ADAM15 targets MMP9 activity to promote lung cancer cell invasion

被引:44
作者
Dong, Dan-Dan [1 ]
Zhou, Hui [2 ]
Li, Gao [3 ]
机构
[1] Sichuan Acad Med Sci, Sichuan Prov Peoples Hosp, Dept Pathol, Chengdu 610072, Sichuan, Peoples R China
[2] Cent S Univ, Affiliated Canc Hosp Xiangya, Sch Med, Dept Thorac Surg, Changsha 410013, Hunan, Peoples R China
[3] Hainan Gen Hosp, Dept Thorac Surg, Haikou 570311, Hainan, Peoples R China
关键词
non-small cell lung cancer; A disintegrin and metalloproteinase; matrix metalloproteinase 9; metastasis; cell migration; GROWTH-FACTOR RECEPTOR; E-CADHERIN; TUMOR-GROWTH; EXPRESSION; DISINTEGRIN; PROSTATE; METALLOPROTEINASES; METASTASIS; PATHWAY; MATRIX-METALLOPROTEINASE-9;
D O I
10.3892/or.2015.4203
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
ADAM15 is a membrane-associated proteinase belonging to a disintegrin and metalloproteinase (ADAM) family. Recent studies suggested that ADAM15 is overexpressed in several types of cancer and is involved in metastatic tumor progression. However, the function of ADAM15 in non-small cell lung cancer (NSCLC) is currently unknown. In the present study, we found that high expression of ADAM15 was associated with decreased overall survival (OS) and disease-free survival (DFS) in NSCLC patients. Furthermore, shRNA-mediated knockdown of ADAM15 attenuated cell migration and invasion. Mechanistic study demonstrated that ADAM15 upregulated MMP9 expression in lung cancer cells via activation of the MEK-ERK pathway. Moreover, ADAM 15 proteolytically cleaved and activated pro-MMP9 in vitro and interacted with MMP9 in vivo. Overexpression of ADAM15 in A549 cells promoted cell invasion, while knocking down MMP9 attenuated cell invasive ability. Therefore, our data not only support a pro-metastatic role of ADAM 15 in lung cancer progression, but also reveal a novel mechanism of ADAM15 in promoting cancer cell invasion through directly targeting MMP9 activation.
引用
收藏
页码:2451 / 2460
页数:10
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