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导致缺牙症的基因网络。

The Gene Network Underlying Hypodontia.

机构信息

The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) & Key Laboratory of Oral Biomedicine Ministry of Education, School & Hospital of Stomatology, Wuhan University, Wuhan, China State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, China Department of Endodontics & Periodontics, College of Stomatology, Dalian Medical University, Dalian, China.

The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) & Key Laboratory of Oral Biomedicine Ministry of Education, School & Hospital of Stomatology, Wuhan University, Wuhan, China

出版信息

J Dent Res. 2015 Jul;94(7):878-85. doi: 10.1177/0022034515583999. Epub 2015 Apr 24.


DOI:10.1177/0022034515583999
PMID:25910507
Abstract

Mammalian tooth development is a precise and complicated procedure. Several signaling pathways, such as nuclear factor (NF)-κB and WNT, are key regulators of tooth development. Any disturbance of these signaling pathways can potentially affect or block normal tooth development, and presently, there are more than 150 syndromes and 80 genes known to be related to tooth agenesis. Clarifying the interaction and crosstalk among these genes will provide important information regarding the mechanisms underlying missing teeth. In the current review, we summarize recently published findings on genes related to isolated and syndromic tooth agenesis; most of these genes function as positive regulators of cell proliferation or negative regulators of cell differentiation and apoptosis. Furthermore, we explore the corresponding networks involving these genes in addition to their implications for the clinical management of tooth agenesis. We conclude that this requires further study to improve patients' quality of life in the future.

摘要

哺乳动物牙齿发育是一个精确而复杂的过程。几种信号通路,如核因子 (NF)-κB 和 WNT,是牙齿发育的关键调节剂。这些信号通路的任何干扰都可能影响或阻断正常的牙齿发育,目前已知有超过 150 种综合征和 80 个与牙齿缺失相关的基因。阐明这些基因之间的相互作用和串扰将为缺失牙齿的机制提供重要信息。在本综述中,我们总结了最近关于与孤立性和综合征性牙齿缺失相关基因的研究发现;这些基因中的大多数作为细胞增殖的正调节剂或细胞分化和凋亡的负调节剂发挥作用。此外,我们还探讨了这些基因涉及的相应网络,以及它们对牙齿缺失临床管理的意义。我们的结论是,这需要进一步的研究,以提高患者的生活质量。

相似文献

[1]
The Gene Network Underlying Hypodontia.

J Dent Res. 2015-4-24

[2]
Dental agenesis: genetic and clinical perspectives.

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[3]
Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis.

Eur J Med Genet. 2008

[4]
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Orthod Craniofac Res. 2007-8

[5]
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[6]
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[7]
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[8]
Genes affecting tooth morphogenesis.

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[9]
[Correlation between the phenotype and genotype of tooth agenesis patients by tooth agenesis code].

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2010-6

[10]
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引用本文的文献

[1]
Genetic Aspects of Tooth Agenesis.

Genes (Basel). 2025-5-15

[2]
A Novel Homozygous Missense Variant with Protein Modeling in a Patient Diagnosed as Short Stature, Facial Dysmorphism, and Skeletal Anomalies with or without Cardiac Anomalies 2.

Mol Syndromol. 2025-3-28

[3]
The fundamentals of WNT10A.

Differentiation. 2025

[4]
Dental Implant Rehabilitation in Patients Carrying WNT10A Mutations With Different Molecular Statuses and Phenotypes: A Retrospective Cohort Study.

Clin Oral Implants Res. 2025-4

[5]
Variants Are Responsible for Approximately 90% of Deciduous Tooth Agenesis.

Int J Mol Sci. 2024-9-27

[6]
Small RNAs and tooth development: The role of microRNAs in tooth agenesis and impaction.

J Dent Sci. 2024-10

[7]
Genotypic and phenotypic correlations in tooth agenesis: insights from WNT10A and EDA mutations in syndromic and non-syndromic forms.

Hum Genet. 2024-11

[8]
Evaluation of mandibular trabecular bone by fractal analysis in pediatric patients with hypodontia of the mandibular second premolar tooth.

BMC Oral Health. 2024-8-27

[9]
What could be the role of genetic tests and machine learning of AXIN2 variant dominance in non-syndromic hypodontia? A case-control study in orthodontically treated patients.

Prog Orthod. 2024-8-26

[10]
Non-syndromic familial congenital dental deficiency: two cases report.

Hua Xi Kou Qiang Yi Xue Za Zhi. 2022-7-25

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