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Mutations in AXIN2 gene as a risk factor for tooth agenesis and cancer: A review.

作者信息

Hlouskova Alena, Bielik Peter, Bonczek Ondrej, Balcar Vladimir J, Šerý Omar

机构信息

Laboratory of Neurobiology and Molecular Psychiatry, Department of Biochemistry, Faculty of Science, Masaryk University, Brno, Czech Republic.

Laboratory of Neurochemistry, Bosch Institute and Discipline of Anatomy and Histology, School of medical sciences, Sydney Medical School, The University of Sydney, 2006 Sydney, NSW, Australia.

出版信息

Neuro Endocrinol Lett. 2017 Jul;38(3):131-137.


DOI:
PMID:28759178
Abstract

AXIN2 gene plays a crucial role in morphogenesis of craniofacial area and is essential for tooth development. AXIN2 gene is one of the most studied genes associated with tooth agenesis, the most common defect of dentition in humans. Polymorphic variants in AXIN2 gene are discussed in relation to the occurrence of the tooth agenesis but also as an indication of the risk of cancer. Mutations in AXIN2 gene were found in patients with colorectal or hepatocellular carcinoma, prostate cancer, ovarium or lung cancer. These findings support the hypothesis that missing teeth may be a significant marker for predisposition for cancer.

摘要

相似文献

[1]
Mutations in AXIN2 gene as a risk factor for tooth agenesis and cancer: A review.

Neuro Endocrinol Lett. 2017-7

[2]
Tooth agenesis association with self-reported family history of cancer.

J Dent Res. 2012-11-20

[3]
Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis.

Arch Oral Biol. 2009-1

[4]
Genetic study of non-syndromic tooth agenesis through the screening of paired box 9, msh homeobox 1, axin 2, and Wnt family member 10A genes: a case-series.

Eur J Oral Sci. 2018-2

[5]
Functional analysis of a novel missense mutation in AXIN2 associated with non-syndromic tooth agenesis.

Eur J Oral Sci. 2016-6

[6]
Nonsyndromic oligodontia : Does the Tooth Agenesis Code (TAC) enable prediction of the causative mutation?

J Orofac Orthop. 2017-3

[7]
Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer.

Am J Hum Genet. 2004-5

[8]
PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia: a case-control study in southwest China.

J Appl Oral Sci. 2013

[9]
Familial colorectal cancer and tooth agenesis caused by an AXIN2 variant: how do we detect families with rare cancer predisposition syndromes?

Fam Cancer. 2022-7

[10]
[Association between AXIN2 polymorphism and oligodontia].

Beijing Da Xue Xue Bao Yi Xue Ban. 2014-4-18

引用本文的文献

[1]
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Int J Mol Sci. 2024-6-27

[2]
AXIN2-related oligodontia-colorectal cancer syndrome with cleft palate as a possible new feature.

Mol Genet Genomic Med. 2023-6

[3]
Tooth number abnormality: from bench to bedside.

Int J Oral Sci. 2023-1-6

[4]
WNT10A variants: following the pattern of inheritance in tooth agenesis and self-reported family history of cancer.

Clin Oral Investig. 2022-12

[5]
Short Linear Motifs Orchestrate Functioning of Human Proteins during Embryonic Development, Redox Regulation, and Cancer.

Metabolites. 2022-5-21

[6]
The nonredundant nature of the Axin2 regulatory network in the canonical Wnt signaling pathway.

Proc Natl Acad Sci U S A. 2022-3-1

[7]
Nonmalignant Features Associated with Inherited Colorectal Cancer Syndromes-Clues for Diagnosis.

Cancers (Basel). 2022-1-26

[8]
Evaluation of Classic, Attenuated, and Oligopolyposis of the Colon.

Gastrointest Endosc Clin N Am. 2022-1

[9]
Familial colorectal cancer and tooth agenesis caused by an AXIN2 variant: how do we detect families with rare cancer predisposition syndromes?

Fam Cancer. 2022-7

[10]
Association between tooth agenesis and cancer: a systematic review.

J Appl Oral Sci. 2021

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