The E-cadherin-repressed hNanos1 gene induces tumor cell invasion by upregulating MT1-MMP expression

被引:28
作者
Bonnomet, A. [1 ,2 ]
Polette, M. [1 ]
Strumane, K. [3 ,4 ]
Gilles, C. [2 ]
Dalstein, V. [1 ]
Kileztky, C. [1 ]
Berx, G. [3 ]
van Roy, F. [3 ]
Birembaut, P. [1 ]
Nawrocki-Raby, B. [1 ]
机构
[1] Univ Reims, Histol Lab, CHU Maison Blanche, IFR 53,INSERM UMRS 514, F-51100 Reims, France
[2] Univ Liege, CHU Sart Tilman, Lab Dev & Tumor Biol, Liege, Belgium
[3] Univ Ghent VIB, Dept Mol Biomed Res, B-9052 Ghent, Belgium
[4] Leiden Univ, Med Ctr, Dept IHB, Leiden, Netherlands
关键词
hNanos1; E-cadherin; MT1-MMP; cancer; cell invasion;
D O I
10.1038/sj.onc.1211035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, we examined the role of the E-cadherin-repressed gene human Nanos1 (hNanos1) in tumor invasion process. First, our in vivo study revealed that hNanos1 mRNAs were overexpressed in invasive lung carcinomas. Moreover, hNanos1 was co-localized with MT1-MMP (membrane type 1-matrix metalloproteinase) in E-cadherin-negative invasive lung tumor clusters. Using an inducible Tet-on system, we showed that induction of hNanos1 expression in DLD1 cells increased their migratory and invasive abilities in a three-dimensional migration and in a modified Boyden chamber assay. Accordingly, we demonstrated that hNanos1 upregulated MT1-MMP expression at the mRNA and protein levels. Inversely, using an RNA interference strategy to inhibit hNanos1 expression in invasive Hs578T, BT549 and BZR cancer cells, we observed a downregulation of MT1-MMP mRNA and protein and concomitantly a decrease of the invasive capacities of tumor cells in a modified Boyden chamber assay. Taken together, our results demonstrate that hNanos1, by regulating MT1-MMP expression, plays an important role in the acquisition of invasive properties by epithelial tumor cells.
引用
收藏
页码:3692 / 3699
页数:8
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