Bone morphogenetic protein-4 induced by NDRG2 expression inhibits MMP-9 activity in breast cancer cells

被引:81
作者
Shon, Soo-Kyung
Kim, Aeyung
Kim, Ji Young
Kim, Keun Il
Yang, Young
Lim, Jong-Seok [1 ]
机构
[1] Sookmyung Womens Univ, Dept Biol Sci, Seoul 140742, South Korea
关键词
Breast cancer; NDRG2; BMP-4; MMP; Migration; Invasion; CARCINOMA-CELLS; PROLIFERATION; ACTIVATION; ANGIOGENESIS; SUPPRESSOR; APOPTOSIS; SURVIVAL; INVASION; FAMILY; GROWTH;
D O I
10.1016/j.bbrc.2009.05.038
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 the current study, we examined the function of N-myc downstream-regulated gene 2 (NDRG2) expression in breast cancer cells, especially focusing on the role of bone morphogenetic protein-4 (BMP-4) induced by NDRG2. NDRG2 expression in MDA-MB-231 cells inhibited the mRNA expression of several matrix metalloproteinases (MMPs) and the gelatinolytic activity of MMP-9. Interestingly, a specific induction of active BMP-4 was exclusively observed in MDA-MB-231-NDRG2 cells but not in MDA-MB-231-mock cells. Neutralization of BMP-4 in MDA-MB-231-NDRG2 cells resulted in the rescue of MMP-9 mRNA expression and migration capacity. In addition, treatment with recombinant BMP-4 dramatically suppressed MMP-9 mRNA expression, gelatinolytic MMP-9 activity, migration, and invasion capacity both in MDA-MB-231 and PMA-treated MCF-7 cells. Collectively, our data show that BMP-4 induced by NDRG2 expression inhibits the metastatic potential of breast cancer cells, especially via suppression of MMP-9 activity. (C) 2009 Elsevier Inc. All rights reserved
引用
收藏
页码:198 / 203
页数:6
相关论文
共 26 条
[1]   Expression of NDRG2 is related to tumor progression and survival of gastric cancer patients through Fas-mediated cell death [J].
Choi, Seung-Chul ;
Yoon, Suk Ran ;
Park, Yuk Pheel ;
Song, Eun Young ;
Kim, Jae Wha ;
Kim, Woo Ho ;
Yang, Young ;
Lim, Jong-Seok ;
Lee, Hee Gu .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2007, 39 (06) :705-714
[2]   Bone morphogenetic protein-6 promotes osteoblastic prostate cancer bone metastases through a dual mechanism [J].
Dai, JL ;
Keller, J ;
Zhang, J ;
Lu, Y ;
Yao, Z ;
Keller, ET .
CANCER RESEARCH, 2005, 65 (18) :8274-8285
[3]   Bone morphogenetic protein-4 is overexpressed in colonic adenocarcinomas and promotes migration and invasion of HCT116 cells [J].
Deng, Haiyun ;
Makizumi, Ryouji ;
Ravikumaya, T. S. ;
Dong, Huali ;
Yang, Wancai ;
Yang, Weng-Lang .
EXPERIMENTAL CELL RESEARCH, 2007, 313 (05) :1033-1044
[4]   PI3K/Akt-Dependent Transcriptional Regulation and Activation of BMP-2-Smad Signaling by NF-κB in Metastatic Prostate Cancer Cells [J].
Graham, Tisheeka R. ;
Odero-Marah, Valerie A. ;
Chung, Leland W. ;
Agrawal, Krishna C. ;
Davis, Rodney ;
Abdel-Mageed, Asim B. .
PROSTATE, 2009, 69 (02) :168-180
[5]  
Hanemaaijer R, 2000, INT J CANCER, V86, P204, DOI 10.1002/(SICI)1097-0215(20000415)86:2<204::AID-IJC9>3.0.CO
[6]  
2-6
[7]   Bone morphogenetic protein-4 inhibits proliferation and induces apoptosis of multiple myeloma cells [J].
Hjertner, Ö ;
Hjorth-Hansen, H ;
Börset, M ;
Seidel, C ;
Waage, A ;
Sundan, A .
BLOOD, 2001, 97 (02) :516-522
[8]   Bone morphogenetic proteins in development [J].
Hogan, BLM .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1996, 6 (04) :432-438
[9]  
Hu XL, 2004, WORLD J GASTROENTERO, V10, P3518
[10]  
Ide H, 1997, CANCER RES, V57, P5022