China. *Corresponding author, E-mail:
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2016 Feb;32(2):173-6.
To explore the effect of grape seed proanthocyanidins (GSPs) on the invasion and migration of A549 lung cancer cells and the underlying mechanism.
Trypan blue dye exclusion assay was used to determine the cytotoxic effect of varying doses of GSPs on the BEAS-2B normal human pulmonary epithelial cells. After treated with 0, 10, 20, 40, 80 μg/mL GSP, the proliferation of A549 cells was detected by MTT assay; the invasion and migration of A549 cells were determined by Transwell(TM) assay and scratch wound assay, respectively. The levels of epithelial growth factor receptor (EGFR), E-cadherin, N-cadherin in A549 cells treated with GSPs were detected by Western blotting.
(0-40) μg/mL GSPs had no significant toxic effect on BEAS-2B cells, while 80 μg/mL GSPs had significant cytotoxicity to BEAS-2B cells. The proliferation of A549 cells was significantly inhibited within limited dosage in a dose-dependent manner, and the abilities of invasion and migration of A549 cells were also inhibited. Western blotting showed that the expression of EGFR and N-cadherin decreased, while E-cadherin increased after GSPs treatment.
GSPs could inhibit the abilities of proliferation, invasion and migration of A549 cells, which might be related to the dow-regulation of EGFR and N-cadherin and the up-regulation of E-cadherin.
探讨葡萄籽原花青素(GSPs)对A549肺癌细胞侵袭和迁移的影响及其潜在机制。
采用台盼蓝拒染法测定不同剂量GSPs对BEAS-2B正常人肺上皮细胞的细胞毒性作用。用0、10、20、40、80μg/mL GSP处理后,采用MTT法检测A549细胞的增殖情况;分别采用Transwell(TM)法和划痕试验测定A549细胞的侵袭和迁移能力。通过蛋白质免疫印迹法检测经GSPs处理的A549细胞中表皮生长因子受体(EGFR)、E-钙黏蛋白、N-钙黏蛋白的水平。
(0-40)μg/mL GSPs对BEAS-2B细胞无明显毒性作用,而80μg/mL GSPs对BEAS-2B细胞具有明显的细胞毒性。在有限剂量范围内,A549细胞的增殖受到显著抑制,且呈剂量依赖性,同时A549细胞的侵袭和迁移能力也受到抑制。蛋白质免疫印迹法显示,GSPs处理后,EGFR和N-钙黏蛋白的表达降低,而E-钙黏蛋白的表达增加。
GSPs可抑制A549细胞的增殖、侵袭和迁移能力,这可能与EGFR和N-钙黏蛋白的下调以及E-钙黏蛋白的上调有关。