Associations between Single Nucleotide Polymorphisms in the Mitochondrial DNA D-Loop Region and Outcome of Gastroenteropancreatic Neuroendocrine Neoplasm

被引:2
作者
Er, Li-Mian [1 ]
Li, Yong [2 ]
Er, Li [3 ]
Wu, MingLi [1 ]
Zheng, Xiu-li [1 ]
Guo, Zhan-jun [1 ]
Yuan, Hu-Fang [2 ]
机构
[1] Hebei Med Univ, Dept Endoscopy, Hosp 4, 12 Jian Kang Rd, Shijiazhuang 050011, Hebei, Peoples R China
[2] Hebei Med Univ, Hosp 4, Dept Surg 3, Shijiazhuang, Hebei, Peoples R China
[3] Youhao Hosp Yangzhou, Dept ICU, Yangzhou, Jiangsu, Peoples R China
关键词
Gastroenteropancreatic neuroendocrine neoplasm; SNPs; D-loop; mtDNA; Survival; NON-HODGKIN-LYMPHOMA; SEQUENCE POLYMORPHISMS; PROGNOSTIC-FACTORS; DISPLACEMENT LOOP; LUNG-CANCER; RISK-FACTOR; MUTATIONS; TUMORS; IDENTIFICATION;
D O I
暂无
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Accumulation of single-nucleotide polymorphisms (SNPs) in the displacement loop (D-loop) of mitochondrial DNA (mtDNA) may be associated with cancer risk and disease outcome. We evaluated the predictive value of these SNPs for GEP-NEN outcome. Three SNP sites of nucleotides16257C/A, 150C/T and 151C/Tdel were identified for statistically significant prediction of postoperative survival in GEP-NEN by univariate analysis with log-rank test. In addition, the minor haplotype of nucleotides 16257A in the hypervariable segment 1(HV1) region of the D-loop was identified for their association with lower survival rate of GEP-NEN (relative risk, 3.390; 95% CI, 1.071 similar to 10.729; p=0.038) by multivariate analysis with COX hazards model. The analysis of genetic polymorphisms in the mitochondrial D-loop can help identify patient subgroups with a high risk of GEP-NEN outcome.
引用
收藏
页码:333 / 337
页数:5
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