Wnt signaling in development, disease and translational medicine

被引:58
作者
Coombs, Gary S. [1 ]
Covey, Tracy M. [1 ]
Virshup, David M. [1 ]
机构
[1] Duke NUS Grad Med Sch, Program Canc & Stem Cell Biol, Singapore 169547, Singapore
关键词
D O I
10.2174/138945008784911796
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Wnt signaling regulates a multitude of critical processes in development and tissue homeostasis. The wingless (wg) gene product was first identified in Drosophila in 1973. Subsequently, the proto-oncogene INT-1 was identified in mice in 1984 when its activation by mouse mammary tumor virus' proviral insertion was found to induce tumor formation. The discovery in 1987 that wg and INT-1 are orthologues contributed to an appreciation of the intimate connection between oncogenic and developmental processes. Diverse diseases including cancer, diabetes, osteoporosis and psychiatric disorders may be amenable to treatment via modulation of Wnt-mediated signaling pathways. There are a number of attractive targets that are the object of ongoing drug development studies aiming to capitalize on these opportunities. In this review, we present a historical overview of key events in this field that have elucidated the known signaling cascades associated with Wnt ligands and shaped our understanding of the roles of these cascades in physiological and pathological processes.
引用
收藏
页码:513 / 531
页数:19
相关论文
共 205 条
[91]   Wnt/β-catenin -: A canonical tale of cell-fate choice in the vertebrate skeleton [J].
Kolpakova, E ;
Olsen, BR .
DEVELOPMENTAL CELL, 2005, 8 (05) :626-627
[92]   Constitutive transcriptional activation by a beta-catenin-Tcf complex in APC(-/-) colon carcinoma [J].
Korinek, V ;
Barker, N ;
Morin, PJ ;
vanWichen, D ;
deWeger, R ;
Kinzler, KW ;
Vogelstein, B ;
Clevers, H .
SCIENCE, 1997, 275 (5307) :1784-1787
[93]  
Kühl M, 2000, TRENDS GENET, V16, P279, DOI 10.1016/s0168-9525(00)02028-x
[94]   Essential requirement for Wnt signaling in proliferation of adult small intestine and colon revealed by adenoviral expression of Dickkopf-1 [J].
Kuhnert, F ;
Davis, CR ;
Wang, HT ;
Chu, P ;
Lee, M ;
Yuan, J ;
Nusse, R ;
Kuo, CJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (01) :266-271
[95]   The type of somatic mutation at APC in familial adenomatous polyposis is determined by the site of the germline mutation:: a new facet to Knudson's 'two-hit' hypothesis [J].
Lamlum, H ;
Ilyas, M ;
Rowan, A ;
Clark, S ;
Johnson, V ;
Bell, J ;
Frayling, I ;
Efstathiou, J ;
Pack, K ;
Payne, S ;
Roylance, R ;
Gorman, P ;
Sheer, D ;
Neale, K ;
Phillips, R ;
Talbot, I ;
Bodmer, W ;
Tomlinson, I .
NATURE MEDICINE, 1999, 5 (09) :1071-1075
[96]   Small-molecule antagonists of the oncogenic Tcf/β-catenin protein complex [J].
Lepourcelet, M ;
Chen, YNP ;
France, DS ;
Wang, HS ;
Crews, P ;
Petersen, F ;
Bruseo, C ;
Wood, AW ;
Shivdasani, RA .
CANCER CELL, 2004, 5 (01) :91-102
[97]   Sclerostin binds to LRP5/6 and antagonizes canonical Wnt signaling [J].
Li, XF ;
Zhang, YZ ;
Kang, HS ;
Liu, WZ ;
Liu, P ;
Zhang, JG ;
Harris, SE ;
Wu, DQ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (20) :19883-19887
[98]   Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1 [J].
Lijam, N ;
Paylor, R ;
McDonald, MP ;
Crawley, JN ;
Deng, CX ;
Herrup, K ;
Stevens, KE ;
Maccaferri, G ;
McBain, CJ ;
Sussman, DJ ;
WynshawBoris, A .
CELL, 1997, 90 (05) :895-905
[99]   A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait [J].
Little, RD ;
Carulli, JP ;
Del Mastro, RG ;
Dupuis, J ;
Osborne, M ;
Folz, C ;
Manning, SP ;
Swain, PM ;
Zhao, SC ;
Eustace, B ;
Lappe, MM ;
Spitzer, L ;
Zweier, S ;
Braunschweiger, K ;
Benchekroun, Y ;
Hu, XT ;
Adair, R ;
Chee, L ;
FitzGerald, MG ;
Tulig, C ;
Caruso, A ;
Tzellas, N ;
Bawa, A ;
Franklin, B ;
McGuire, S ;
Nogues, X ;
Gong, G ;
Allen, KM ;
Anisowicz, A ;
Morales, AJ ;
Lomedico, PT ;
Recker, SM ;
Van Eerdewegh, P ;
Recker, RR ;
Johnson, ML .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (01) :11-19
[100]   Control of β-catenin phosphorylation/degradation by a dual-kinase mechanism [J].
Liu, CM ;
Li, YM ;
Semenov, M ;
Han, C ;
Baeg, GH ;
Tan, Y ;
Zhang, ZH ;
Lin, XH ;
He, X .
CELL, 2002, 108 (06) :837-847