Guo Zhanjun, Yang Hua, Zhang Fengbin, Zhang Ruixing, Wang Cuiju
Department of Gastroenterology and Hepatology, The Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, P.R. China.
Oncol Lett. 2012 Feb;3(2):482-484. doi: 10.3892/ol.2011.494. Epub 2011 Nov 25.
The accumulation of single nucleotide polymorphisms (SNPs) in the displacement loop (D-loop) of mitochondrial DNA (mtDNA) has been described for various types of cancer, and their association with cancer risk and disease outcome has been extensively identified. In the present study, we investigated the association between age-at-onset and SNPs in the mitochondrial D-loop using a population-based series of esophageal squamous cell carcinoma (ESCC) patients. The SNP sites of nucleotides 16266 C/T were identified for their association with age-at-onset using the log-rank test. The age-at-onset of patients with the minor allele T genotype was significantly lower than that of patients with the C genotype at the 16266 site (p=0.036). Genetic polymorphisms in the D-loop are predictive markers for age-at-onset in ESCC patients. Accordingly, the analysis of genetic polymorphisms in the mitochondrial D-loop may help identify ESCC patient subgroups at high risk of early onset.
线粒体DNA(mtDNA)置换环(D-loop)中单个核苷酸多态性(SNP)的积累已在多种类型的癌症中被描述,并且它们与癌症风险和疾病预后的关联也已被广泛确定。在本研究中,我们使用基于人群的一系列食管鳞状细胞癌(ESCC)患者,研究了线粒体D-loop中SNP与发病年龄之间的关联。使用对数秩检验确定核苷酸16266 C/T的SNP位点与发病年龄的关联。在16266位点,携带次要等位基因T基因型患者的发病年龄显著低于携带C基因型的患者(p = 0.036)。D-loop中的基因多态性是ESCC患者发病年龄的预测标志物。因此,分析线粒体D-loop中的基因多态性可能有助于识别早发风险高的ESCC患者亚组。