Wnt信号通路
肺癌
癌症研究
小RNA
肺
生物
细胞生长
癌症
癌
医学
信号转导
肿瘤科
内科学
基因
细胞生物学
遗传学
作者
Jichan Shi,Xieyuan Jiang,Zhijie Yu,Guiqing He,Hongye Ning,Zhengxing Wu,Yuwei Cai,Hehe Yu,Aiqiong Chen
出处
期刊:Tumor Biology
[SAGE]
日期:2015-09-30
卷期号:37 (3): 3051-3057
被引量:20
标识
DOI:10.1007/s13277-015-3949-2
摘要
Lung carcinoma is the most common cancer with increasing morbidity, inefficient therapeutic modality, and poor prognosis, due to the lack of understanding of its related molecular mechanism. ZNRF3 is a newly identified negative regulator of Wnt signaling. In this study, we found that ZNRF3 level is reduced in lung carcinoma compared with normal lung tissue and its expression level is positively correlated with the survival of lung cancer patients. Restoration of ZNRF3 suppressed the proliferation and cell cycle progression of lung cancer cell lines. Suppression of ZNRF3 expression in normal lung cells increased the proliferation rates. In an animal model, ZNRF3 was shown to suppress the growth of lung cancer xenografts. ZNRF3 was shown to negatively regulate the activation of Wnt signaling in lung cancerous and normal cells. Further studies revealed that ZNRF3 is a target of miR-93, an oncogenic microRNA (miRNA) for lung cancer progression. Collectively, we found that miR-93/ZNRF3/Wnt/β-catenin regulatory network contributes to the growth of lung carcinoma. Targeting this pathway may be a promising strategy for lung cancer therapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI