Blocking platelet-derived growth factor-d inhibits human lung cancer progression

被引:0
作者
Huang, Feng [1 ]
Yao, Yongliang [1 ]
Wu, Jianhong [1 ]
Zhang, Yanqing [1 ]
Yu, Liya [1 ]
Pu, Xiongyong [1 ]
Xia, Longfei [2 ]
机构
[1] Jiangsu Univ, Peoples Hosp Kunshan 1, Dept Clin Lab, Suzhou, Jiangsu, Peoples R China
[2] Jiangsu Univ, Sch Med, 301 Xuefu Rd, Zhenjiang 212013, Jiangsu, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2017年 / 10卷 / 03期
关键词
Lung cancer; PDGF-D; siRNA; cancer growth; migration; invasion; EPITHELIAL-MESENCHYMAL TRANSITION; PDGF-D; CELL-PROLIFERATION; EMERGING ROLES; TUMOR-GROWTH; EXPRESSION; PATHWAY; OVEREXPRESSION; METASTASIS; RESISTANCE;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Platelet-derived growth factor-D (PDGF-D) is a kind of growth chemokine that regulates tumor growth and metastasis in various cancers. However, the function of this gene in lung cancer is little known. Here we found that PDGF-D is overexpressed in lung cancer tissue compared to adjacent tissue. Interestingly, the serum levels of PDGFD in lung cancer patients were significantly decreased after operation. Knockdown of PDGF-D using siRNA in lung cancer cells inhibits cell proliferation in vitro and in vivo and decreased the activation of p-AKT signaling pathway. Moreover, silencing of PDGF-D in A549 cells remarkably reduced cell migration and invasion. Furthermore, PDGF-D knockdown significantly increased E-cadherin expression but decreased the expression of N-cadherin, MMP-2 and MMP-9. Taken together, our findings indicate that PDGF-D is involved in the progression of lung cancer growth, migration and invasion. Targeting PDGF-D with siRNA may provide a novel strategy for lung cancer therapy in patients with over-expressed PDGF-D.
引用
收藏
页码:3109 / 3115
页数:7
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