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WNT 基因多态性与根尖周炎易感性。

WNT gene polymorphisms and predisposition to apical periodontitis.

机构信息

Department of Endodontics, University of Texas Health Science Center School of Dentistry, Houston, 77054, USA.

Center for Craniofacial Research, University of Texas Health Science Center School of Dentistry, Houston, 77054, USA.

出版信息

Sci Rep. 2019 Dec 12;9(1):18980. doi: 10.1038/s41598-019-55293-6.


DOI:10.1038/s41598-019-55293-6
PMID:31831777
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6908593/
Abstract

Single nucleotide polymorphisms (SNPs) in WNT genes may impact gene/protein function and contribute to individual predisposition to apical periodontitis (AP). Here, we investigated the association of SNPs in/nearby WNT3, WNT3A, WNT5A, WNT8A, WNT9B and WNT11 genes with AP using a case-control dataset. Cases were defined as individuals with deep caries and AP (n = 188); controls had deep caries and no AP (n = 230). Genotyping was performed using Taqman chemistry in real time PCR. Data analyses was performed using Fisher Exact tests assuming a Bonferroni correction threshold value of 0.005. Single-SNP association analysis revealed a trend for association with WNT3 rs9890413 genotypes (P = 0.009) under a dominant model and allelic association for WNT3A rs1745420 (P = 0.009). Haplotypes involving WNT3-WNT9B-WNT3A alleles were also significantly associated with AP (P ≤ 0.003). Luciferase reporter assays showed higher transcriptional activity (1.4-fold) with the alternate G allele in rs1745420. Expression of WNT3, WNT3A and WNT5A in AP tissues was significantly higher than in control tissues, and inversely correlated with the expression of SERPINB1, COL1A1 and TIMP1 (P < 0.05). Our results suggest that WNT genes have a role in modulating AP and polymorphisms in these genes may increase susceptibility to AP.

摘要

单核苷酸多态性(SNPs)在 WNT 基因中可能影响基因/蛋白质功能,并导致个体易患根尖周炎(AP)。在这里,我们使用病例对照数据集研究了 WNT3、WNT3A、WNT5A、WNT8A、WNT9B 和 WNT11 基因中的 SNPs 与 AP 的关联。病例定义为患有深龋和 AP 的个体(n=188);对照组为患有深龋且无 AP 的个体(n=230)。采用 Taqman 化学实时 PCR 进行基因分型。Fisher 精确检验用于数据分析,假设 Bonferroni 校正阈值为 0.005。单 SNP 关联分析显示,在显性模型下,WNT3 rs9890413 基因型与 AP 呈关联趋势(P=0.009),等位基因关联分析显示 WNT3A rs1745420 与 AP 呈关联趋势(P=0.009)。涉及 WNT3-WNT9B-WNT3A 等位基因的单倍型也与 AP 显著相关(P≤0.003)。荧光素酶报告基因检测显示,rs1745420 中的交替 G 等位基因具有更高的转录活性(1.4 倍)。AP 组织中 WNT3、WNT3A 和 WNT5A 的表达明显高于对照组,与 SERPINB1、COL1A1 和 TIMP1 的表达呈负相关(P<0.05)。我们的结果表明,WNT 基因在调节 AP 中起作用,这些基因中的多态性可能增加 AP 的易感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f65/6908593/10ba150ec53d/41598_2019_55293_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f65/6908593/8b47b7e7aa48/41598_2019_55293_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f65/6908593/10f045b2d055/41598_2019_55293_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f65/6908593/10ba150ec53d/41598_2019_55293_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f65/6908593/8b47b7e7aa48/41598_2019_55293_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f65/6908593/10f045b2d055/41598_2019_55293_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f65/6908593/10ba150ec53d/41598_2019_55293_Fig3_HTML.jpg

相似文献

[1]
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[3]
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[8]
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[9]
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引用本文的文献

[1]
Exploring the Influence of Genetic Single-Nucleotide Polymorphism (SNPs) on Endodontic Pathologies: A Comprehensive Review.

Cureus. 2024-11-25

[2]
Repopulation of a 3D simulated periapical lesion cavity with dental pulp stem cell spheroids with triggered osteoblastic differentiation.

Braz Dent J. 2024-12-16

[3]
Genome-wide Association Study Identifies Novel Risk Loci for Apical Periodontitis.

J Endod. 2023-10

[4]
Genome-wide association study identifies novel risk loci for apical periodontitis.

Res Sq. 2023-1-26

[5]
Genetic, Cellular and Molecular Aspects involved in Apical Periodontitis.

Braz Dent J. 2022

本文引用的文献

[1]
Interaction between the Wnt/β-catenin signaling pathway and the EMMPRIN/MMP-2, 9 route in periodontitis.

J Periodontal Res. 2018-6-14

[2]
Hypothesis-driven versus hypothesis-free approaches to the identification of genes for cleft lip and palate.

Arch Oral Biol. 2018-8

[3]
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Int Endod J. 2018-2-28

[4]
The effects of alternative splicing on miRNA binding sites in bladder cancer.

PLoS One. 2018-1-4

[5]
Dickkopf-1 may regulate bone coupling by attenuating wnt/β-catenin signaling in chronic apical periodontitis.

Arch Oral Biol. 2017-12-5

[6]
Proteomic Profiling and Differential Messenger RNA Expression Correlate HSP27 and Serpin Family B Member 1 to Apical Periodontitis Outcomes.

J Endod. 2017-6-30

[7]
Variants on chromosome 4q21 near PKD2 and SIBLINGs are associated with dental caries.

J Hum Genet. 2017-4

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Dent Clin North Am. 2017-1

[9]
Heat Shock 70 Protein Genes and Genetic Susceptibility to Apical Periodontitis.

J Endod. 2016-10

[10]
[Expression of Wnt5a in chronic apical periodontitis and its clinical significance].

Shanghai Kou Qiang Yi Xue. 2015-8

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