Literature DB >> 29226748

Epigenetic biomarkers: Current strategies and future challenges for their use in the clinical laboratory.

José Luis García-Giménez1,2,3,4,5, Marta Seco-Cervera1,2,3, Trygve O Tollefsbol6, Carlos Romá-Mateo1,2,3,4, Lorena Peiró-Chova2,7, Pablo Lapunzina1,8, Federico V Pallardó1,2,3,4.   

Abstract

Epigenetic modifications and regulators represent potential molecular elements which control relevant physiological and pathological features, thereby contributing to the natural history of human disease. These epigenetic modulators can be employed as disease biomarkers, since they show several advantages and provide information about gene function, thus explaining differences among patient endophenotypes. In addition, epigenetic biomarkers can incorporate information regarding the effects of the environment and lifestyle on health and disease, and monitor the effect of applied therapies. Technologies used to analyze these epigenetic biomarkers are constantly improving, becoming much easier to use. Laboratory professionals can easily acquire experience and techniques are becoming more affordable. A high number of epigenetic biomarker candidates are being continuously proposed, making now the moment to adopt epigenetics in the clinical laboratory and convert epigenetic marks into reliable biomarkers. In this review, we describe some current promising epigenetic biomarkers and technologies being applied in clinical practice. Furthermore, we will discuss some laboratory strategies and kits to accelerate the adoption of epigenetic biomarkers into clinical routine. The likelihood is that over time, better markers will be identified and will likely be incorporated into future multi-target assays that might help to optimize its application in a clinical laboratory. This will improve cost-effectiveness, and consequently encourage the development of theragnosis and the application of precision medicine.

Entities:  

Keywords:  DNA methylation; Epigenetic biomarkers; histone postranslational modifications; miRNAs

Mesh:

Substances:

Year:  2017        PMID: 29226748      PMCID: PMC6733278          DOI: 10.1080/10408363.2017.1410520

Source DB:  PubMed          Journal:  Crit Rev Clin Lab Sci        ISSN: 1040-8363            Impact factor:   6.250


  144 in total

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