Single nucleotide polymorphisms in the D-loop region of mitochondrial DNA is associated with renal cell carcinoma outcome

被引:10
|
作者
Bai, Yaling [1 ]
Guo, Zhanjun [2 ]
Xu, Jinsheng [1 ]
Liu, Shufeng [3 ]
Zhang, Junxia [1 ]
Cui, Liwen [1 ]
Zhang, Huiran [1 ]
Zhang, Shenglei [1 ]
机构
[1] Hebei Med Univ, Hosp 4, Dept Nephrol, Shijiazhuang 050011, Peoples R China
[2] Hebei Med Univ, Hosp 4, Dept Gastroenterol & Hepatol, Shijiazhuang 050011, Peoples R China
[3] Hebei Med Univ, Hebei Key Lab Lab Anim, Shijiazhuang, Peoples R China
来源
MITOCHONDRIAL DNA | 2015年 / 26卷 / 02期
关键词
D-loop; mtDNA; outcome; renal cell carcinoma; SNP; OXIDATIVE STRESS; RISK-FACTOR; CANCER; IDENTIFICATION; TRANSCRIPTION; MUTATIONS; GENOME;
D O I
10.3109/19401736.2013.825772
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:224 / 226
页数:3
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