KiSS1 inhibits growth and invasion of osteosarcoma cells through inhibition of the MAPK pathway

被引:23
|
作者
Zhang, Y. [1 ]
Tang, Y. J. [1 ]
Li, Z. H. [1 ]
Pan, F. [1 ]
Huang, K. [1 ]
Xu, G. H. [1 ]
机构
[1] Zhabei Dist Cent Hosp, Dept Orthoped, Shanghai 200070, Peoples R China
来源
EUROPEAN JOURNAL OF HISTOCHEMISTRY | 2013年 / 57卷 / 04期
关键词
KiSS1; osteosarcoma; growth; invasion; METASTASIS SUPPRESSOR; BLADDER-CANCER; EXPRESSION; PROGNOSIS; CARCINOMA; MARKERS;
D O I
10.4081/ejh.2013.e30
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
As a metastasis suppressor, KiSS1 has been implicated in numerous human cancers. However, recent studies have demonstrated that KiSS1 promotes tumor growth and metastasis in breast cancer, and it is unclear about the expression and function of KiSS1 in human osteosarcoma (OS). The aim of the present study was to investigate the role and molecular mechanisms of KiSS1 in human OS. The expression of KiSS1 was assessed by immunohistochemical assay using a tissue microarray procedure in forty cases of OS tissues. A gain-of-function approach was used to observe the effects of lentiviral vector-mediated overexpression of KiSS1 (Lv-KiSS1) on the biological behaviors including proliferative activities and invasive potential of OS MG-63 cells, indicated by MTT and Transwell assays, respectively. The results showed that the expression of KiSS1 protein in OS tissues was significantly lowered compared to that in adjacent non-cancerous tissues (42.5% vs 70.0%, P=0.023), and had negative correlation with distant metastases of the tumor (P=0.019). Overexpression of KiSS1 inhibited proliferation and invasion of OS cells with the decreased expression of p38 MAPK and matrix metalloproteinase-9 (MMP-9). Taken together, our findings indicate that the decreased expression of KiSS1 is correlated with distant metastasis of OS, and KiSS1 may function as a tumor suppressor in OS cells through inhibition of the MAPK pathway, suggesting that KiSS1 may serve as a potential therapeutic target for the treatment of cancer.
引用
收藏
页码:199 / 204
页数:6
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