Study on the expression of epidermal growth factor receptor protein during benzo(a)pyrene induced carcinogenesis
10.3760/cma.j.issn.0253-9624.2017.03.013
- VernacularTitle: 表皮生长因子受体在苯并（a）芘致肺肿瘤中的表达变化
- Author:
Pan GU
1
;
Hailong LIU
;
Yanxia DENG
;
Wei GAO
;
Jianjun LIU
;
Xinfeng HUANG
;
Xiyi LI
;
Haiyan HUANG
Author Information
1. School of Public Health, Guangxi Medical University, Nanning 530021, China
- Publication Type:Journal Article
- Keywords:
Benzo(a)pyrene;
Lung neoplasms;
Epidermal growth factor receptor protein;
16HBE cell
- From:
Chinese Journal of Preventive Medicine
2017;51(3):257-261
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To explore the expression of epidermal growth factor receptor(EGFR) protein during benzo(a)pyrene (BaP) induced carcinogenesis.
Methods:This study, we firstly utilized immunofluorescence assay and Western-blot to examine EGFR expression of the BaP which was constructed previously by project team induced malignant transformation human bronchial epithelial cell (BTC) and the control (16HBE cell). Then, we selected 36 healthy SD rats, divided into two groups according to simple random method, 18 rats each group. The constructed rat lung neoplasm model induced by pulmonary injection of BaP (10 mg/ml of BaP solution in 0.2 ml corn oil), contrast group use 0.2 ml corn oil, lung tissue was collected and the EGFR expression of lung tissue was detected by immunofluorescence assay and Western blot. T analysis was used to test the different of EGFR between two groups.
Results:Immunofluorescence analysis showed that the EGFR expression in BTC was significantly higher than 16HBE cell. Meanwhile, Western blot also was used to confirmed this result, the relative expression of EGFR protein in the rats of the model group the control group were 1.04±0.13 and 2.32±0.12, respectively, and the difference was statistically significance (t=12.39, P<0.001). In vivo, well-defined tumor was found in the rat with pulmonary injection of BaP, and the lung showed diffuse alveolar septal thickening, alveolar wall destruction and pulmonary alveoli fusion, which suggested that the rat lung neoplasm model was constructive successfully. Furthermore, we found the EGFR expression of lung was increased dramatically in the rat lung neoplasm model by immunofluorescence detection and Western blot. The relative expression of EGFR protein in the rats of the model group the control group were 0.21±0.03 and 1.30±0.07, respectively, and the difference was statistically significance (t=12.84, P<0.001).
Conclusion:Expression of EGFR protein was increased during BaP carcinogenesis, and EGFR may play an important role in the carcinogenesis of BaP.
