The implications of supernumerary teeth to understand the developmental mechanisms underlying tooth formation
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초록
Dental anomalies are diverse. The most common clinical anomaly interfering with the tooth numbering system is supernumerary teeth (ST). Teeth are created by the reciprocal interactions of the surface epithelium ectoderm and the neural crest-derived mesenchyme regulated by numerous signaling molecules including SHH, WNT, BMP, FGF, and Eda. Any alteration or disruption to these signaling molecules may lead to severe tooth malformations. Various mice models have been used to investigate the related etiology and potential candidate genes involved in the pathogenesis of ST. ST can occur as sporadic conditions but are mostly associated with genetic syndromes. An understanding of the molecular basis of ST and the associated syndromes may help clinicians in early diagnosis and constructive treatment planning. The findings of this literature review on ST contribute to further understanding of tooth development and regeneration.
Abstract
Dental anomalies are diverse. The most common clinical anomaly interfering with the tooth numbering system is supernumerary teeth (ST). Teeth are created by the reciprocal interactions of the surface epithelium ectoderm and the neural crest-derived mesenchyme regulated by numerous signaling molecules including SHH, WNT, BMP, FGF, and Eda. Any alteration or disruption to these signaling molecules may lead to severe tooth malformations. Various mice models have been used to investigate the related etiology and potential candidate genes involved in the pathogenesis of ST. ST can occur as sporadic conditions but are mostly associated with genetic syndromes. An understanding of the molecular basis of ST and the associated syndromes may help clinicians in early diagnosis and constructive treatment planning. The findings of this literature review on ST contribute to further understanding of tooth development and regeneration.
참고문헌 (84)
- Tingsheng Yu, "Molecular and cellular mechanisms of tooth development, homeostasis and repair", Development, 147(2) (2020), The Company of Biologists[DOI]
- Hyejin Seo, "Regulation of root patterns in mammalian teeth", Scientific Reports, 7(1) (2017), Springer Science and Business Media LLC[DOI]
- Javier Catón, "Current knowledge of tooth development: patterning and mineralization of the murine dentition", Journal of Anatomy, 214(4), pp.502~515 (2009), Wiley[DOI]
- Muriel de La Dure‐Molla, "Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders", American Journal of Medical Genetics Part A, 179(10), pp.1913~1981 (2019), Wiley[DOI]
- Nareh Eshgian, "Prevalence of hyperdontia, hypodontia, and concomitant hypo-hyperdontia", Journal of Dental Sciences, 16(2), pp.713~717 (2021), Elsevier BV[DOI]
- R. P. Anthonappa, "Aetiology of supernumerary teeth: a literature review", European Archives of Paediatric Dentistry, 14(5), pp.279~288 (2013), Springer Science and Business Media LLC[DOI]
- Dalia M. Talaat, "Assessment of risk factors and molecular biomarkers in children with supernumerary teeth: a single-center study", BMC Oral Health, 22(1) (2022), Springer Science and Business Media LLC[DOI]
- MustafaCenk Durmuslar, "Prevalence and characteristics of supernumerary teeth: A survey on 7348 people", Journal of International Society of Preventive and Community Dentistry, 5(7), pp.39~ (2015), Medknow[DOI]
- S. Tetay-Salgado, "Prevalence of impacted teeth and supernumerary teeth by radiographic evaluation in three Latin American countries: A cross-sectional study", Journal of Clinical and Experimental Dentistry, pp.e363~e368 (2021), Medicina Oral, S.L.[DOI]
- Sreekanth Kumar Mallineni, "Supernumerary Teeth: Review of the Literature with Recent Updates", Conference Papers in Science, 2014, pp.1~6 (2014), Hindawi Limited[DOI]
- Si-Yeon Park, "Complications associated with specific characteristics of supernumerary teeth", Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology, 130(2), pp.150~155 (2020), Elsevier BV[DOI]
- E. Juuri, "The Biology Underlying Abnormalities of Tooth Number in Humans", Journal of Dental Research, 96(11), pp.1248~1256 (2017), SAGE Publications[DOI]
- Tangade P, "Non-syndromic unilateral supplemental maxillary central incisor : a case report", Ethiop J Health Sci, 23(3), pp.289~292 (2013)
- Aslı Subasioglu, "Genetic background of supernumerary teeth", European Journal of Dentistry, 09(01), pp.153~158 (2015), Georg Thieme Verlag KG[DOI]
- undefined, "Main genetic entities associated with supernumerary teeth", Archivos Argentinos de Pediatria, 116(6) (2018), Sociedad Argentina de Pediatria[DOI]
- Mark Lubinsky, "Syndromes with supernumerary teeth", American Journal of Medical Genetics Part A, 170(10), pp.2611~2616 (2016), Wiley[DOI]
- Masahiro Takahashi, "Whole-exome sequencing analysis of supernumerary teeth occurrence in Japanese individuals", Human Genome Variation, 4(1) (2017), Springer Science and Business Media LLC[DOI]
- Ewa Hordyjewska, "Novel Mutation of the RUNX2 Gene in Patients with Cleidocranial Dysplasia", Molecular Syndromology, 8(5), pp.253~260 (2017), S. Karger AG[DOI]
- Fang Yu, "A novel mutation of adenomatous polyposis coli (APC) gene results in the formation of supernumerary teeth", Journal of Cellular and Molecular Medicine, 22(1), pp.152~162 (2017), Wiley[DOI]
- Yeliz Guven, "Nance-Horan Syndrome: characterization of dental, clinical and molecular features in three new families", BMC Oral Health, 23(1) (2023), Springer Science and Business Media LLC[DOI]
- Hans Gjørup, "Nance–Horan syndrome—The oral perspective on a rare disease", American Journal of Medical Genetics Part A, 173(1), pp.88~98 (2016), Wiley[DOI]
- Parastoo Momeni, "Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I", Nature Genetics, 24(1), pp.71~74 (2000), Springer Science and Business Media LLC[DOI]
- Cedrik Tekendo‐Ngongang, "Rubinstein-Taybi syndrome in diverse populations", American Journal of Medical Genetics Part A, 182(12), pp.2939~2950 (2020), Wiley[DOI]
- Chikahiko Numakura, "Supernumerary impacted teeth in a patient with <i>SOX2<", i> anophthalmia syndrome, 2010, pp.152A(9), 2355~2359[DOI]
- Oscar Francisco Chacon‐Camacho, "SOX2 anophthalmia syndrome and dental anomalies", American Journal of Medical Genetics Part A, 167(11), pp.2830~2833 (2015), Wiley[DOI]
- S. Hosseini-Farahabadi, "Abnormal WNT5A Signaling Causes Mandibular Hypoplasia in Robinow Syndrome", Journal of Dental Research, 96(11), pp.1265~1272 (2017), SAGE Publications[DOI]
- Christopher J. Conlon, "Craniofacial phenotypes associated with <scp>Robinow<", scp> syndrome, 2020, pp.185(12), 3606~3612[DOI]
- da Fonseca M, "Hallerman-Streiff syndrome : case report and recommendations for dental care", ASDDC Journal of dentistry for children, 61, pp.2~ (1994)
- Maria I. Ferrante, "Identification of the Gene for Oral-Facial-Digital Type I Syndrome", The American Journal of Human Genetics, 68(3), pp.569~576 (2001), Elsevier BV[DOI]
- Tomoyo Yamashita, "Oculofaciocardiodental syndrome caused by a novel BCOR variant", Human Genome Variation, 10(1) (2023), Springer Science and Business Media LLC[DOI]
- Elizabeth Half, "Familial adenomatous polyposis", Orphanet Journal of Rare Diseases, 4(1) (2009), Springer Science and Business Media LLC[DOI]
- Sapna Panjwani, "Gardner's Syndrome", Journal of Clinical Imaging Science, 1, pp.65~ (2011), Scientific Scholar[DOI]
- Nadav Shoshany, "NHS Gene Mutations in Ashkenazi Jewish Families with Nance-Horan Syndrome", Current Eye Research, 42(9), pp.1240~1244 (2017), Informa UK Limited[DOI]
- Shambhu Sharma, "Nance–Horan syndrome: A rare case report", Contemporary Clinical Dentistry, 8(3), pp.469~ (2017), Medknow[DOI]
- Renaud Preudhomme, "Hallermann Streiff syndrome: Cranio-facial manifestations systematic review and report of two cases", Journal of Stomatology, Oral and Maxillofacial Surgery, 123(4), pp.e219~e223 (2022), Elsevier BV[DOI]
- Martyn T. Cobourne, "Making up the numbers: The molecular control of mammalian dental formula", Seminars in Cell & Developmental Biology, 21(3), pp.314~324 (2010), Elsevier BV[DOI]
- Georgia Palikaraki, "Two Rare Cases of Non-Syndromic Paramolars with Family Occurrence and a Review of Literature", Dentistry Journal, 7(2), pp.38~ (2019), MDPI AG[DOI]
- J.S. Shim, "Temporal Control of WNT Activity Regulates Tooth Number in Fish", Journal of Dental Research, 98(3), pp.339~346 (2018), SAGE Publications[DOI]
- Suhailiza S, "Genetic basis of supernumerary tooth", Journal of Biomedical and Clinical Sciences, 4(1) (2019)
- Rebecca Kim, "Early perturbation of Wnt signaling reveals patterning and invagination-evagination control points in molar tooth development", Development, 148(14) (2021), The Company of Biologists[DOI]
- Fei Liu, "Wnt", β-catenin signaling directs multiple stages of tooth morphogenesis, 2008, pp.313(1), 210~224[DOI]
- Nobue Itasaki, "Wise, a context-dependent activator and inhibitor of Wnt signalling", Development, 130(18), pp.4295~4305 (2003), The Company of Biologists[DOI]
- Akiko Murashima-Suginami, "Enhanced BMP signaling results in supernumerary tooth formation in USAG-1 deficient mouse", Biochemical and Biophysical Research Communications, 369(4), pp.1012~1016 (2008), Elsevier BV[DOI]
- Atsushi Ohazama, "Lrp4 Modulates Extracellular Integration of Cell Signaling Pathways in Development", PLoS ONE, 3(12), pp.e4092~ (2008), Public Library of Science (PLoS)[DOI]
- Marianna Bei, "Molecular genetics of tooth development", Current Opinion in Genetics & Development, 19(5), pp.504~510 (2009), Elsevier BV[DOI]
- J. Blackburn, "Excess NF-κB Induces Ectopic Odontogenesis in Embryonic Incisor Epithelium", Journal of Dental Research, 94(1), pp.121~128 (2014), SAGE Publications[DOI]
- Jo-Maree Courtney, "The Ectodysplasin and NFκB signalling pathways in odontogenesis", Archives of Oral Biology, 50(2), pp.159~163 (2005), Elsevier BV[DOI]
- Xi Lu, "Advances of Wnt signalling pathway in dental development and potential clinical application", Organogenesis, 15(4), pp.101~110 (2019), Informa UK Limited[DOI]
- Maiko kawasaki, "R‐spondins", Lgrs expression in tooth development, 2014, pp.243(6), 844~851[DOI]
- Mingang Xu, "WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation", Nature Communications, 8(1) (2017), Springer Science and Business Media LLC[DOI]
- Jie Yang, "Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds", Molecular Genetics & Genomic Medicine, 3(1), pp.40~58 (2014), Wiley[DOI]
- Miao Yu, "BMP4 mutations in tooth agenesis and low bone mass", Archives of Oral Biology, 103, pp.40~46 (2019), Elsevier BV[DOI]
- P. S. Fleming, "Revisiting the supernumerary: the epidemiological and molecular basis of extra teeth", British Dental Journal, 208(1), pp.25~30 (2010), Springer Science and Business Media LLC[DOI]
- J.-M. Lee, "MSX1 Drives Tooth Morphogenesis Through Controlling Wnt Signaling Activity", Journal of Dental Research, 101(7), pp.832~839 (2022), SAGE Publications[DOI]
- Zunyi Zhang, "Antagonistic Actions of Msx1 and Osr2 Pattern Mammalian Teeth into a Single Row", Science, 323(5918), pp.1232~1234 (2009), American Association for the Advancement of Science (AAAS)[DOI]
- Shihai Jia, "Bmp4-Msx1 signaling and Osr2 control tooth organogenesis through antagonistic regulation of secreted Wnt antagonists", Developmental Biology, 420(1), pp.110~119 (2016), Elsevier BV[DOI]
- Lu Zheng, "Sonic hedgehog signaling in epithelial tissue development", Regenerative Medicine Research, 7, pp.3~ (2019), EDP Sciences[DOI]
- H. Seo, "Upstream Enhancer Elements of<i>Shh<", i>Regulate Oral and Dental Patterning, 2018, pp.97(9), 1055~1063[DOI]
- Tomoko Sagai, "SHH signaling directed by two oral epithelium-specific enhancers controls tooth and oral development", Scientific Reports, 7(1) (2017), Springer Science and Business Media LLC[DOI]
- M. Seppala, "Gas1 Regulates Patterning of the Murine and Human Dentitions through Sonic Hedgehog", Journal of Dental Research, 101(4), pp.473~482 (2021), SAGE Publications[DOI]
- Atsushi Ohazama, "Primary cilia regulate Shh activity in the control of molar tooth number", Development, 136(6), pp.897~903 (2009), The Company of Biologists[DOI]
- Pauline Marangoni, "Downregulation of FGF Signaling by Spry4 Overexpression Leads to Shape Impairment, Enamel Irregularities, and Delayed Signaling Center Formation in the Mouse Molar", JBMR Plus, 3(8) (2019), Oxford University Press (OUP)[DOI]
- Wen Du, "The Role of Fibroblast Growth Factors in Tooth Development and Incisor Renewal", Stem Cells International, 2018, pp.1~14 (2018), Hindawi Limited[DOI]
- Y. Chen, "Activated Epithelial FGF8 Signaling Induces Fused Supernumerary Incisors", Journal of Dental Research, 101(4), pp.458~464 (2021), SAGE Publications[DOI]
- Lu Li, "Exogenous fibroblast growth factor 8 rescues development of mouse diastemal vestigial tooth ex vivo", Developmental Dynamics, 240(6), pp.1344~1353 (2011), Wiley[DOI]
- Balic A, "Current Topics in Developmental Biology. 115", pp.157~186 (2015), Academic Press
- Ophir D. Klein, "Sprouty Genes Control Diastema Tooth Development via Bidirectional Antagonism of Epithelial-Mesenchymal FGF Signaling", Developmental Cell, 11(2), pp.181~190 (2006), Elsevier BV[DOI]
- Cyril Charles, "Regulation of tooth number by fine-tuning levels of receptor-tyrosine kinase signaling", Development, 138(18), pp.4063~4073 (2011), The Company of Biologists[DOI]
- Takashi Nakamura, "Transcription Factor Epiprofin Is Essential for Tooth Morphogenesis by Regulating Epithelial Cell Fate and Tooth Number", Journal of Biological Chemistry, 283(8), pp.4825~4833 (2008), Elsevier BV[DOI]
- Sung-Won Cho, "Interactions between Shh, Sostdc1 and Wnt signaling and a new feedback loop for spatial patterning of the teeth", Development, 138(9), pp.1807~1816 (2011), The Company of Biologists[DOI]
- Jingyi Wu, "FAM20B-catalyzed glycosaminoglycans control murine tooth number by restricting FGFR2b signaling", BMC Biology, 18(1) (2020), Springer Science and Business Media LLC[DOI]
- Kazuyuki Saito, "Loss of Stemness, EMT, and Supernumerary Tooth Formation in Cebpb−", −Runx2+, Scientific Reports, pp.2018, 8(1)[DOI]
- Kaufman MH, "Craniofacial abnormalities in homozygous Small eye(Sey", Sey)embryos and newborn mice, 1995, pp.186(Pt 3), 607~617
- C H Danforth, "THE OCCURRENCE AND GENETIC BEHAVIOR OF DUPLICATE LOWER INCISORS IN THE MOUSE", Genetics, 43(1), pp.139~148 (1958), Oxford University Press (OUP)[DOI]
- Youngwook Ahn, "Inhibition of Wnt signaling by Wise (Sostdc1) and negative feedback from Shh controls tooth number and patterning", Development, 137(19), pp.3221~3231 (2010), The Company of Biologists[DOI]
- Renata Peterkova, "Revitalization of a diastemal tooth primordium in <i>Spry2<", i> null mice results from increased proliferation and decreased apoptosis, 2009, pp.312B(4), 292~308[DOI]
- Ophir D. Klein, "Sprouty Genes Control Diastema Tooth Development via Bidirectional Antagonism of Epithelial-Mesenchymal FGF Signaling", Developmental Cell, 11(2), pp.181~190 (2006), Elsevier BV[DOI]
- A.S Tucker, "The activation level of the TNF family receptor, Edar, determines cusp number and tooth number during tooth development", Developmental Biology, 268(1), pp.185~194 (2004), Elsevier BV[DOI]
- Tuija Mustonen, "Stimulation of ectodermal organ development by Ectodysplasin-A1", Developmental Biology, 259(1), pp.123~136 (2003), Elsevier BV[DOI]
- Otso Häärä, "Ectodysplasin regulates activator-inhibitor balance in murine tooth development through Fgf20 signaling", Development, 139(17), pp.3189~3199 (2012), The Company of Biologists[DOI]
- Renata Peterkova, "Phylogenetic memory of developing mammalian dentition", Journal of Experimental Zoology Part B: Molecular and Developmental Evolution, 306B(3), pp.234~250 (2006), Wiley[DOI]
- Cyril Charles, "Distinct Impacts of Eda and Edar Loss of Function on the Mouse Dentition", PLoS ONE, 4(4), pp.e4985~ (2009), Public Library of Science (PLoS)[DOI]
- Virginie Laugel-Haushalter, "RSK2 Is a Modulator of Craniofacial Development", PLoS ONE, 9(1), pp.e84343~ (2014), Public Library of Science (PLoS)[DOI]
- Qihong Zhang, "Loss of the Tg737protein results in skeletal patterning defects", Developmental Dynamics, 227(1), pp.78~90 (2003), Wiley[DOI]
