PM2.5 downregulates MicroRNA-139-5p and induces EMT in Bronchiolar Epithelium Cells by targeting Notch1

被引:19
|
作者
Wang, Yunxia [1 ]
Zhong, Yijue [2 ]
Zhang, Cheng [1 ]
Liao, Jiping [1 ]
Wang, Guangfa [1 ]
机构
[1] Peking Univ, Dept Resp & Crit Care Med, Hosp 1, 8 Xishiku St, Beijing 100034, Peoples R China
[2] Nanjing Med Univ, Affiliated Hosp 1, Dept Geriatr, Jiangsu Prov Hosp, Nanjing, Jiangsu, Peoples R China
来源
JOURNAL OF CANCER | 2020年 / 11卷 / 19期
关键词
PM2.5; 16HBE; EMT; Notch1; miR-139-5p; FINE PARTICULATE MATTER; MESENCHYMAL TRANSITION; LUNG-CANCER; AIR-POLLUTION; IN-VIVO; EXPRESSION; COMPONENTS; EXPOSURE; DISEASES; PATHWAY;
D O I
10.7150/jca.46976
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PM2.5 was closely linked to lung cancer worldwide. However, the mechanism involved in PM2.5 induced lung cancer is still largely unknown. In this study, we performed chronic PM2.5 stimulation animal and cells model to investigate the carcinogenetic mechanisms of PM2.5 by targeting EMT through Notch1 signal pathway. Next, we focused on the miRNA involved in PM2.5 induced Notch1 pathway activation. We found chronic PM2.5 could induce EMT event in vivo and in vitro, while reducing miR-139-5p expression and activating Notch1 pathway meanwhile. And blocking Notch1 signal pathway by specific small molecule inhibitor could reverse PM2.5 induced EMT. Then, overexpression of miR-139-5p downregulated the expression of Notch1 protein in untreated 16HBE cells. Importantly, overexpression of miR-139-5p blocked Notch1 pathway activation and inhibited EMT event in PM2.5 treated cells. These results indicate that PM2.5 induces EMT event through Notch1 signal pathway and miR-139-5p is a novel regulator of PM2.5-induced EMT by targeting Notch1. Our conclusion is that overexpression of miR-139-5p can down-regulate the expression of Notch1 and reverse the occurrence of malignant lung events induced by chronic exposure to PM2.5.
引用
收藏
页码:5758 / 5767
页数:10
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