线粒体DNA d环区域的单核苷酸多态性与肾细胞癌的预后有关。

Mitochondrial Dna Pub Date : 2015-04-01 Epub Date: 2013-09-11 DOI:10.3109/19401736.2013.825772
Yaling Bai, Zhanjun Guo, Jinsheng Xu, Shufeng Liu, Junxia Zhang, Liwen Cui, Huiran Zhang, Shenglei Zhang
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引用次数: 12

摘要

线粒体DNA (mtDNA)位移环(d环)中单核苷酸多态性(snp)的积累已在各种类型的癌症中得到描述,并可能与癌症风险和疾病结局相关。我们在之前的病例对照研究中发现了14个snp频率高于5%,5个snp与肾细胞癌(RCC)的风险相关。在本研究中,我们评估了这些SNP与RCC患者预后的关系,通过对数秩检验确定了262C/T的SNP,对RCC生存的预测具有统计学意义。在整体多变量分析中,等位基因262被确定为RCC预后的独立预测因子。262T患者的生存时间明显短于262C患者(相对危险度,2.136,95%CI, 1.863-2.449;P = 0.000)。对线粒体d环遗传多态性的分析可以帮助确定疾病预后不良的高风险患者亚组。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Single nucleotide polymorphisms in the D-loop region of mitochondrial DNA is associated with renal cell carcinoma outcome.

Accumulation of single nucleotide polymorphisms (SNPs) in the displacement loop (D-loop) of mitochondrial DNA (mtDNA) has been described in various types of cancers and might be associated with cancer risk and disease outcome. We identified 14 SNPs with a frequency higher than 5% and 5 SNPs associated with the risk of renal cell carcinoma (RCC) in a case-control study previously. In the present study, we assessed the relationship of these SNPs and the outcome of RCC patients, a SNP of 262C/T was identified by the log-rank test for statistically significant prediction of RCC survival. In an overall multivariate analysis, allele 262 was identified as an independent predictor of RCC outcome. The length of survival of patients with 262T was significantly shorter than that of patients with allele 262C (relative risk, 2.136, 95%CI, 1.863-2.449; p = 0.000). The analysis of genetic polymorphisms in the mitochondrial D-loop can help identify patients subgroup at high risk of a poor disease outcome.

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来源期刊
Mitochondrial Dna
Mitochondrial Dna 生物-遗传学
自引率
0.00%
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0
审稿时长
2.4 months
期刊介绍: Previously published under the title DNA Sequence (Vols 1-19.3), Mitochondrial DNA accepts original high-quality reports based on mapping, sequencing and analysis of mitochondrial DNA and RNA. Descriptive papers on DNA sequences from mitochondrial genomes, and also analytical papers in the areas of population genetics, medical genetics, phylogenetics and human evolution that use mitochondrial DNA as a source of evidence for studies will be considered for publication. The editorial board will also consider manuscripts that examine population genetic and systematic theory that specifically address the use of mitochondrial DNA sequences.
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