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了解癌症中的线粒体多态性。

Understanding Mitochondrial Polymorphisms in Cancer.

机构信息

Department of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.

Department of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, Pennsylvania.

出版信息

Cancer Res. 2017 Nov 15;77(22):6051-6059. doi: 10.1158/0008-5472.CAN-17-1939. Epub 2017 Nov 2.

Abstract

Alterations in mitochondrial DNA (mtDNA) were once thought to be predominantly innocuous to cell growth. Recent evidence suggests that mtDNA undergo naturally occurring alterations, including mutations and polymorphisms, which profoundly affect the cells in which they appear and contribute to a variety of diseases, including cardiovascular disease, diabetes, and cancer. Furthermore, interplay between mtDNA and nuclear DNA has been found in cancer cells, necessitating consideration of these complex interactions for future studies of cancer mutations and polymorphisms. In this issue of , Vivian and colleagues utilize a unique mouse model, called Mitochondrial Nuclear eXchange mice, that contain the nuclear DNA from one inbred mouse strain, and the mtDNA from a different inbred mouse strain to examine the genome-wide nuclear DNA methylation and gene expression patterns of brain tissue. Results demonstrated there were alterations in nuclear DNA expression and DNA methylation driven by mtDNA. These alterations may impact disease pathogenesis. In light of these results, in this review, we highlight alterations in mtDNA, with a specific focus on polymorphisms associated with cancer susceptibility and/or prognosis, mtDNA as cancer biomarkers, and considerations for investigating the role of mtDNA in cancer progression for future studies. .

摘要

线粒体 DNA(mtDNA)的改变曾被认为主要对细胞生长无害。最近的证据表明,mtDNA 会发生自然发生的改变,包括突变和多态性,这些改变会深刻影响其所在的细胞,并导致多种疾病,包括心血管疾病、糖尿病和癌症。此外,在癌细胞中发现了 mtDNA 和核 DNA 之间的相互作用,这就需要在未来的癌症突变和多态性研究中考虑这些复杂的相互作用。在本期 杂志中,Vivian 及其同事利用一种名为线粒体核交换(Mitochondrial Nuclear eXchange)的独特小鼠模型,该模型含有来自一种近交系小鼠的核 DNA 和来自另一种近交系小鼠的 mtDNA,来检测脑组织的全基因组核 DNA 甲基化和基因表达模式。结果表明,mtDNA 驱动了核 DNA 表达和 DNA 甲基化的改变。这些改变可能会影响疾病的发病机制。鉴于这些结果,在这篇综述中,我们重点介绍了 mtDNA 的改变,特别关注与癌症易感性和/或预后相关的多态性、作为癌症生物标志物的 mtDNA 以及未来研究中调查 mtDNA 在癌症进展中的作用的考虑因素。

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