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[Epidemiological characteristics of gastric cancer in China, 2015].[2015年中国胃癌的流行病学特征]
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2
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DNA Cell Biol. 2020 Aug;39(8):1385-1400. doi: 10.1089/dna.2019.5220. Epub 2020 Jan 16.
3
Mitochondrial Dysfunction in Aging and Cancer.衰老与癌症中的线粒体功能障碍
J Clin Med. 2019 Nov 15;8(11):1983. doi: 10.3390/jcm8111983.
4
Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.全球癌症统计数据 2018:GLOBOCAN 对全球 185 个国家/地区 36 种癌症的发病率和死亡率的估计。
CA Cancer J Clin. 2018 Nov;68(6):394-424. doi: 10.3322/caac.21492. Epub 2018 Sep 12.
5
Cytochrome c oxidase deficiency, oxidative stress, possible antioxidant therapy and link to nuclear DNA damage.细胞色素 c 氧化酶缺乏、氧化应激、可能的抗氧化治疗与核 DNA 损伤的关系。
Eur J Hum Genet. 2018 Apr;26(4):579-581. doi: 10.1038/s41431-017-0047-5. Epub 2018 Feb 2.
6
Identification of sequence polymorphisms in the mitochondrial cytochrome c oxidase genes as risk factors for hepatocellular carcinoma.线粒体细胞色素c氧化酶基因序列多态性作为肝细胞癌危险因素的鉴定。
J Clin Lab Anal. 2018 Mar;32(3). doi: 10.1002/jcla.22299. Epub 2017 Jul 13.
7
Mitochondrial Genomic Backgrounds Affect Nuclear DNA Methylation and Gene Expression.线粒体基因组背景影响核DNA甲基化和基因表达。
Cancer Res. 2017 Nov 15;77(22):6202-6214. doi: 10.1158/0008-5472.CAN-17-1473. Epub 2017 Jun 29.
8
Genome-wide analysis of DNA copy number alterations in early and advanced gastric cancers.早期和进展期胃癌DNA拷贝数改变的全基因组分析。
Mol Carcinog. 2017 Feb;56(2):527-537. doi: 10.1002/mc.22514. Epub 2016 Aug 24.
9
Identification of sequence polymorphisms in the D-Loop region of mitochondrial DNA as a risk factor for colon cancer.线粒体DNA D环区域序列多态性作为结肠癌危险因素的鉴定。
Mitochondrial DNA A DNA Mapp Seq Anal. 2016 Nov;27(6):4244-4245. doi: 10.3109/19401736.2014.1003920. Epub 2016 May 20.
10
Single nucleotide polymorphisms in the mitochondrial displacement loop and age-at-onset of familial breast cancer.线粒体置换环中的单核苷酸多态性与家族性乳腺癌的发病年龄
Mitochondrial DNA A DNA Mapp Seq Anal. 2016 Sep;27(5):3082-5. doi: 10.3109/19401736.2014.1003918.

线粒体细胞色素c氧化酶基因多态性作为胃癌危险因素的鉴定。

Identification of polymorphisms in mitochondrial cytochrome c oxidase genes as risk factors for gastric cancer.

作者信息

Wang Yingnan, Wang Hongcai, Yin Shice, Zhang Jingjing, Zhang Ruixing, Guo Zhanjun

机构信息

Department of Gastroenterology and Hepatology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.

Department of Intensive-care Unit, The Xingtai People's Hospital, Xingtai, China.

出版信息

Transl Cancer Res. 2020 Jun;9(6):3854-3859. doi: 10.21037/tcr-19-2227.

DOI:10.21037/tcr-19-2227
PMID:35117752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8799121/
Abstract

BACKGROUND

Single nucleotide polymorphisms (SNPs) in the D-Loop region of mitochondrial DNA (mtDNA) have been implied in tumorigenesis of different types of tumors, but the associations involving polymorphisms in mtDNA coding regions still need to be clarified. This study aimed to identify SNPs of mitochondrial cytochrome c oxidase genes (MT-CO) in the occurrence of gastric cancer (GC).

METHODS

The MT-CO genes were sequenced between 170 GC patients and 174 matched healthy controls. The test was used to analyze differences in SNP frequencies between the two groups.

RESULTS

The SNPs of MT-CO region were associated with the risk of GC. The genotype 9540T was significantly associated with an increased risk for GC (P=0.018), whereas 9548G was associated with a reduced risk (P=0.029).

CONCLUSIONS

The SNPs in MT-CO genes were found to be risk biomarkers for GC. It may provide a novel insight into the molecular mechanism in GC tumorigenesis and progression.

摘要

背景

线粒体DNA(mtDNA)D环区域的单核苷酸多态性(SNP)已被认为与不同类型肿瘤的发生有关,但mtDNA编码区域多态性的相关情况仍有待阐明。本研究旨在确定线粒体细胞色素c氧化酶基因(MT-CO)的SNP在胃癌(GC)发生中的作用。

方法

对170例GC患者和174例匹配的健康对照者的MT-CO基因进行测序。采用检验分析两组间SNP频率的差异。

结果

MT-CO区域的SNP与GC风险相关。基因型9540T与GC风险增加显著相关(P=0.018),而9548G与风险降低相关(P=0.029)。

结论

发现MT-CO基因中的SNP是GC的风险生物标志物。这可能为GC发生和发展的分子机制提供新的见解。