Mutations in AXIN2 gene as a risk factor for tooth agenesis and cancer: A review
Jazyk angličtina Země Švédsko Médium print
Typ dokumentu časopisecké články, přehledy
PubMed
28759178
PII: NEL380317R01
Knihovny.cz E-zdroje
- MeSH
- anodoncie genetika MeSH
- axin protein genetika MeSH
- genetická predispozice k nemoci MeSH
- genotyp MeSH
- lidé MeSH
- mutace MeSH
- nádory genetika MeSH
- polymorfismus genetický MeSH
- rizikové faktory MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- axin protein MeSH
- AXIN2 protein, human MeSH Prohlížeč
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.