Ning Lifeng, Rao Wenwang, Yu Yaqin, Liu Xiaoli, Pan Yuchen, Ma Yuan, Liu Rui, Zhang Shangchao, Sun Hui, Yu Qiong
Department of Epidemiology and Biostatistics, School of Public Health, Jilin University, Changchun, Jilin Province, China.; National Research Institute for Family Planning, Beijing, China.
Department of Epidemiology and Biostatistics, School of Public Health, Jilin University, Changchun, Jilin Province, China.
J Cancer. 2016 Dec 9;7(15):2420-2426. doi: 10.7150/jca.16507. eCollection 2016.
Several studies have reported the association between MAPK signaling pathway gene polymorphisms and papillary thyroid carcinoma (PTC). gene, an oncogene from the mammalian gene family plays an important role in the MAPK pathway. This study aimed to identify the potential association of gene polymorphisms with susceptibility to PTC in a Han Chinese population. A total of 861 patients with PTC, 562 disease controls with nodular goiter and 897 healthy controls were recruited. Four tagSNP polymorphisms (rs12427141, rs712, rs7315339 and rs7960917) of gene were genotyped by matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF-MS) Statistical analyses and haplotype estimations were conducted using Haploview and Unphased softwares. Only significant differences were observed in genotypic frequencies of the rs7315339 polymorphism (χ =7.234, df=2, p=0.027) between PTC and disease controls. Statistically significant differences in both allelic and genotypic genotypes frequencies for rs712 (Genotype, χ=8.258, p=0.016) and rs12427141 (Allele, χ=3.992, p=0.046; Genotype, χ=8.140, p=0.017) were observed between PTC patients and controls. Haplotype analyses revealed higher frequencies of GA and TA haplotypes (p=0.039 and p=0.003, respectively) from rs712- rs12427141 (two-SNP) or TGA and TTG haplotype containing the alleles from rs7960917, rs712 and rs12427141, as well as the GAT haplotype containing the alleles from rs712, rs12427141 and rs7315339 in PTC patients than in healthy controls (p=0.042, p=0.037, p=0.027, respectively). Inversely, the haplotype TTA from rs7960917, rs712 and rs12427141 or the haplotype TAC from rs712, rs12427141 and rs7315339 was significantly less frequent in the PTC patients than in normal control (p=0.003, p=0.003, respectively). These findings suggest the role of these gene variants in susceptibility to PTC. Moreover, significant differences of the gene polymorphisms may occur between nodular goiter and PTC.
多项研究报道了丝裂原活化蛋白激酶(MAPK)信号通路基因多态性与甲状腺乳头状癌(PTC)之间的关联。 基因是哺乳动物 基因家族中的一个癌基因,在MAPK通路中起重要作用。本研究旨在确定汉族人群中 基因多态性与PTC易感性之间的潜在关联。共招募了861例PTC患者、562例结节性甲状腺肿疾病对照者和897例健康对照者。通过基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-MS)对 基因的四个标签单核苷酸多态性(tagSNP,rs12427141、rs712、rs7315339和rs7960917)进行基因分型。使用Haploview和Unphased软件进行统计分析和单倍型估计。仅在rs7315339多态性的基因型频率上观察到PTC与疾病对照之间存在显著差异(χ =7.234,自由度=2,p=0.027)。在PTC患者与对照之间,观察到rs712(基因型,χ=8.258,p=0.016)和rs12427141(等位基因,χ=3.992,p=0.046;基因型,χ=8.140,p=0.017)的等位基因和基因型频率存在统计学显著差异。单倍型分析显示,与健康对照相比,PTC患者中rs712-rs12427141(双SNP)的GA和TA单倍型(分别为p=0.039和p=0.003)、包含rs7960917、rs712和rs12427141等位基因的TGA和TTG单倍型以及包含rs712、rs12427141和rs7315339等位基因的GAT单倍型频率更高(分别为p=0.042、p=0.037、p=0.027)。相反,rs7960917、rs712和rs12427141的TTA单倍型或rs712、rs12427141和rs7315339的TAC单倍型在PTC患者中的频率显著低于正常对照(分别为p=0.003、p=0.003)。这些发现提示这些 基因变异在PTC易感性中的作用。此外,结节性甲状腺肿和PTC之间 基因多态性可能存在显著差异。