N-Acetylglucosaminyltransferase V triggers overexpression of MT1-MMP and reinforces the invasive/metastatic potential of cancer cells

被引:11
作者
Lee, Ju Hee [1 ]
Kang, Jeong Gu [1 ]
Song, Kyoung Jin [1 ]
Jeon, Seong Kook [1 ]
Oh, Sejeong [2 ]
Kim, Yong-Sam [1 ]
Ko, Jeong-Heon [1 ]
机构
[1] Korea Res Inst Biosci & Biotechnol, Canc Biomarkers Dev Res Ctr, Taejon, South Korea
[2] Catholic Univ Korea, Coll Med, Dept Surg, Inchon 403720, South Korea
关键词
GnT-V; MMP-2; MT1-MMP; Tumor progression; TYPE-1; MATRIX-METALLOPROTEINASE; COLON-CANCER; ABERRANT GLYCOSYLATION; TUMOR INVASION; EXPRESSION; ACTIVATION; METASTASIS; CARCINOMA; MIGRATION; GROWTH;
D O I
10.1016/j.bbrc.2013.01.065
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
N-Acetylglucosaminyltransferase V (GnT-V) is an enzyme that catalyzes the formation of a beta 1,6-N-acetylglucosamine (GlcNAc) side chain to a core mannosyl residue in N-linked glycoproteins. Besides its direct function of producing aberrant glycoproteins, it promotes cancer progression by its involvement in the stimulation of oncoproteins. Herein, we report that GnT-V guided the transcriptional activation of membrane-type matrix metalloproteinase-1 (MT1-MMP) in cancer cells. The activated MT1-MMP expression had dual effects on cancer progression. It not only promoted proteolytic activity for cancer cells per se, but also led to the activation of MMP-2. Consequently, the activation of the two MMPs triggered by GnT-V intensified the invasive potential. A quantitative analysis using clinical tissues revealed a relatively strong correlation between GnT-V overexpression and MT1-MMP upregulation. In this study, we report for the first time that GnT-V directs cancer progression by modulating MMPs in cancer. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:658 / 663
页数:6
相关论文
共 28 条
[1]   The inactive 44-kDa processed form of membrane type 1 matrix metalloproteinase (MT1-MMP) enhances proteolytic activity via regulation of endocytosis of active MT1-MMP [J].
Cho, Jin-Ah ;
Osenkowski, Pamela ;
Zhao, Huiren ;
Kim, Seaho ;
Toth, Marta ;
Cole, Kristina ;
Aboukameel, Amro ;
Saliganan, Allen ;
Schuger, Lucia ;
Bonfil, R. Daniel ;
Fridman, Rafael .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (25) :17391-17405
[2]   BETA-1-6 BRANCHING OF ASN-LINKED OLIGOSACCHARIDES IS DIRECTLY ASSOCIATED WITH METASTASIS [J].
DENNIS, JW ;
LAFERTE, S ;
WAGHORNE, C ;
BREITMAN, ML ;
KERBEL, RS .
SCIENCE, 1987, 236 (4801) :582-585
[3]   Cancer Invasion and the Microenvironment: Plasticity and Reciprocity [J].
Friedl, Peter ;
Alexander, Stephanie .
CELL, 2011, 147 (05) :992-1009
[4]  
Gingras D., 2010, BIOCHIM BIOPHYS ACTA, P142
[5]  
Granovsky M, 2000, NAT MED, V6, P306
[6]  
Guo HB, 2002, CANCER RES, V62, P6837
[7]   The hallmarks of cancer [J].
Hanahan, D ;
Weinberg, RA .
CELL, 2000, 100 (01) :57-70
[8]   Regulation of membrane type-matrix metalloproteinases [J].
Hernandez-Barrantes, S ;
Bernardo, M ;
Toth, M ;
Fridman, R .
SEMINARS IN CANCER BIOLOGY, 2002, 12 (02) :131-138
[9]   Prometastatic effect of N-acetylglucosaminyltransferase V is due to modification and stabilization of active matriptase by adding β1-6 GlcNAc branching [J].
Ihara, S ;
Miyoshi, E ;
Ko, JH ;
Murata, K ;
Nakahara, S ;
Honke, K ;
Dickson, RB ;
Lin, CY ;
Taniguchi, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (19) :16960-16967
[10]   Expression of membrane-type matrix metalloproteinase-1 in human pancreatic adenocarcinomas [J].
Imamura, T ;
Ohshio, G ;
Mise, M ;
Harada, T ;
Suwa, H ;
Okada, N ;
Wang, ZH ;
Yoshitomi, S ;
Tanaka, T ;
Sato, H ;
Arii, S ;
Seiki, M ;
Imamura, M .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1998, 124 (02) :65-72