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骨形态发生蛋白信号通路在唇腭裂发育中的作用。

Roles of BMP signaling pathway in lip and palate development.

作者信息

Parada Carolina, Chai Yang

机构信息

Center for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA, USA.

出版信息

Front Oral Biol. 2012;16:60-70. doi: 10.1159/000337617. Epub 2012 Jun 25.


DOI:10.1159/000337617
PMID:22759670
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3661199/
Abstract

Cleft lip with or without cleft palate (CLP) and cleft palate only (CP) are severe disruptions affecting orofacial structures. Patients with orofacial clefts require complex interdisciplinary care, which includes nursing, plastic surgery, maxillofacial surgery, otolaryngology, speech therapy, audiology, psychological and genetic counseling, orthodontics and dental treatment, among others. Overall, treatment of clefts of the lip and palate entails a significant economic burden for families and society. Therefore, prevention is the ultimate objective and this will be facilitated by a complete understanding of the etiology of this condition. Here we review the current concepts regarding the genetic and environmental factors contributing to orofacial clefts and emphasize on the roles of BMP signaling pathway components in the normal and aberrant development of the lip and palate.

摘要

唇裂伴或不伴腭裂(CLP)以及仅腭裂(CP)是影响口面部结构的严重畸形。患有口面部裂的患者需要复杂的多学科护理,其中包括护理、整形手术、颌面外科、耳鼻喉科、言语治疗、听力学、心理和遗传咨询、正畸和牙科治疗等。总体而言,唇腭裂的治疗给家庭和社会带来了巨大的经济负担。因此,预防是最终目标,而全面了解这种疾病的病因将有助于实现这一目标。在这里,我们回顾了关于导致口面部裂的遗传和环境因素的当前概念,并强调了骨形态发生蛋白(BMP)信号通路成分在唇腭裂正常和异常发育中的作用。

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[1]
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引用本文的文献

[1]
Molecular Regulation of Palatogenesis and Clefting: An Integrative Analysis of Genetic, Epigenetic Networks, and Environmental Interactions.

Int J Mol Sci. 2025-2-6

[2]
Protective effect of extract against all-trans-retinoic acid-induced inhibition of proliferation of cultured human palate cells.

Nagoya J Med Sci. 2024-5

[3]
Characteristics of Factors Influencing the Occurrence of Cleft Lip and/or Palate: A Case Analysis and Literature Review.

Children (Basel). 2024-3-28

[4]
Grainyhead-like 2 interacts with noggin to regulate tissue fusion in mouse.

Development. 2024-3-1

[5]
Orofacial Clefts: Genetics of Cleft Lip and Palate.

Genes (Basel). 2023-8-9

[6]
Modifiable Risk Factors of Non-Syndromic Orofacial Clefts: A Systematic Review.

Children (Basel). 2022-11-28

[7]
Single-cell transcriptomic signatures and gene regulatory networks modulated by Wls in mammalian midline facial formation and clefts.

Development. 2022-7-15

[8]
Condylar Changes after Maxillary Expansion in Children with Cleft Lip and Palate-A Three-Dimensional Retrospective Study.

Biomimetics (Basel). 2022-6-5

[9]
Revisiting the embryogenesis of lip and palate development.

Oral Dis. 2022-7

[10]
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Elife. 2022-2-25

本文引用的文献

[1]
Association of MSX1 799 G>T variant with nonsyndromic cleft lip/palate in South Indian adolescent patients.

Int J Paediatr Dent. 2011-10-4

[2]
Contribution of MSX1 variants to the risk of non-syndromic cleft lip and palate in a Malay population.

J Hum Genet. 2011-8-25

[3]
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DNA Cell Biol. 2011-6-20

[4]
The mechanism of TGF-β signaling during palate development.

Oral Dis. 2011-3-13

[5]
Cleft lip and palate: understanding genetic and environmental influences.

Nat Rev Genet. 2011-3

[6]
Bmpr1a signaling plays critical roles in palatal shelf growth and palatal bone formation.

Dev Biol. 2010-12-23

[7]
Maternal alcohol consumption, alcohol metabolism genes, and the risk of oral clefts: a population-based case-control study in Norway, 1996-2001.

Am J Epidemiol. 2010-9-1

[8]
Modulation of BMP signaling by Noggin is required for the maintenance of palatal epithelial integrity during palatogenesis.

Dev Biol. 2010-8-19

[9]
MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate.

Eur J Oral Sci. 2010-6

[10]
Bone morphogenetic protein 7 (BMP7) mutations are associated with variable ocular, brain, ear, palate, and skeletal anomalies.

Hum Mutat. 2010-7

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