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线粒体 DNA 单倍群 M7 降低了中国北方汉族人群结直肠癌的发病风险。

Mitochondrial DNA haplogroup M7 confers a reduced risk of colorectal cancer in a Han population from northern China.

机构信息

Institute of Medical Research, Northwestern Polytechnical University, Xi'an, China.

State Key Laboratory of Cancer Biology and Department of Physiology and Pathophysiology, Fourth Military Medical University, Xi'an, China.

出版信息

J Cell Mol Med. 2021 Aug;25(15):7538-7544. doi: 10.1111/jcmm.16789. Epub 2021 Jul 19.

Abstract

Mitochondria are central eukaryotic organelles in cellular metabolism and ATP production. Mitochondrial DNA (mtDNA) alterations have been implicated in the development of colorectal cancer (CRC). However, there are few reports on the association between mtDNA haplogroups or single nucleotide polymorphisms (SNPs) and the risk of CRC. The mtDNA of 286 Northern Han Chinese CRC patients were sequenced by next-generation sequencing technology. MtDNA data from 811 Han Chinese population controls were collected from two public data sets. Then, logistic regression analysis was used to determine the effect of mtDNA haplogroup or SNP on the risk of CRC. We found that patients with haplogroup M7 exhibited a reduced risk of CRC when compared to patients with other haplogroups (odds ratio [OR] = 0.532, 95% confidence interval [CI] = 0.285-0.937, p = 0.036) or haplogroup B (OR = 0.477, 95% CI = 0.238-0.916, p = 0.030). Furthermore, haplogroup M7 was still associated with the risk of CRC when the validation and combined control cohort were used. In addition, several haplogroup M7 specific SNPs, including 199T>C, 4071C>T and 6455C>T, were significantly associated with the risk of CRC. Our results indicate the risk potential of mtDNA haplogroup M7 and SNPs in CRC in Northern China.

摘要

线粒体是细胞代谢和 ATP 产生的中心真核细胞器。线粒体 DNA(mtDNA)改变与结直肠癌(CRC)的发展有关。然而,关于 mtDNA 单倍群或单核苷酸多态性(SNP)与 CRC 风险之间的关联的报道很少。通过下一代测序技术对 286 例北方汉族 CRC 患者的 mtDNA 进行测序。从两个公共数据集收集了 811 名汉族人口对照的 mtDNA 数据。然后,使用逻辑回归分析确定 mtDNA 单倍群或 SNP 对 CRC 风险的影响。我们发现,与具有其他单倍群的患者相比,具有单倍群 M7 的患者 CRC 风险降低(比值比 [OR] = 0.532,95%置信区间 [CI] = 0.285-0.937,p = 0.036)或单倍群 B(OR = 0.477,95%CI = 0.238-0.916,p = 0.030)。此外,当使用验证和合并对照队列时,单倍群 M7 仍与 CRC 的风险相关。此外,几个单倍群 M7 特异性 SNP,包括 199T>C、4071C>T 和 6455C>T,与 CRC 风险显著相关。我们的研究结果表明 mtDNA 单倍群 M7 和 SNPs 在华北地区 CRC 中的风险潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7473/8335663/f57911d3a4d2/JCMM-25-7538-g001.jpg

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