Understanding Mitochondrial Polymorphisms in Cancer

被引:35
作者
Bussard, Karen M. [1 ]
Siracusa, Linda D. [2 ]
机构
[1] Thomas Jefferson Univ, Dept Canc Biol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA
关键词
HEPATOCELLULAR-CARCINOMA; DNA METHYLATION; G10398A POLYMORPHISM; CERVICAL-CANCER; LOOP REGION; RISK-FACTOR; BREAST; ASSOCIATION; METASTASIS; 5-AZACYTIDINE;
D O I
10.1158/0008-5472.CAN-17-1939
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 Cancer Research, 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 genomewide 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. (C) 2017 AACR.
引用
收藏
页码:6051 / 6059
页数:9
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