Molecular Genetics of Supernumerary Tooth Formation

被引:90
作者
Wang, Xiu-Ping [1 ]
Fan, Jiabing [1 ]
机构
[1] Harvard Univ, Sch Dent Med, Dept Dev Biol, Boston, MA 02115 USA
关键词
supernumerary teeth; cleidocranial dysplasia; familiar adenomatous polyposis; Runx2; Apc; tooth development; tooth replacement; successional tooth; FAMILIAL ADENOMATOUS POLYPOSIS; OF-THE-LITERATURE; NANCE-HORAN-SYNDROME; GENOTYPE-PHENOTYPE CORRELATIONS; EHLERS-DANLOS-SYNDROME; EPITHELIAL STEM-CELLS; CLEIDOCRANIAL DYSPLASIA; TRANSCRIPTION FACTOR; GARDNERS-SYNDROME; APC GENE;
D O I
10.1002/dvg.20715
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Despite advances in the knowledge of tooth morphogenesis and differentiation, relatively little is known about the aetiology and molecular mechanisms underlying supernumerary tooth formation. A small number of supernumerary teeth may be a common developmental dental anomaly, while multiple supernumerary teeth usually have a genetic component and they are sometimes thought to represent a partial third dentition in humans. Mice, which are commonly used for studying tooth development, only exhibit one dentition, with very few mouse models exhibiting supernumerary teeth similar to those in humans. Inactivation of Apc or forced activation of Wnt/beta(catenin signalling results in multiple supernumerary tooth formation in both humans and in mice, but the key genes in these pathways are not very clear. Analysis of other model systems with continuous tooth replacement or secondary tooth formation, such as fish, snake, lizard, and ferret, is providing insights into the molecular and cellular mechanisms underlying succesional tooth development, and will assist in the studies on supernumerary tooth formation in humans. This information, together with the advances in stem cell biology and tissue engineering, will pave ways for the tooth regeneration and tooth bioengineering. genesis 49:261-277, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:261 / 277
页数:17
相关论文
共 196 条
[21]  
Brook A H, 1974, J Int Assoc Dent Child, V5, P37
[22]   A UNIFYING ETIOLOGICAL EXPLANATION FOR ANOMALIES OF HUMAN TOOTH NUMBER AND SIZE [J].
BROOK, AH .
ARCHIVES OF ORAL BIOLOGY, 1984, 29 (05) :373-378
[23]  
CADENAT H, 1977, REV STOMATOL CHIR, V78, P341
[24]   FAMILIAL ADENOMATOUS POLYPOSIS - MUTATION AT CODON-1309 AND EARLY-ONSET OF COLON-CANCER [J].
CASPARI, R ;
FRIEDL, W ;
MANDL, M ;
MOSLEIN, G ;
KADMON, M ;
KNAPP, M ;
JACOBASCH, KH ;
ECKER, KW ;
KREISSLERHAAG, D ;
TIMMERMANS, G ;
PROPPING, P .
LANCET, 1994, 343 (8898) :629-632
[25]   FAMILIAL ADENOMATOUS POLYPOSIS - DESMOID TUMORS AND LACK OF OPHTHALMIC LESIONS (CHRPE) ASSOCIATED WITH APC MUTATIONS BEYOND CODON-1444 [J].
CASPARI, R ;
OLSCHWANG, S ;
FRIEDL, W ;
MANDL, M ;
BOISSON, C ;
BOKER, T ;
AUGUSTIN, A ;
KADMON, M ;
MOSLEIN, G ;
THOMAS, G ;
PROPPING, P .
HUMAN MOLECULAR GENETICS, 1995, 4 (03) :337-340
[26]   Distinct Impacts of Eda and Edar Loss of Function on the Mouse Dentition [J].
Charles, Cyril ;
Pantalacci, Sophie ;
Tafforeau, Paul ;
Headon, Denis ;
Laudet, Vincent ;
Viriot, Laurent .
PLOS ONE, 2009, 4 (04)
[27]  
Chen YP, 1996, DEVELOPMENT, V122, P3035
[28]  
Chimenos-Kustner Eduardo, 2005, Med Oral Patol Oral Cir Bucal, V10, P402
[29]   Colon cancer - Understanding how NSAIDs work [J].
Clevers, H .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (07) :761-763
[30]   Making up the numbers: The molecular control of mammalian dental formula [J].
Cobourne, Martyn T. ;
Sharpe, Paul T. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2010, 21 (03) :314-324