Journal of dental research · 2012
Tooth agenesis association with self-reported family history of cancer.
Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Küchler E C, Lips A, Tannure P N, Ho B, Costa M C, Granjeiro J M, Vieira A R
Аннотация
It has been proposed that tooth agenesis and cancer development share common molecular pathways. We performed a cross-sectional study to investigate the epidemiological and molecular association between tooth agenesis and self-reported family history of cancer. Eighty-two individuals with tooth agenesis and 328 individuals with no birth defect were recruited from the same institution. Tooth agenesis was assessed in permanent teeth and was defined based on the age of the participants and when initial tooth formation should be radiographically visible. We also investigated the role of genes involved in dental development that have been implicated in tumorigenesis, and 14 markers in AXIN2, FGF3, FGF10, and FGFR2 were genotyped. Individuals with tooth agenesis had an increased risk of having a family history of cancer (p = 0.00006; OR = 2.7; 95% C.I., 1.6-4.4). There were associations between AXIN2, FGF3, FGF10, and FGFR2 with tooth agenesis [i.e., individuals who carried the polymorphic allele of FGFR2 (rs1219648) presented higher risk for having premolar agenesis (p = 0.02; OR = 1.8; 95% C.I., 1.1-3.0)]. In conclusion, tooth agenesis was associated with positive self-reported family history of cancer and with variants in AXIN2, FGF3, FGF10, and FGFR2. Prospective studies are needed to confirm if tooth agenesis can be used as a risk marker for cancer.
Предметные рубрики MeSH
AllelesAnodontiaAxin ProteinBicuspidBrazilBreast NeoplasmsCase-Control StudiesCross-Sectional StudiesEpidemiologic StudiesFemaleFibroblast Growth Factor 10Fibroblast Growth Factor 3Genetic VariationGenotypeHumansIncisorMaleMolecular EpidemiologyNeoplasmsOdontogenesisPolymorphism, GeneticProstatic NeoplasmsReceptor, Fibroblast Growth Factor, Type 2Risk FactorsSelf Report