Cheng Hui, Wang Yun-Long, Su Jing-Jing, Hu Rong-Feng, Li Qing-Lin
Key Laboratory of Xin'an Medicine, Ministry of Education, Anhui University of Chinese Medicine, Hefei 230038, China.
Zhongguo Zhong Yao Za Zhi. 2018 Nov;43(21):4311-4316. doi: 10.19540/j.cnki.cjcmm.20180601.001.
The aim of this paper was to observe the effect of gambogenic acid on angiogenesis of lung cancer and its preliminary mechanism. After culturing lung adenocarcinoma A549 cells, the conditioned medium was treated with gambogenic acid and then used to culture human umbilical vein endothelial cells (HUVECs) to establish the indirect contact cell co-culture system. A two-dimensional culture model of HUVEC was established with matrigel to observe the effect of gambogenic acid on angiogenesis. DAPI staining was used to observe the morphological changes in HUVEC cells after treatment with gambogenic acid under the fluorescence microscope. Annexin V-FITC/PI staining and flow cytometry analysis were used to determine gambogenic acid's effect on HUVEC cell apoptosis rate. The protein expressions of PI3K, p-PI3K, Akt, p-Akt were measured by Western blot. PTEN-siRNA was transfected into cells, and RT-PCR was used to detect the expression levels of PI3K and Akt genes. Gambogenic acid can significantly inhibit angiogenesis, and its inhibitory effect was dose-dependent. DAPI staining showed apoptotic morphological features of HUVEC cells under fluorescence microscope. Annexin V-FITC/PI staining showed that gambogenic acid induced apoptosis in HUVECs. The results of Western blot showed that the expressions of p-PI3K and p-Akt protein were down-regulated with gambogenic acid, while the expressions of PI3K and Akt protein was insignificant. The results of RT-PCR indicated that the expressions of PI3K and Akt protein were up-regulated by PTEN siRNA. Gambogenic acid can inhibit angiogenesis in lung cancer in vitro, and the mechanism of inhibiting angiogenesis may be related to the PI3K/Akt signaling pathway.
本文旨在观察藤黄酸对肺癌血管生成的影响及其初步机制。培养肺腺癌A549细胞后,用藤黄酸处理条件培养基,然后用于培养人脐静脉内皮细胞(HUVECs),建立间接接触细胞共培养体系。用基质胶建立HUVEC的二维培养模型,观察藤黄酸对血管生成的影响。采用DAPI染色在荧光显微镜下观察藤黄酸处理后HUVEC细胞的形态变化。采用Annexin V-FITC/PI染色和流式细胞术分析测定藤黄酸对HUVEC细胞凋亡率的影响。通过Western blot检测PI3K、p-PI3K、Akt、p-Akt的蛋白表达。将PTEN-siRNA转染到细胞中,用RT-PCR检测PI3K和Akt基因的表达水平。藤黄酸可显著抑制血管生成,且其抑制作用呈剂量依赖性。DAPI染色显示荧光显微镜下HUVEC细胞具有凋亡形态特征。Annexin V-FITC/PI染色显示藤黄酸诱导HUVEC细胞凋亡。Western blot结果显示,藤黄酸使p-PI3K和p-Akt蛋白表达下调,而PI3K和Akt蛋白表达无明显变化。RT-PCR结果表明,PTEN siRNA使PI3K和Akt蛋白表达上调。藤黄酸可在体外抑制肺癌血管生成,其抑制血管生成的机制可能与PI3K/Akt信号通路有关。