Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, 3501 Terrace Street, Pittsburgh, PA 15261, USA.
J Dent Res. 2013 Feb;92(2):149-55. doi: 10.1177/0022034512468750. Epub 2012 Nov 20.
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.
有人提出,牙齿缺失和癌症的发生可能共享共同的分子途径。我们进行了一项横断面研究,以调查牙齿缺失和自我报告的癌症家族史之间的流行病学和分子关联。从同一机构招募了 82 名牙齿缺失患者和 328 名无出生缺陷的个体。牙齿缺失在恒牙中进行评估,并根据参与者的年龄和初始牙齿形成时应在影像学上可见的时间来定义。我们还研究了参与牙发生的基因在肿瘤发生中的作用,对 AXIN2、FGF3、FGF10 和 FGFR2 中的 14 个标记物进行了基因分型。牙齿缺失患者有癌症家族史的风险增加(p=0.00006;OR=2.7;95%CI,1.6-4.4)。AXIN2、FGF3、FGF10 和 FGFR2 与牙齿缺失存在关联[即,携带 FGFR2 多态性等位基因(rs1219648)的个体发生前磨牙缺失的风险更高(p=0.02;OR=1.8;95%CI,1.1-3.0)]。总之,牙齿缺失与阳性自我报告的癌症家族史以及 AXIN2、FGF3、FGF10 和 FGFR2 的变异有关。需要前瞻性研究来证实牙齿缺失是否可以用作癌症的风险标志物。