Osteopontin: regulation in tumor metastasis

被引:417
作者
Wai, Philip Y. [1 ]
Kuo, Paul C. [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Surg, Durham, NC 27710 USA
关键词
cancer; metastasis; osteopontin; integrin; matrix-metalloproteinase;
D O I
10.1007/s10555-007-9104-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Osteopontin is a secreted phosphoprotein that has been implicated as an important mediator of tumor metastasis and has been investigated for use as a biomarker for advanced disease and as a potential therapeutic target in the regulation of cancer metastasis. The OPN DNA sequence is highly conserved and the protein contains several important functional domains including alpha(v)beta integrin and CD44 binding sites. High levels of OPN expression correlate with tumor invasion, progression or metastasis in multiple cancer. Studies demonstrate that osteopontin mediates the molecular mechanisms which determine metastatic spread, such as prevention of apoptosis, extracellular matrix proteolysis and remodeling, cell migration, evasion of host-immune cells and neovascularization. Transcriptional regulation of OPN is complex and involves multiple pathways, including AP-1, Myc, v-Src, Runx/CBF, TGF-B/BMPs/Smad/Hox, and Wnt/beta-cocatenin/APC/GSK-3 beta/Tcf-4. The current state of knowledge of OPN biology suggests that it is an attractive target for therapeutic modulation of metastatic disease.
引用
收藏
页码:103 / 118
页数:16
相关论文
共 233 条
[1]
Downregulation of osteopontin and bone sialoprotein II is related to reduced colony formation and metastasis formation of MDA-MB-231 human breast cancer cells [J].
Adwan, H ;
Bäuerle, TJ ;
Berger, MR .
CANCER GENE THERAPY, 2004, 11 (02) :109-120
[2]
Agrawal D, 2002, J NATL CANCER I, V94, P513
[3]
Andreasen PA, 1997, INT J CANCER, V72, P1, DOI 10.1002/(SICI)1097-0215(19970703)72:1<1::AID-IJC1>3.0.CO
[4]
2-Z
[5]
Osteopontin modulates prostate carcinoma invasive capacity through RGD-dependent upregulation of plasminogen activators [J].
Angelucci, A ;
Festuccia, C ;
D'Andrea, G ;
Teti, A ;
Bologna, M .
BIOLOGICAL CHEMISTRY, 2002, 383 (01) :229-234
[6]
REGULATION OF THE JUNB GENE BY V-SRC [J].
APEL, I ;
YU, CL ;
WANG, T ;
DOBRY, C ;
VANANTWERP, ME ;
JOVE, R ;
PROCHOWNIK, EV .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (08) :3356-3364
[7]
Cancer treatment by targeted drug delivery to tumor vasculature in a mouse model [J].
Arap, W ;
Pasqualini, R ;
Ruoslahti, E .
SCIENCE, 1998, 279 (5349) :377-380
[8]
Identification and characterization of high glucose and glucosamine responsive element in the rat osteopontin promoter [J].
Asaumi, S ;
Takemoto, M ;
Yokote, K ;
Ridall, AL ;
Butler, WT ;
Fujimoto, M ;
Kobayashi, K ;
Kawamura, H ;
Take, A ;
Saito, Y ;
Mori, S .
JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2003, 17 (01) :34-38
[9]
Eta-1 (osteopontin): An early component of type-1 (cell-mediated) immunity [J].
Ashkar, S ;
Weber, GF ;
Panoutsakopoulou, V ;
Sanchirico, ME ;
Jansson, M ;
Zawaideh, S ;
Rittling, SR ;
Denhardt, DT ;
Glimcher, MJ ;
Cantor, H .
SCIENCE, 2000, 287 (5454) :860-864
[10]
Asosingh K, 2000, CANCER RES, V60, P3096