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结直肠癌相关基因与牙齿缺失有关,可能在牙齿发育中起作用。

Colorectal Cancer-Associated Genes Are Associated with Tooth Agenesis and May Have a Role in Tooth Development.

机构信息

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

Department of Biological Sciences, University of Sao Paulo Bauru Dental School, Bauru, 17012, Brazil.

出版信息

Sci Rep. 2018 Feb 14;8(1):2979. doi: 10.1038/s41598-018-21368-z.


DOI:10.1038/s41598-018-21368-z
PMID:29445242
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5813178/
Abstract

Previously reported co-occurrence of colorectal cancer (CRC) and tooth agenesis (TA) and the overlap in disease-associated gene variants suggest involvement of similar molecular pathways. Here, we took an unbiased approach and tested genome-wide significant CRC-associated variants for association with isolated TA. Thirty single nucleotide variants (SNVs) in CRC-predisposing genes/loci were genotyped in a discovery dataset composed of 440 individuals with and without isolated TA. Genome-wide significant associations were found between TA and ATF1 rs11169552 (P = 4.36 × 10) and DUSP10 rs6687758 (P = 1.25 × 10), and positive association found with CASC8 rs10505477 (P = 8.2 × 10). Additional CRC marker haplotypes were also significantly associated with TA. Genotyping an independent dataset consisting of 52 cases with TA and 427 controls confirmed the association with CASC8. Atf1 and Dusp10 expression was detected in the mouse developing teeth from early bud stages to the formation of the complete tooth, suggesting a potential role for these genes and their encoded proteins in tooth development. While their individual contributions in tooth development remain to be elucidated, these genes may be considered candidates to be tested in additional populations.

摘要

先前有研究报道结直肠癌(CRC)和牙齿缺失(TA)的同时发生,以及疾病相关基因变异的重叠,这表明它们涉及相似的分子途径。在这里,我们采用一种无偏倚的方法,测试了与孤立性 TA 相关的全基因组显著 CRC 相关变异。在由 440 名有和没有孤立性 TA 的个体组成的发现数据集,对 30 个 CRC 易感基因/位点的单核苷酸变异(SNV)进行了基因分型。发现 TA 与 ATF1 rs11169552(P = 4.36×10)和 DUSP10 rs6687758(P = 1.25×10)之间存在全基因组显著关联,并且与 CASC8 rs10505477 存在正相关(P = 8.2×10)。其他 CRC 标记单体型也与 TA 显著相关。对包含 52 例 TA 患者和 427 例对照的独立数据集进行基因分型,证实了 CASC8 与 TA 的关联。在小鼠发育牙齿的早期芽阶段到完整牙齿形成阶段检测到 Atf1 和 Dusp10 的表达,表明这些基因及其编码蛋白在牙齿发育中可能发挥作用。虽然它们在牙齿发育中的个体贡献仍有待阐明,但这些基因可以被认为是在其他人群中进行测试的候选基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9520/5813178/486af2334cab/41598_2018_21368_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9520/5813178/a918b94953ba/41598_2018_21368_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9520/5813178/486af2334cab/41598_2018_21368_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9520/5813178/a918b94953ba/41598_2018_21368_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9520/5813178/486af2334cab/41598_2018_21368_Fig2_HTML.jpg

相似文献

[1]
Colorectal Cancer-Associated Genes Are Associated with Tooth Agenesis and May Have a Role in Tooth Development.

Sci Rep. 2018-2-14

[2]
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Int J Clin Exp Pathol. 2015-2-1

[3]
Genome-Wide Association and Transcriptome-Wide Association Studies Identify Novel Susceptibility Genes Contributing to Colorectal Cancer.

J Immunol Res. 2022

[4]
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Clin Genet. 2021-4

[5]
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J Dent Res. 2018-1-24

[6]
DUSP10 gene polymorphism and risk of colorectal cancer in the Han Chinese population.

Eur J Cancer Prev. 2014-5

[7]
A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12.

BMC Genomics. 2013-1-26

[8]
Correlation Between CASC8, SMAD7 Polymorphisms and the Susceptibility to Colorectal Cancer: An Updated Meta-Analysis Based on GWAS Results.

Medicine (Baltimore). 2015-11

[9]
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Mol Neurodegener. 2018-7-9

[10]
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Gastroenterology. 2018-12-6

引用本文的文献

[1]
Main genetic entities associated with tooth agenesis.

Clin Oral Investig. 2024-12-11

[2]
"Examining the link between tooth agenesis and papillary thyroid cancer: is there a risk factor?" Observational study.

Prog Orthod. 2024-3-25

[3]
Congenital Tooth Agenesis and Risk of Early-Onset Cancer.

JAMA Netw Open. 2024-3-4

[4]
Non-syndromic supernumerary teeth and association with a self-reported family history of cancer.

J Orofac Orthop. 2025-5

[5]
Transcriptomic Network Regulation of Rat Tooth Germ from Bell Differentiation Stage to Secretory Stage: MAPK Signaling Pathway Is Crucial to Extracellular Matrix Remodeling.

Biomed Res Int. 2023

[6]
Rethinking the Genetic Etiology of Nonsyndromic Tooth Agenesis.

Curr Osteoporos Rep. 2022-12

[7]
Association between tooth agenesis and cancer: a systematic review.

J Appl Oral Sci. 2021

[8]
Variations in predict risk and prognosis of colorectal cancer.

BDJ Open. 2019-10-16

[9]
Identification of Disease Risk DNA Variations is Shaping the Future of Precision Health.

Genes (Basel). 2019-6-13

[10]
The Dual-Specificity Phosphatase 10 (DUSP10): Its Role in Cancer, Inflammation, and Immunity.

Int J Mol Sci. 2019-4-1

本文引用的文献

[1]
Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis.

J Dent Res. 2018-1

[2]
Colorectal cancer population screening programs worldwide in 2016: An update.

World J Gastroenterol. 2017-5-28

[3]
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.

Nat Commun. 2017-2-24

[4]
The protein level and transcription activity of activating transcription factor 1 is regulated by prolyl isomerase Pin1 in nasopharyngeal carcinoma progression.

Cell Death Dis. 2016-12-29

[5]
Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation.

N Engl J Med. 2017-1-5

[6]
Mutations in WNT10B Are Identified in Individuals with Oligodontia.

Am J Hum Genet. 2016-7-7

[7]
Clinical Significance of Long Non-Coding RNA CASC8 rs10505477 Polymorphism in Lung Cancer Susceptibility, Platinum-Based Chemotherapy Response, and Toxicity.

Int J Environ Res Public Health. 2016-5-30

[8]
Hypodontia, a prospective predictive marker for tumor?

Oral Dis. 2016-5

[9]
Correlation Between CASC8, SMAD7 Polymorphisms and the Susceptibility to Colorectal Cancer: An Updated Meta-Analysis Based on GWAS Results.

Medicine (Baltimore). 2015-11

[10]
dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice-Site SNVs.

Hum Mutat. 2016-3

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