Integrin αv promotes proliferation by activating ERK 1/2 in the human lung cancer cell line A549

被引:10
作者
Fu, Shijie [1 ]
Fan, Limin [1 ]
Pan, Xufeng [1 ]
Sun, Yifeng [1 ]
Zhao, Heng [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Thorac Surg, Shanghai 200030, Peoples R China
关键词
integrin alpha v; A549; cells; ERK; 1/2; proliferation; apoptosis; MESENCHYMAL-TRANSITION; PROGNOSTIC-FACTOR; ALPHA-V-BETA-6; METASTASIS; GROWTH; TRANSDUCTION; EXPRESSION; UROKINASE; INVASION;
D O I
10.3892/mmr.2014.2860
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer is a leading cause of cancer-related death worldwide, and non-small cell lung cancer (NSCLC) constitutes similar to 85% of lung cancers. However, the mechanisms underlying the progression of NSCLC remain unclear. In this study, we found the mRNA and protein expression levels of integrin alpha v are both increased in NSCLC tissues compared to healthy ones, which indicates that integrin alpha v may play an important role in NSCLC progression. To further investigate the roles of integrin alpha v in NSCLC, we overexpressed the integrin alpha v gene in the NSCLC cell line A549, and found that the cell proliferative ability increased. The apoptosis of A549 cells was inhibited with overexpression of integrin alpha v. To elucidate the molecular mechanism underlying the role of integrin alpha v in promoting NSCLC progression, we studied the expression of proteins from a number of important pathways associated with tumorigenesis, and found that the extracellular signal regulated protein kinase (ERK)1/2 signaling pathway may be involved in the mediation of the observed integrin alpha v effects. component of an important pathway for tumorigenesis, the ERK 1/2. Following inhibition of ERK 1/2 signaling, the proliferation of A549 cells induced by integrin alpha v was reduced, while the inhibition of apoptosis was attenuated. Our findings demonstrate that integrin av promotes the proliferation of the human lung cancer cell line A549 by activating the ERK 1/2 signaling pathway, which suggests that this pathway may be a promising target for the treatment of human lung cancer.
引用
收藏
页码:1266 / 1271
页数:6
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