MicroRNAs as Peripheral Biomarkers in Aging and Age-Related Diseases

被引:172
作者
Kumar, S. [1 ]
Vijayan, M. [1 ]
Bhatti, J. S. [1 ,2 ]
Reddy, P. H. [1 ,3 ]
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Garrison Inst Aging, Lubbock, TX 79430 USA
[2] Sri Guru Gobind Singh Coll, Dept Biotechnol, Chandigarh, India
[3] Texas Tech Univ, Hlth Sci Ctr, Lubbock, TX 79430 USA
来源
MOLECULAR BIOLOGY OF AGING | 2017年 / 146卷
关键词
CIRCULATING MICRORNAS; POTENTIAL BIOMARKERS; ALZHEIMERS-DISEASE; SERUM MICRORNAS; EARLY-DIAGNOSIS; PLASMA; EXPRESSION; MIRNAS; IDENTIFICATION; CELLS;
D O I
10.1016/bs.pmbts.2016.12.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) are found in the circulatory biofluids considering the important molecules for biomarker study in aging and age-related diseases. Blood or blood components (serum/plasma) are primary sources of circulatory miRNAs and can release these in cell-free form either bound with some protein components or encapsulated with microvesicle particles, called exosomes. miRNAs are quite stable in the peripheral circulation and can be detected by high-throughput techniques like qRT-PCR, microarray, and sequencing. Intracellular miRNAs could modulate mRNA activity through target-specific binding and play a crucial role in intercellular communications. At a pathological level, changes in cellular homeostasis lead to the modulation of molecular function of cells; as a result, miRNA expression is deregulated. Deregulated miRNAs came out from cells and frequently circulate in extracellular body fluids as part of various human diseases. Most common aging-associated diseases are cardiovascular disease, cancer, arthritis, dementia, cataract, osteoporosis, diabetes, hypertension, and neurodegenerative diseases such as Alzheimer's disease, Huntington's disease, Parkinson's disease, and amyotrophic lateral sclerosis. Variation in the miRNA signature in a diseased peripheral circulatory system opens up a new avenue in the field of biomarker discovery. Here, we measure the biomarker potential of circulatory miRNAs in aging and various aging-related pathologies. However, further more confirmatory researches are needed to elaborate these findings at the translation level.
引用
收藏
页码:47 / 94
页数:48
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