Identification of sequence polymorphisms in the D-loop region of mitochondrial DNA as risk biomarkers for malignant fibrous histiocytoma.

Mitochondrial Dna Pub Date : 2015-06-01 Epub Date: 2013-10-01 DOI:10.3109/19401736.2013.836510
Jianjun Xun, Zhenxing Li, Xiaolei Song, Xueshi Wang
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引用次数: 5

Abstract

Single nucleotide polymorphisms (SNPs) in the mitochondrial DNA Displacement-loop (D-loop) region particularly in a highly polymorphic homopolymeric C stretch named D310 have been reported to be associated with cancer risk in several types of cancer. In order to evaluate the frequency of D-loop SNPs in a large series of malignant fibrous histiocytoma (MFH) and establish correlations with cancer risk, we sequenced the D-loop of 92 MFH patients and analyzed their use as predictive biomarkers for MFH risk. The minor alleles of nucleotides 73G, 151T were associated with an increased risk for MFH patients, whereas the alleles of nucleotides 16,298C, 152C, and insertion of C at the site 315 (located within the D310) were associated with a decreased risk for MFH patients. These results suggest that SNPs in the mitochondrial D-loop should be considered as a biomarker which may be useful for the early detection of MFH in individuals at risk of this cancer.

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鉴定线粒体DNA d环区序列多态性作为恶性纤维组织细胞瘤的风险生物标志物。
据报道,线粒体DNA位移环(D-loop)区域的单核苷酸多态性(snp),特别是在称为D310的高多态性同聚物C延伸段中,与几种癌症的癌症风险相关。为了评估大量恶性纤维组织细胞瘤(MFH)中d -环snp的频率并确定其与癌症风险的相关性,我们对92名MFH患者的d -环进行了测序,并分析了它们作为MFH风险预测生物标志物的用途。核苷酸73G、151T的次要等位基因与MFH患者的风险增加相关,而核苷酸16298c、152C和C插入315位点(位于D310内)的等位基因与MFH患者的风险降低相关。这些结果表明,线粒体d环中的snp应该被视为一种生物标志物,可能有助于早期检测MFH患者的癌症风险。
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Mitochondrial Dna
Mitochondrial Dna 生物-遗传学
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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.
期刊最新文献
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