Zhang Hua, Cao Yumei, Chen Yuru, Li Guangxi, Yu Hanshu
Department of Interventional Radiology, Heze Municipal Hospital, Heze, Shandong 274000, P.R. China.
Heze Municipal Hospital, Heze, Shandong 274000, P.R. China.
Oncol Lett. 2018 Apr;15(4):5739-5743. doi: 10.3892/ol.2018.8031. Epub 2018 Feb 12.
The present study investigated the inhibitory effects of apatinib on the proliferation of the SMMC-7721 hepatocellular carcinoma cell line to explore the possible mechanism. The MTT assay was used to detect the inhibitory effects of the different concentrations of apatinib on the proliferation of SMMC-7721 cells. Annexin V/PI double staining was performed to investigate the effects of apatinib on the apoptosis of SMMC-7721 cells. Expression of the apoptosis-related genes and after apatinib treatment was detected by reverse transcription-quantitative PCR (RT-qPCR) and western blot analysis. Expression of the PI3K, p-PI3K, Akt and p-Akt proteins after apatinib treatment was detected using western blot analysis. The MTT results showed that apatinib inhibited the proliferation of SMMC-7721 cells. Annexin V/PI double staining showed that apatinib induced the apoptosis of SMMC-7721 cells in a concentration-dependent manner. Results of RT-qPCR and western blot analysis showed that apatinib was able to induce the expression of pro-apoptotic genes and and inhibited the expression of anti-apoptotic gene . In addition, the western blot analysis revealed that p-PI3K and p-Akt was significantly decreased following apatinib treatment, while no significant differences were found in the total protein levels of PI3K and Akt. The results of the present show that apatinib is capable of promoting the apoptosis of SMMC-7721 cells by inhibiting the PI3K/Akt signal transduction pathway, upregulating the expression of pro-apoptotic genes and , and downregulating the expression level of the anti-apoptotic gene .
本研究探讨了阿帕替尼对SMMC - 7721肝癌细胞系增殖的抑制作用,以探索其可能的机制。采用MTT法检测不同浓度阿帕替尼对SMMC - 7721细胞增殖的抑制作用。进行Annexin V/PI双染以研究阿帕替尼对SMMC - 7721细胞凋亡的影响。通过逆转录定量PCR(RT - qPCR)和蛋白质印迹分析检测阿帕替尼处理后凋亡相关基因的表达。使用蛋白质印迹分析检测阿帕替尼处理后PI3K、p - PI3K、Akt和p - Akt蛋白的表达。MTT结果显示阿帕替尼抑制SMMC - 7721细胞的增殖。Annexin V/PI双染显示阿帕替尼以浓度依赖的方式诱导SMMC - 7721细胞凋亡。RT - qPCR和蛋白质印迹分析结果表明,阿帕替尼能够诱导促凋亡基因的表达并抑制抗凋亡基因的表达。此外,蛋白质印迹分析显示阿帕替尼处理后p - PI3K和p - Akt显著降低,而PI3K和Akt的总蛋白水平无显著差异。本研究结果表明,阿帕替尼能够通过抑制PI3K/Akt信号转导通路、上调促凋亡基因的表达以及下调抗凋亡基因的表达水平来促进SMMC - 7721细胞凋亡。