Why Integrin as a Primary Target for Imaging and Therapy

被引:161
作者
Niu, Gang [1 ,2 ]
Chen, Xiaoyuan [1 ]
机构
[1] NIBIB, LOMIN, NIH, Bethesda, MD 20892 USA
[2] NIH, Imaging Sci Training Program, Ctr Clin, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
Integrin; inside-out signaling; outside-in signaling; cell adhesion molecule; angiogenesis; ENDOTHELIAL GROWTH-FACTOR; COLON-CARCINOMA CELLS; ALPHA-V-BETA-6; INTEGRIN; STRUCTURAL BASIS; CYTOPLASMIC DOMAIN; TUMOR-GROWTH; IN-VIVO; EXTRACELLULAR-MATRIX; MONOCLONAL-ANTIBODY; CRYSTAL-STRUCTURE;
D O I
10.7150/thno/v01p0030
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Integrin-mediated cell adhesion is involved in many essential normal cellular and pathological functions including cell survival, growth, differentiation, migration, inflammatory responses, platelet aggregation, tissue repair and tumor invasion. 24 different heterodimerized transmembrane integrin receptors are combined from 18 different alpha and 8 different beta subunits. Each integrin subunit contains a large extracellular domain, a single transmembrane domain and a usually short cytoplasmic domain. Integrins bind extracellular matrix (ECM) proteins through their large extracellular domain, and engage the cytoskeleton via their short cytoplasmic tails. These integrin-mediated linkages on either side of the plasma membrane are dynamically linked. Thus, integrins communicate over the plasma membrane in both directions, i.e., outside-in and inside-out signaling. In outside-in signaling through integrins, conformational changes of integrin induced by ligand binding on the extracellular domain altered the cytoplasmic domain structures to elicit various intracellular signaling pathways. Inside-out signaling originates from non-integrin cell surface receptors or cytoplasmic molecules and it activates signaling pathways inside the cells, ultimately resulting in the activation/deactivation of integrins. Integrins are one of key family proteins for cell adhesion regulation through binding to a large number of ECM molecules and cell membrane proteins. Lack of expression of integrins may result in a wide variety of effects ranging from blockage in pre-implantation to embryonic or perinatal lethality and developmental defects. Based on both the key role they played in angiogenesis, leukocytes function and tumor development and easy accessibility as cell surface receptors interacting with extracellular ligands, the integrin superfamily represents the best opportunity of targeting both antibodies and small-molecule antagonists for both therapeutic and diagnostic utility in various key diseases so far.
引用
收藏
页码:30 / 47
页数:18
相关论文
共 187 条
[1]   THE ALPHA-V-BETA-6 INTEGRIN PROMOTES PROLIFERATION OF COLON-CARCINOMA CELLS THROUGH A UNIQUE REGION OF THE BETA-6 CYTOPLASMIC DOMAIN [J].
AGREZ, M ;
CHEN, A ;
CONE, RI ;
PYTELA, R ;
SHEPPARD, D .
JOURNAL OF CELL BIOLOGY, 1994, 127 (02) :547-556
[2]   αvβ6 integrin-A marker for the malignant potential of epithelial ovarian cancer [J].
Ahmed, N ;
Riley, C ;
Rice, GE ;
Quinn, MA ;
Baker, MS .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2002, 50 (10) :1371-1379
[3]   Overexpression of αvβ6 integrin in serous epithelial ovarian cancer regulates extracellular matrix degradation via the plasminogen activation cascade [J].
Ahmed, N ;
Pansino, F ;
Clyde, R ;
Murthi, P ;
Quinn, MA ;
Rice, GE ;
Agrez, MV ;
Mok, S ;
Baker, MS .
CARCINOGENESIS, 2002, 23 (02) :237-244
[4]   From rolling to arrest on blood vessels: leukocyte tap dancing on endothelial integrin ligands and chemokines at sub-second contacts [J].
Alon, R ;
Feigelson, S .
SEMINARS IN IMMUNOLOGY, 2002, 14 (02) :93-104
[5]   Force as a facilitator of integrin conformational changes during leukocyte arrest on blood vessels and antigen-presenting cells [J].
Alon, Ronen ;
Dustin, Michael L. .
IMMUNITY, 2007, 26 (01) :17-27
[6]   VASCULAR ENDOTHELIAL GROWTH-FACTOR ACTS AS A SURVIVAL FACTOR FOR NEWLY FORMED RETINAL-VESSELS AND HAS IMPLICATIONS FOR RETINOPATHY OF PREMATURITY [J].
ALON, T ;
HEMO, I ;
ITIN, A ;
PEER, J ;
STONE, J ;
KESHET, E .
NATURE MEDICINE, 1995, 1 (10) :1024-1028
[7]  
ANDERSON DC, 1987, ANNU REV MED, V38, P175, DOI 10.1146/annurev.med.38.1.175
[8]   Src kinase activation by direct interaction with the integrin β cytoplasmic domain [J].
Arias-Salgado, EG ;
Lizano, S ;
Sarkar, S ;
Brugge, JS ;
Ginsberg, MH ;
Shattil, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (23) :13298-13302
[9]   Significance of α9β31 and αvβ 6 integrin expression in breast carcinoma [J].
Arihiro K. ;
Kaneko M. ;
Fujii S. ;
Inai K. ;
Yokosaki Y. .
Breast Cancer, 2000, 7 (1) :19-26
[10]   Integrin structure, allostery, and bidirectional signaling [J].
Arnaout, MA ;
Mahalingam, B ;
Xiong, JP .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2005, 21 :381-410