Liang Dandan, Wang Chunmiao, Li Junying, Qin Liangshu, Su Zhengying, Hou Huaxin
Department of Pharmaceutical Analysis, Guangxi Medical University, Nanning 530021, China.
Department of Pharmacy, Guangxi International Zhuang Medicine Hospital, Nanning 530201, China.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2020 Oct;36(10):918-923.
Objective To establish a triple negative breast cancer cell line stably expressing human epidermal growth factor receptor (EGFR) promoter and luciferase (Luc) reporter gene and to preliminarily verify its application. Methods Using genetic recombination technology, the lentiviral vector carrying Luc reporter and EGFR promoter sequence was designed and constructed to infect MDA-MB231 cells and obtain MDA-MB231-EGFR-Luc2 cell lines by the selection with puromycin. The Luc luminescence value after stimulating with EGFR activator EGF or inhibitor gefitinib regulating the EGFR promoter activities was detected. Results Gene sequencing and enzyme digestion verified that the lentiviral expression vector carrying Luc reporter vector recombined with EGFR promoter was successfully constructed. Lentivirus-infected MDA-MB231 cells were screened by puromycin, the MDA-MB231-EGFR-Luc2 cells stably expressing firefly Luc was obtained. EGF increased the Luc luminescence value of MDA-MB231-EGFR-Luc2 cells in a dose-dependent manner, while gefitinib did the opposite. Conclusion The cell line of MDA-MB231-EGFR-Luc2 containing EGFR promoter and Luc reporter gene has been successfully constructed, which provides a new cell model for high throughput screening of EGFR-targeting drugs.
目的 建立稳定表达人表皮生长因子受体(EGFR)启动子和荧光素酶(Luc)报告基因的三阴性乳腺癌细胞系,并初步验证其应用。方法 利用基因重组技术,设计构建携带Luc报告基因和EGFR启动子序列的慢病毒载体,感染MDA-MB231细胞,经嘌呤霉素筛选获得MDA-MB231-EGFR-Luc2细胞系。检测EGFR激活剂表皮生长因子(EGF)或抑制剂吉非替尼调控EGFR启动子活性后Luc的发光值。结果 基因测序和酶切验证成功构建了携带Luc报告载体并与EGFR启动子重组的慢病毒表达载体。经嘌呤霉素筛选慢病毒感染的MDA-MB231细胞,获得稳定表达萤火虫Luc的MDA-MB231-EGFR-Luc2细胞。EGF呈剂量依赖性增加MDA-MB231-EGFR-Luc2细胞的Luc发光值,而吉非替尼则相反。结论 成功构建了含EGFR启动子和Luc报告基因 的MDA-MB231-EGFR-Luc2细胞系,为EGFR靶向药物的高通量筛选提供了新的细胞模型。