DNA Methylation Biomarkers: Cancer and Beyond

被引:191
|
作者
Mikeska, Thomas [1 ]
Craig, Jeffrey M. [2 ,3 ]
机构
[1] Genet Technol Ltd, Fitzroy, Vic 3065, Australia
[2] Royal Childrens Hosp, Murdoch Childrens Res Inst, Parkville, Vic 3052, Australia
[3] Univ Melbourne, Dept Paediat, Parkville, Vic 3052, Australia
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
cancer; diabetes; obesity; smoking; stress; autism; schizophrenia; bipolar disorder; depression; environmental factors; MGMT PROMOTER METHYLATION; EPIGENOME-WIDE ASSOCIATION; GLUCOCORTICOID-RECEPTOR GENE; POLYMERASE-CHAIN-REACTION; DEPENDENT PROBE AMPLIFICATION; SEROTONIN TRANSPORTER GENE; POSITIVE BREAST-CANCER; LIPID-LOWERING DRUGS; TIME PCR ASSAY; CPG-ISLANDS;
D O I
10.3390/genes5030821
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Biomarkers are naturally-occurring characteristics by which a particular pathological process or disease can be identified or monitored. They can reflect past environmental exposures, predict disease onset or course, or determine a patient's response to therapy. Epigenetic changes are such characteristics, with most epigenetic biomarkers discovered to date based on the epigenetic mark of DNA methylation. Many tissue types are suitable for the discovery of DNA methylation biomarkers including cell-based samples such as blood and tumor material and cell-free DNA samples such as plasma. DNA methylation biomarkers with diagnostic, prognostic and predictive power are already in clinical trials or in a clinical setting for cancer. Outside cancer, strong evidence that complex disease originates in early life is opening up exciting new avenues for the detection of DNA methylation biomarkers for adverse early life environment and for estimation of future disease risk. However, there are a number of limitations to overcome before such biomarkers reach the clinic. Nevertheless, DNA methylation biomarkers have great potential to contribute to personalized medicine throughout life. We review the current state of play for DNA methylation biomarkers, discuss the barriers that must be crossed on the way to implementation in a clinical setting, and predict their future use for human disease.
引用
收藏
页码:821 / 864
页数:44
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