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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.
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页码:333 / 337
页数:5
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